Chisso Corporation

Japan

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IPC Class
C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings 35
G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells 33
C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls 30
C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters 25
C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring 24
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Status
Pending 2
Registered / In Force 64
Found results for  patents

1.

Method of storing thermoresponsive polymer in state of aqueous solution

      
Application Number 13149545
Grant Number 08105503
Status In Force
Filing Date 2011-05-31
First Publication Date 2011-09-29
Grant Date 2012-01-31
Owner Chisso Corporation (Japan)
Inventor
  • Eguchi, Masaru
  • Ohnishi, Noriyuki

Abstract

It is intended to provide an aqueous solution of a thermoresponsive polymer, which shows an upper critical solution temperature (UCST) and is capable of maintaining a dissolved state, even if it is stored for a long period of time at a temperature at which a ligand such as an antibody or an antigen is not inactivated. A UCST lowering agent is incorporated in a predetermined amount in an aqueous solution of a thermoresponsive polymer which shows a UCST in a state of containing water, thereby lowering the UCST of the aqueous solution to less than the storage temperature, and the resulting aqueous solution is stored.

IPC Classes  ?

2.

THERMOSETTING COMPOSITION

      
Application Number 12883453
Status Pending
Filing Date 2010-09-16
First Publication Date 2011-04-21
Owner CHISSO CORPORATION (Japan)

Abstract

A material of cured film, a thermosetting film and a display device are provided. The thermosetting composition includes a solvent and at least one siloxane polymer selected from the group consisting of siloxane polymer (A) obtained by hydrolyzing or condensing a silane mixture containing a mono functional silane represented by formula (1) and a trifunctional silane represented by formula (2), and siloxane polymer (B) obtained by hydrolyzing or condensing a silane mixture containing a bifunctional silane represented by formula (3) and a tetrafunctional silane represented by formula (4). A material of cured film, a thermosetting film and a display device are provided. The thermosetting composition includes a solvent and at least one siloxane polymer selected from the group consisting of siloxane polymer (A) obtained by hydrolyzing or condensing a silane mixture containing a mono functional silane represented by formula (1) and a trifunctional silane represented by formula (2), and siloxane polymer (B) obtained by hydrolyzing or condensing a silane mixture containing a bifunctional silane represented by formula (3) and a tetrafunctional silane represented by formula (4). A material of cured film, a thermosetting film and a display device are provided. The thermosetting composition includes a solvent and at least one siloxane polymer selected from the group consisting of siloxane polymer (A) obtained by hydrolyzing or condensing a silane mixture containing a mono functional silane represented by formula (1) and a trifunctional silane represented by formula (2), and siloxane polymer (B) obtained by hydrolyzing or condensing a silane mixture containing a bifunctional silane represented by formula (3) and a tetrafunctional silane represented by formula (4). R independently represents hydrogen, an alkyl group having 1 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, an aryl group having 6 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, or an alkenyl group having 2 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen. R′ independently represents a hydrolyzable group.

IPC Classes  ?

  • B32B 25/20 - Layered products essentially comprising natural or synthetic rubber comprising silicone rubber
  • C08L 83/06 - Polysiloxanes containing silicon bound to oxygen-containing groups

3.

Polymerizable liquid crystal composition and polymer thereof

      
Application Number 12613381
Grant Number RE042221
Status In Force
Filing Date 2009-11-05
First Publication Date 2011-03-15
Grant Date 2011-03-15
Owner
  • Chisso Corporation (Japan)
  • Chisso Petrochemical Corporation (Japan)
Inventor
  • Ito, Maiko
  • Kimura, Masami
  • Shundo, Ryushi

Abstract

the polymerizable liquid crystal composition having homogeneous, homeotropic, or hybrid alignment, which can be coated on a support substrate, for example, of a transparent plastic film such as a triacetyl cellulose film or cycloolefin polymer film, or glass, and is aligned on a substrate as a polymer film while maintaining the alignment.

IPC Classes  ?

  • C09K 19/38 - Polymers, e.g. polyamides
  • C09K 19/54 - Additives having no specific mesophase
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C07C 25/24 - Halogenated aromatic hydrocarbons with unsaturated side chains
  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C07C 69/76 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring

4.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009064749
Publication Number 2010/032587
Status In Force
Filing Date 2009-08-25
Publication Date 2010-03-25
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Saito Masayuki
  • Hattori Norikatsu

Abstract

Disclosed is a liquid crystal composition which satisfies at least one of such characteristics as high upper limit temperature of the nematic phase, low lower limit temperature of the nematic phase, low viscosity, adequate optical anisotropy, large negative dielectric anisotropy, high resistivity, high stability against ultraviolet light and high stability against heat, or has an adequate balance between at least two of the above-mentioned characteristics.  Also disclosed is an AM element having a short response time, high voltage holding ratio, high contrast ratio, long life and the like. The liquid crystal composition contains a specific compound having 1-pyran-2,5-diyl as a first component, and a specific compound having a large negative dielectric anisotropy as a second component, and has a negative dielectric anisotropy.  A liquid crystal display element contains the composition.

IPC Classes  ?

  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

5.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009065288
Publication Number 2010/032612
Status In Force
Filing Date 2009-09-02
Publication Date 2010-03-25
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Hattori Norikatsu
  • Saito Masayuki
  • Kawasaki Subaru
  • Fujita Hiroaki

Abstract

Disclosed is a liquid crystal composition that can satisfy at least one of properties such as a high upper limit temperature of a nematic phase, a low lower limit temperature of a nematic phase, a low viscosity, a proper optical anisotropy, a negatively high permittivity anisotropy, a high specific resistance, a high stability against ultraviolet light, and a high stability against heat, or has a proper balance between at least two of the above properties.  Also disclosed is a liquid crystal display element such as an AM element having a short response time, a high voltage retention, a high contrast ratio, and a prolonged service life. The liquid crystal composition comprises a first component of a dicyclic compound which has a negatively high permittivity anisotropy and contains fluorine at at least three of lateral positions, a second component of a specific dicyclic compound or a tricyclic compound having a pyran ring, a third component of a specific compound having a low viscosity, and a fourth component of a specific compound having a negatively high permittivity anisotropy and contains a negative permittivity anisotropy.  The liquid crystal display element comprises the composition.

IPC Classes  ?

  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

6.

HIGH-PURITY CRYSTALLINE SILICON, HIGH-PURITY SILICON TETRACHLORIDE, AND PROCESSES FOR PRODUCING SAME

      
Application Number JP2009065485
Publication Number 2010/029894
Status In Force
Filing Date 2009-09-04
Publication Date 2010-03-18
Owner
  • CHISSO CORPORATION (Japan)
  • JX Nippon Mining & Metals Corporation (Japan)
  • TOHO TITANIUM CO., LTD. (Japan)
Inventor
  • Hayashida, Satoshi
  • Kato, Wataru

Abstract

Provided are: high-purity crystalline silicon which is more inexpensive and can satisfy not only the quality requirements for a raw material for silicon for solar cells but also part of the quality requirements for silicon for the latest semiconductors; a process for producing the crystalline silicon; high-purity silicon tetrachloride for use in producing high-purity crystalline silicon; and a process for producing the silicon tetrachloride.  The high-purity crystalline silicon has a boron content of 0.015 ppm by weight or lower and a zinc content of 50-1,000 ppb by weight.  The process for producing high-purity crystalline silicon is characterized by feeding silicon tetrachloride gas and zinc gas to a vertical reactor, reacting the gases at 800-1,200ºC to thereby yield crude crystalline silicon on the tip of the silicon tetrachloride gas feed nozzle and grow the crude crystalline silicon downward from the tip of the silicon tetrachloride gas feed nozzle, discharging the grown crude crystalline silicon from the reactor, and treating the discharged crude crystalline silicon with an acid.

IPC Classes  ?

  • C01B 33/033 - Preparation by decomposition or reduction of gaseous or vaporised silicon compounds other than silica or silica-containing material by reduction of silicon halides or halosilanes with a metal or a metallic alloy as the only reducing agents
  • C30B 29/06 - Silicon

7.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009064702
Publication Number 2010/029843
Status In Force
Filing Date 2009-08-24
Publication Date 2010-03-18
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Saito Masayuki
  • Hattori Norikatsu

Abstract

Disclosed is a liquid crystal composition which satisfies at least one of such characteristics as high upper limit temperature of the nematic phase, low lower limit temperature of the nematic phase, low viscosity, adequate optical anisotropy, large negative dielectric anisotropy, high resistivity, high stability against ultraviolet light and high stability against heat, or has an adequate balance between at least two of the above-mentioned characteristics.  Also disclosed is an AM element having a short response time, high voltage holding ratio, high contrast ratio, long life and the like. The liquid crystal composition contains a specific compound having tetrahydropyran-2,5-diyl as a first component, and a specific compound having a large negative dielectric anisotropy as a second component, and has a negative dielectric anisotropy.  A liquid crystal display element contains the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

8.

TEMPERATURE-RESPONSIVE MAGNETIC FINE GRAINS CAPABLE OF FREEZE DRYING

      
Application Number JP2009065439
Publication Number 2010/027029
Status In Force
Filing Date 2009-09-03
Publication Date 2010-03-11
Owner CHISSO CORPORATION (Japan)
Inventor Eguchi, Masaru

Abstract

Disclosed are magnetic fine grains comprising a composite of iron oxide and polyalkylenimine, wherein the magnetic fine grains are prepared by modifying the surfaces of the magnetic fine grains with temperature-responsive macromolecules.

IPC Classes  ?

  • H01F 1/36 - Magnets or magnetic bodies characterised by the magnetic materials thereforSelection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites in the form of particles
  • C01G 49/08 - Ferroso-ferric oxide [Fe3O4]
  • C07K 16/00 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies
  • C08J 3/12 - Powdering or granulating

9.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009064528
Publication Number 2010/024164
Status In Force
Filing Date 2009-08-19
Publication Date 2010-03-04
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Hattori Norikatsu
  • Shimada Teru
  • Fujita Hiroaki
  • Kawasaki Subaru

Abstract

Disclosed is a liquid crystal composition that can satisfy at least one of properties such as a high upper limit temperature of a nematic phase, a low lower limit temperature of a nematic phase, a low viscosity, a proper optical anisotropy, a negatively high permittivity anisotropy, a high specific resistance, a high stability against ultraviolet light, and a high stability against heat, or has a proper balance between at least two of the above properties.  Also disclosed is a liquid crystal display element such as an AM element having a short response time, a high voltage retention, a high contrast ratio, and a prolonged service life. The liquid crystal composition comprises a first component of a dicyclic compound which has a negatively high permittivity anisotropy and contains fluorine at at least three of lateral positions, a second component of a specific compound having a low viscosity, and a third component of a specific compound having a negatively high permittivity anisotropy and contains a negative permittivity anisotropy.  The liquid crystal display element comprises the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

10.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009064383
Publication Number 2010/024142
Status In Force
Filing Date 2009-08-17
Publication Date 2010-03-04
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Saito Masayuki
  • Hamano Makoto

Abstract

Disclosed is a liquid crystal composition that can satisfy at least one of properties such as a high upper limit temperature of a nematic phase, a low lower limit temperature of a nematic phase, a low viscosity, a high optical anisotropy, a high permittivity anisotropy, a high specific resistance, a high stability against ultraviolet light, and a high stability against heat, or has a proper balance between at least two of the above properties.  Also disclosed is a liquid crystal display element such as an AM element having a short response time, a high voltage retention, a high contrast ratio, and a prolonged service life. The liquid crystal composition comprises a first component of a specific tetracyclic compound that has a high upper limit temperature and contains a high optical anisotropy, a second component of a specific tetracyclic compound that has a high permittivity anisotropy and contains a nematic phase.  The liquid crystal display element comprises the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

11.

METHOD FOR THE PURIFICATION OF SILICON TETRACHLORIDE

      
Application Number JP2009064507
Publication Number 2010/021339
Status In Force
Filing Date 2009-08-19
Publication Date 2010-02-25
Owner
  • CHISSO CORPORATION (Japan)
  • JX Nippon Mining & Metals Corporation (Japan)
  • TOHO TITANIUM CO., LTD. (Japan)
Inventor
  • Hayashida, Satoshi
  • Semoto, Harumichi

Abstract

Disclosed is a method for the purification of silicon tetrachloride that solves the problems of separating and removing organic chlorosilane by distillation or adsorption. A silicon tetrachloride purification method is characterized by including (1) a step to cause a mixed gas comprising silicon tetrachloride gas and oxygen-inclusive gas to come in contact with a catalyst layer that is regulated to a temperature of 200 to 450ºC and contains at least one selected from a group consisting of activated charcoal and activated charcoal on a metal carrier, and (2) a step to cool the mixed gas and separate and recover the liquid silicon tetrachloride after the aforementioned contact.

IPC Classes  ?

12.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009063148
Publication Number 2010/016387
Status In Force
Filing Date 2009-07-23
Publication Date 2010-02-11
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Hattori Norikatsu
  • Saito Masayuki

Abstract

Disclosed is a liquid crystal composition that can satisfy at least one of properties such as a high upper limit temperature of a nematic phase, a low lower limit temperature of a nematic phase, a low viscosity, a proper optical anisotropy, a negatively high permittivity anisotropy, a high specific resistance, a high stability against ultraviolet light, and a high stability against heat, or has a proper balance between at least two of the above properties.  Also disclosed is a liquid crystal display element such as an AM element having a short response time, a high voltage retention, a high contrast ratio, and a prolonged service life. The liquid crystal composition comprises a first component of a compound that has a negatively high permittivity anisotropy and contains tetrahydropyran-2,5-diyl, a second component of a specific dicyclic compound having a low viscosity, a third component of a specific compound having a high upper limit temperature, and a fourth component of a specific compound having a negatively high permittivity anisotropy, and the liquid crystal composition also has a negative permittivity anisotropy.  The liquid crystal display element comprises the composition.

IPC Classes  ?

  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

13.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009063161
Publication Number 2010/016389
Status In Force
Filing Date 2009-07-23
Publication Date 2010-02-11
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Kibe Shigeru
  • Saito Masayuki

Abstract

Disclosed is a liquid crystal composition that can satisfy at least one of properties such as a high upper limit temperature of a nematic phase, a low lower limit temperature of a nematic phase, a low viscosity, a high optical anisotropy, a high permittivity anisotropy, a high specific resistance, a high stability against ultraviolet light, and a high stability against heat, or has a proper balance between at least two of the above properties.  Also disclosed is a liquid crystal display element such as an AM element having a short response time, a high voltage retention, a high contrast ratio, and a prolonged service life. The liquid crystal composition comprises a first component of a specific compound having a negatively high permittivity anisotropy, a second component of a specific compound that has a negatively high permittivity anisotropy and contains a low lower limit temperature, a third component of a specific compound having a high upper limit temperature or a low viscosity, and a fourth component of a specific compound particularly having a negatively high permittivity anisotropy and has a negative permittivity anisotropy.  The liquid crystal display element comprises the composition.

IPC Classes  ?

  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

14.

METHODS FOR PRODUCING GLYCOL FROM GLYCERIN AND 1-PROPANOL

      
Application Number JP2009063756
Publication Number 2010/016462
Status In Force
Filing Date 2009-08-03
Publication Date 2010-02-11
Owner
  • CHISSO CORPORATION (Japan)
  • NATIONAL UNIVERSITY CORPORATION CHIBA UNIVERSITY (Japan)
Inventor
  • Sato, Satoshi
  • Akiyama, Masaki
  • Mori, Keitaro
  • Inui, Kanichiro
  • Yokota, Masahiro

Abstract

Provided are a glycol production method from glycerin that is characterized by reacting glycerin under atmospheric pressure or increased pressure in the presence of hydrogen by using a copper-containing catalyst and a 1-propanol production method that includes said production method as one step.

IPC Classes  ?

  • C07C 29/60 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by elimination of hydroxy groups, e.g. by dehydration
  • C07C 31/20 - Dihydroxylic alcohols
  • C07B 61/00 - Other general methods

15.

PACKAGING MATERIAL

      
Application Number JP2009063290
Publication Number 2010/013656
Status In Force
Filing Date 2009-07-24
Publication Date 2010-02-04
Owner CHISSO CORPORATION (Japan)
Inventor
  • Takebayashi, takafumi
  • Satou, hiroshi
  • Sanada, yoshika

Abstract

Provided is a packaging material to be used for producing and/or storing a sheet-type product for cosmetic or medical use having a desired dimension and shape and being in the form of a sponge, gel or film, which can be appropriately handled in, for example, transporting, taking out from a container or applying to the skin. A packaging material to be used for producing and/or storing a sheet-type product for cosmetic or medical use having a desired dimension and shape and being in the form of a sponge, gel or film, which comprises: a container (A) for producing/storing the sheet-type product; an inner lid (B) which is in contact with the sheet-type product in the container (A) to thereby block the movement thereof and provided with a handle for taking out from the container (A) together with the sheet-type product; and a covering material (C) which blocks the movement of the inner lid (B) and seals an opening of the container (A).

IPC Classes  ?

  • B65D 25/10 - Devices to locate articles in containers
  • A61J 1/00 - Containers specially adapted for medical or pharmaceutical purposes
  • A61K 8/02 - Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K 8/65 - CollagenGelatinKeratinDerivatives or degradation products thereof
  • A61K 9/19 - Particulate form, e.g. powders lyophilised
  • A61K 47/42 - ProteinsPolypeptidesDegradation products thereofDerivatives thereof, e.g. albumin, gelatin or zein
  • A61L 15/64 - Use of materials characterised by their function or physical properties specially adapted to be resorbable inside the body
  • B65D 1/26 - Thin-walled containers, e.g. formed by deep-drawing operations
  • B65D 25/02 - Internal fittings
  • B65D 65/40 - Applications of laminates for particular packaging purposes
  • B65D 77/20 - Container closures formed after filling by applying separate lids or covers

16.

LIQUID CRYSTALLINE COMPOUND HAVING NEGATIVE DIELECTRIC ANISOTROPY, LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009060672
Publication Number 2009/157313
Status In Force
Filing Date 2009-06-11
Publication Date 2009-12-30
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor Masukawa Tokifumi

Abstract

Disclosed is a liquid crystalline compound having excellent properties including highly negative dielectric anisotropy.  Also disclosed is a liquid crystal composition which comprises the compound.  Further disclosed is a liquid crystal display element.  Specifically disclosed is a compound having the following three factors 1) to 3): 1) a tetrahydropyran ring; 2) a terminal alkenyl chain; and 3) a group represented by formula (3).  The compound particularly has such an excellent property that the value of the dielectric anisotropy (Δε) of the compound is a higher negative number.  By using the compound having this property, it becomes possible to provide an excellent liquid crystal composition and an excellent liquid crystal display element.

IPC Classes  ?

  • C07D 309/06 - Radicals substituted by oxygen atoms
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C09K 19/54 - Additives having no specific mesophase
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

17.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009060140
Publication Number 2009/154080
Status In Force
Filing Date 2009-06-03
Publication Date 2009-12-23
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Daigo Makoto
  • Fujita Hiroaki

Abstract

Disclosed is a liquid crystal composition that satisfies at least one property of a high upper limit temperature of a nematic phase, a low lower limit temperature of a nematic phase, a low viscosity, a proper optical anisotropy, a negatively large permittivity anisotropy, a large specific resistance, a high stability against ultraviolet light, a high stability against heat and the like, or has a proper balance between at least two of the above properties.  Also disclosed is an AM element possessing a short response time, a large voltage retention, a large contrast ratio, and a long service life and the like. The liquid crystal composition that comprises a specific fluorine substituted tetracyclic compound having a high upper limit temperature as a first component and a specific compound having a negatively large permittivity anisotropy as a second component and has a negative permittivity anisotropy.  Further disclosed is a liquid crystal display element comprising the composition.

IPC Classes  ?

  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

18.

PENTACYCLIC LIQUID CRYSTAL COMPOUND HAVING CYCLOHEXANE RING, LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009060057
Publication Number 2009/150963
Status In Force
Filing Date 2009-06-02
Publication Date 2009-12-17
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor Tanaka Hiroyuki

Abstract

Disclosed is a liquid crystal compound having general physical properties necessary for a compound, stability against heat, light or the like, a wide temperature range of a liquid crystal phase, a high clearing point, good compatibility with other liquid crystal compounds, adequate optical anisotropy, and adequate dielectric anisotropy.  A liquid crystal composition containing the compound, and a liquid crystal display element containing the composition are also disclosed. Specifically disclosed are a compound represented by formula (1), a liquid crystal composition containing the compound, and a liquid crystal display element containing the composition. In formula (1), for example, R1 represents an alkyl having 1-20 carbon atoms; ring A1, ring A2, ring A3, ring A4, ring A5 and ring A6 each represents 1,4-cyclohexylene or 1,4-phenylene; Z1, Z2, Z3, Z4, Z5 and Z6 each represents a single bond; X1 represents a hydrogen or a halogen; l, m, n, o, p and q each represents 0 or 1; and l + m + n + o + p + q = 3.

IPC Classes  ?

  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C07D 319/06 - 1,3-DioxanesHydrogenated 1,3-dioxanes not condensed with other rings
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/16 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon double bonds, e.g. stilbenes
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

19.

TETRACYCLIC LIQUID CRYSTALLINE COMPOUND HAVING LATERAL FLUORINE, LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009060082
Publication Number 2009/150966
Status In Force
Filing Date 2009-06-02
Publication Date 2009-12-17
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor Kobayashi Masahide

Abstract

Disclosed is a liquid crystalline compound which is stable against heat, light or the like and has a nematic phase in a wide temperature range, while having a low viscosity, a large optical anisotropy, an adequate elastic constant K33, an adequate negative dielectric anisotropy and excellent compatibility with other liquid crystalline compounds.  A liquid crystal composition containing the liquid crystalline compound, and a liquid crystal display element containing the liquid crystal composition are also disclosed. The liquid crystalline compound is represented by formula (a). In formula (a), R1 and R2 each represents an alkyl having 1-10 carbon atoms, an alkenyl having 2-10 carbon atoms or an alkoxy having 1-9 carbon atoms; ring A1 and ring A2 each represents 1,4-phenylene or trans-1,4-cyclohexylene; L1 and L2 each represents a hydrogen or a fluorine, and at least one of L1 and L2 is a fluorine; and Z1 and Z2 each represents a single bond, -(CH2)2-, -CH=CH-, -CH2O- or -OCH2-.

IPC Classes  ?

  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C07C 25/18 - Polycyclic aromatic halogenated hydrocarbons
  • C07C 43/184 - Ethers having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring to a carbon atom of a non-condensed ring
  • C07C 43/21 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing rings other than six-membered aromatic rings
  • C07C 69/757 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring having any of the groups OH, O-metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
  • C07C 69/94 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring of polycyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of six-membered aromatic rings
  • C07D 319/06 - 1,3-DioxanesHydrogenated 1,3-dioxanes not condensed with other rings
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/16 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon double bonds, e.g. stilbenes
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

20.

LIQUID CRYSTALLINE TETRACYCLIC COMPOUND HAVING FLUORINE ATOM, LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009059319
Publication Number 2009/145101
Status In Force
Filing Date 2009-05-21
Publication Date 2009-12-03
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Kubo takahiro
  • Shimada teru

Abstract

Disclosed is a liquid crystalline compound which is stable against heat, light or the like and has a nematic phase in a wide temperature range, while having a low viscosity, an adequate optical anisotropy, an adequate dielectric anisotropy and excellent compatibility with other liquid crystalline compounds.  A liquid crystal composition containing the liquid crystalline compound, and a liquid crystal display element containing the liquid crystal composition are also disclosed. The liquid crystalline compound is represented by formula (a). In formula (a), Ra represents, for example, an alkyl having 1-10 carbon atoms; Rb represents, for example, an alkenyl having 2-10 carbon atoms; La represents, for example, a hydrogen; and Z1, Z2 and Z3 each represents, for example, a single bond.  The liquid crystal composition contains the liquid crystalline compound, and the liquid crystal display element contains the liquid crystal composition.

IPC Classes  ?

  • C07C 25/24 - Halogenated aromatic hydrocarbons with unsaturated side chains
  • C07C 25/18 - Polycyclic aromatic halogenated hydrocarbons
  • C07C 43/192 - Ethers having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring containing halogen
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/16 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon double bonds, e.g. stilbenes
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C09K 19/54 - Additives having no specific mesophase
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

21.

OPTICALLY ISOTROPIC LIQUID CRYSTALLINE MEDIUM, AND OPTICAL ELEMENT

      
Application Number JP2009058680
Publication Number 2009/139330
Status In Force
Filing Date 2009-05-08
Publication Date 2009-11-19
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Haseba yasuhiro
  • Sago kohki
  • Kuninobu takafumi

Abstract

Disclosed is a liquid crystalline medium which has a wide liquid crystal phase temperature range, a high refractive index anisotropy and high dielectric anisotropy, and has an optically isotropic liquid crystal phase. The liquid crystalline medium comprises a liquid crystalline compound having a pyridine ring and a linking group –CF2O- and a chiral agent, and can exhibit an optically isotropic liquid crystal phase.

IPC Classes  ?

  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C07D 239/26 - Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
  • C07D 493/04 - Ortho-condensed systems
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/16 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon double bonds, e.g. stilbenes
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/54 - Additives having no specific mesophase
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
  • G02F 1/137 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering

22.

LIQUID CRYSTALLINE COMPOUND WITH NEGATIVE DIELECTRIC ANISOTROPY, LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY DEVICE

      
Application Number JP2009057585
Publication Number 2009/136534
Status In Force
Filing Date 2009-04-15
Publication Date 2009-11-12
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor Masukawa, Tokifumi

Abstract

Disclosed is a liquid crystalline compound having excellent characteristics such as large negative dielectric anisotropy. A liquid crystal composition using the compound and a liquid crystal display device are also disclosed. A compound containing 1) a tetrahydropyran ring, 2) -CH2O- or -OCH2-, and 3) a group represented by formula (A) exhibits such an excellent characteristic that the value of dielectric anisotropy increases in the negative direction. By using a compound having such a characteristic, there can be obtained an excellent liquid crystal composition and an excellent liquid crystal display device.

IPC Classes  ?

  • C07D 309/06 - Radicals substituted by oxygen atoms
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/16 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon double bonds, e.g. stilbenes
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C09K 19/54 - Additives having no specific mesophase
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

23.

TRICYCLIC LIQUID CRYSTALLINE COMPOUND HAVING LATERAL FLUORINE, LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY DEVICE

      
Application Number JP2009055920
Publication Number 2009/125668
Status In Force
Filing Date 2009-03-25
Publication Date 2009-10-15
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor Kobayashi, Masahide

Abstract

Provided are a liquid crystal compound represented by the general formula (I) which is stable against heat, light, etc., shows a nematic phase in a wide temperature range, has a low viscosity, a high optical anisotropy and an appropriate elastic constant K33 (K33: bend elastic constant), and further has suitable negative dielectric anisotropy and excellent compatibility with another liquid crystalline compound; and a liquid crystal composition containing the compound. In the formula, R1 and R2 are hydrogen, alkyl or the like; the ring A1 is trans-1,4-cyclohexylene, 1,4-phenylene or the like; L1 to L4 are hydrogen or fluorine, with the proviso that at least three of them are fluorine; when the ring A1 is trans-1,4-cyclohexylene or the like, Z1 is a single bond, -(CH2)2- or the like; when the ring A1 is 1,4-phenylene, Z1 is -(CH2)2- or the like.

IPC Classes  ?

  • C07C 43/23 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
  • C07C 43/21 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing rings other than six-membered aromatic rings
  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/16 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon double bonds, e.g. stilbenes
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
  • G02F 1/139 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering based on orientation effects in which the liquid crystal remains transparent

24.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2009055921
Publication Number 2009/125669
Status In Force
Filing Date 2009-03-25
Publication Date 2009-10-15
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor Saito, Masayuki

Abstract

Disclosed is a liquid crystal composition that can satisfy at least one of properties such as a high upper limit temperature of a nematic phase, a low lower limit temperature of the nematic phase, a low viscosity, a high optical anisotropy, a high permittivity anisotropy, a high specific resistance, a high stability against ultraviolet light, and a high heat stability, or has a proper balance of at least two of the above properties. Also disclosed is an AM element having a short response time, a high voltage retention, a high contrast ratio, a prolonged service life and the like. The liquid crystal composition comprises a first component of a specific compound having a high permittivity anisotropy, particularly a high negative permittivity anisotropy, a second component of a specific compound having a high negative permittivity anisotropy, and a low lower limit temperature, and a third component of a specific compound having a high upper limit temperature or a low viscosity and has a negative permittivity anisotropy. Also disclosed is a liquid crystal display element comprising the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
  • G02F 1/139 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering based on orientation effects in which the liquid crystal remains transparent

25.

DETECTION METHOD AND DETERMINATION METHOD FOR DETECTION TARGET

      
Application Number JP2008073626
Publication Number 2009/084596
Status In Force
Filing Date 2008-12-25
Publication Date 2009-07-09
Owner
  • Ortho-Clinical Diagnostics Kabushiki Kaisha (Japan)
  • CHISSO CORPORATION (Japan)
Inventor
  • Sawai, Toshiya
  • Oowada, Eri
  • Nagaoka, Hirokazu
  • Sugita, Satoru
  • Ueki, Toshiya

Abstract

It is intended to provide a detection method and a determination method for detection target capable of detecting and determining a detection target promptly and simply with high accuracy at low cost. The detection method includes the steps of: mixing a first conjugate 10 in which a first substance containing a stimulus-responsive polymer 11 and a particulate magnetic substance 19 is conjugated to a first antibody 13 against a detection target 50 with a sample; applying a magnetic force after placing the resulting mixture in a condition capable of aggregating the stimulus-responsive polymer 11; measuring a generated magnetic field; and detecting the detection target 50 based on the degree of increase in the magnetic field after applying the magnetic force.

IPC Classes  ?

  • G01N 33/543 - ImmunoassayBiospecific binding assayMaterials therefor with an insoluble carrier for immobilising immunochemicals

26.

METHOD OF DETECTING SUBSTANCE TO BE DETECTED AND METHOD OF DETERMINATION

      
Application Number JP2008073625
Publication Number 2009/084595
Status In Force
Filing Date 2008-12-25
Publication Date 2009-07-09
Owner
  • Ortho-Clinical Diagnostics Kabushiki Kaisha (Japan)
  • CHISSO CORPORATION (Japan)
Inventor
  • Sawai, Toshiya
  • Oowada, Eri
  • Sato, Yasunobu
  • Nagaoka, Hirokazu
  • Sugita, Satoru

Abstract

A detection/determination kit with which a substance to be detected or the amount thereof can be rapidly, inexpensively, and easily detected or determined; and a detection/determination method. The kit, which is for detecting a substance to be detected (50) contained in a specimen, comprises: a first compound (10) comprising a first substance including a stimulus-responsive polymer (11) and, bonded to the first substance, a first antibody (13) against the substance (50); and a second compound (20) comprising a second substance (21) which is hydrophilic and, bonded thereto, a second antibody (23) against the substance (50). The first antibody (13) and second antibody (23) can simultaneously combine with the substance (50) at different sites in the substance (50).

IPC Classes  ?

  • G01N 33/531 - Production of immunochemical test materials
  • G01N 33/543 - ImmunoassayBiospecific binding assayMaterials therefor with an insoluble carrier for immobilising immunochemicals

27.

LIQUID CRYSTALLINE COMPOUND, LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008065665
Publication Number 2009/034867
Status In Force
Filing Date 2008-09-01
Publication Date 2009-03-19
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Shimada, Teru
  • Kobayashi, Masahide

Abstract

Disclosed is a liquid crystalline compound which is stable to heat, light and the like, exhibits a nematic phase in a wide temperature range, has a low viscosity, adequate optical anisotropy, an adequate elastic coefficient K33 and adequate negative dielectric anisotropy, and also has excellent compatibility with other liquid crystalline compound. Also disclosed is a liquid crystal composition comprising the compound, which is stable to heat, light and the like, has a low viscosity, adequate optical anisotropy, adequate negative dielectric anisotropy and an adequate elastic coefficient K33, has a low threshold voltage, and exhibits a nematic phase having a high upper-limit temperature and a low lower-limit temperature. Further disclosed is a liquid crystal display element comprising the composition, which has a short response time, a small power consumption, a low driving voltage and a large contrast, and can be used in a wide temperature range. Specifically disclosed are: a liquid crystalline compound having four or more rings, wherein the central ring has a 2,3-difluorophenoxy, such as trans-4'-[2,3-difluoro-4- (trans-4-propylcyclohexyl)phenoxymethyl]-trans-4-pentyl- bicyclohexyl; a liquid crystal composition comprising the compound; and a liquid crystal display element utilizing the liquid crystal composition.

IPC Classes  ?

  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C07C 69/75 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of acids with a six-membered ring
  • C07C 69/773 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring esterified with a hydroxy compound having the esterified hydroxy group bound to a carbon atom of a six-membered aromatic ring
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/137 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering

28.

TETRA- OR PENTA-CYCLIC LIQUID CRYSTALLINE COMPOUND HAVING LATERAL FLUORINE, LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008065187
Publication Number 2009/031437
Status In Force
Filing Date 2008-08-26
Publication Date 2009-03-12
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Kobayashi, Masahide
  • Shimada, Teru

Abstract

Disclosed is a liquid crystalline compound which has stability to heat, light and the like, exhibits a nematic phase in a wide temperature range, has a low viscosity, adequate optical anisotropy and an adequate elastic coefficient K33, and also has adequate negative dielectric anisotropy and excellent compatibility with other liquid crystalline compound. Also disclosed is a liquid crystal composition comprising the compound, which has stability to heat, light and the like, has a low viscosity, large optical anisotropy, adequate negative dielectric anisotropy and an adequate elastic coefficient K33, also has a low threshold voltage, and exhibits a nematic phase having a high upper-limit temperature (i.e., a nematic-to-isotropic phase transition temperature) and a low lower-limit temperature. Specifically disclosed is a liquid crystalline compound which has a fluorine in the lateral position, and which has a specific structure having a phenylene in which a hydrogen on the benzene ring is substituted by a fluorine. Also specifically disclosed is a liquid crystal composition comprising the compound.

IPC Classes  ?

  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C07D 309/06 - Radicals substituted by oxygen atoms
  • C07D 319/06 - 1,3-DioxanesHydrogenated 1,3-dioxanes not condensed with other rings
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
  • G02F 1/139 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering based on orientation effects in which the liquid crystal remains transparent

29.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008065083
Publication Number 2009/028443
Status In Force
Filing Date 2008-08-25
Publication Date 2009-03-05
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Kibe, Shigeru
  • Saito, Masayuki

Abstract

Disclosed are: a liquid crystal composition which satisfies at least one property selected from a high upper limit temperature in a nematic phase, a low lower limit temperature in a nematic phase, a low viscosity, high optical anisotropy, high dielectric anisotropy, a high specific resistance, high stability against ultraviolet ray, high stability against heat and the like or has a proper balance between at least two properties selected from the above-mentioned properties; and an AM element having a short response time, a high voltage holding ratio, a high contrast ratio, a long service life and the like. Specifically disclosed are: a liquid crystal composition which comprises a specific pentacyclic compound having high optical anisotropy and high dielectric anisotropy as the first component, a specific compound having a low viscosity as the second component, and a specific tetracyclic compound having a high upper limit temperature as the third component, and which shows a nematic phase; and a liquid crystal display element comprising the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

30.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008065088
Publication Number 2009/028446
Status In Force
Filing Date 2008-08-25
Publication Date 2009-03-05
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Kibe, Shigeru
  • Saito, Masayuki

Abstract

Disclosed are: a liquid crystal composition which satisfies at least one property selected from a high upper limit temperature in a nematic phase, a low lower limit temperature in a nematic phase, a low viscosity, high optical anisotropy, high dielectric anisotropy, a high specific resistance, high stability against ultraviolet ray, high stability against heat and the like or has a proper balance between at least two properties selected from the above-mentioned properties; and an AM element having a short response time, a high voltage holding ratio, a high contrast ratio, a long service life and the like. Specifically disclosed are: a liquid crystal composition which comprises a specific pentacyclic compound having high optical anisotropy and high dielectric anisotropy as the first component and a specific compound having a low viscosity as the second component, and which shows a nematic phase; and a liquid crystal display element comprising the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

31.

LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008064804
Publication Number 2009/028367
Status In Force
Filing Date 2008-08-20
Publication Date 2009-03-05
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Saito, Masayuki
  • Kibe, Shigeru

Abstract

Disclosed are: a liquid crystal composition, which satisfies at least one property selected from a high upper-limit temperature in a nematic phase, a low lower-limit temperature in a nematic phase, a low viscosity, high optical anisotropy, high dielectric anisotropy, a high specific resistivity, high stability to ultraviolet ray, high stability to heat and the like, or which has an adequate balance between at least two properties selected from the above-mentioned properties; and an AM element having a short response time, a high voltage holding ratio, a high contrast ratio, a long service life and the like. Specifically disclosed are: a liquid crystal composition which comprises a specific pentacyclic compound having high optical anisotropy and high dielectric anisotropy as the first component and a specific compound having a low viscosity as the second component and which has a nematic phase; and a liquid crystal display element comprising the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

32.

LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008064805
Publication Number 2009/028368
Status In Force
Filing Date 2008-08-20
Publication Date 2009-03-05
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Saito, Masayuki
  • Kibe, Shigeru

Abstract

Disclosed are: a liquid crystal composition, which satisfies at least one property selected from a high upper-limit temperature in a nematic phase, a low lower-limit temperature in a nematic phase, a low viscosity, high optical anisotropy, high dielectric anisotropy, a high specific resistivity, high stability to ultraviolet ray, high stability to heat and the like, or which has an adequate balance between at least two properties selected from the above-mentioned properties; and an AM element having a short response time, a high voltage holding ratio, a high contrast ratio, a long service life and the like. Specifically disclosed are: a liquid crystal composition which comprises a specific pentacyclic compound having high optical anisotropy and high dielectric anisotropy as the first component, a specific compound having a low viscosity as the second component, and a specific tetracyclic compound having a high upper-limit temperature as the third component, and which has a nematic phase; and a liquid crystal display element comprising the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

33.

POLYMERIZABLE LIQUID CRYSTALLINE COMPOUND, LIQUID CRYSTAL COMPOSITION, AND POLYMER

      
Application Number JP2008057420
Publication Number 2008/136265
Status In Force
Filing Date 2008-04-16
Publication Date 2008-11-13
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Inagaki, Junichi
  • Yano, Tomohiro
  • Ootsuki, Daisuke
  • Ito, Maiko
  • Shundo, Ryushi

Abstract

Disclosed is a compound represented by the formula (1) below. In the formula (1) below, R1 and R2 each represents a hydrogen, a fluorine, a chlorine, a methyl or an ethyl; X1 and X 2 each represents a hydrogen, a fluorine, a methyl or a trifluoromethyl; Z1 and Z2 each represents a single bond, -COO-, -OCO-, -CH=CH-COO-, -OCO-CH=CH-, -CH2CH2-COO-, -OCO-CH2CH2-, -CH2O-, -CONH-, -(CH2)4-, -CH2CH2- or -C≡C-; Z3 and Z4 each represents a single bond or -O-; A1 and A2 each represents 1,4-cyclohexylene, 1,4-phenylene, 1,3-phenylene, pyridine-2,5-diyl, pyrimidine-2,5-diyl, naphthalene-2,6-diyl or tetrahydronaphthalene-2,6-diyl; and Y1 and Y2 each represents an alkylene having 2-20 carbon atoms.

IPC Classes  ?

  • C07C 69/78 - Benzoic acid esters
  • C07C 69/96 - Esters of carbonic or haloformic acids
  • C08F 20/10 - Esters
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/38 - Polymers, e.g. polyamides
  • G02B 5/30 - Polarising elements
  • G02F 1/1335 - Structural association of cells with optical devices, e.g. polarisers or reflectors
  • G02F 1/13363 - Birefringent elements, e.g. for optical compensation

34.

POLYAMINO ACID SYNTHETASE AND GENE ENCODING THE SAME

      
Application Number JP2008057618
Publication Number 2008/130034
Status In Force
Filing Date 2008-04-18
Publication Date 2008-10-30
Owner CHISSO CORPORATION (Japan)
Inventor
  • Yamanaka, Kazuya
  • Hamano, Yoshimitu

Abstract

It is intended to provide an enzyme which catalyzes amino acid polymerization in the nonribosomal peptide synthetase (NRPS) type and a gene encoding the same.

IPC Classes  ?

  • C12N 15/09 - Recombinant DNA-technology
  • C07K 16/40 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against enzymes
  • C12N 1/15 - Fungi Culture media therefor modified by introduction of foreign genetic material
  • C12N 1/19 - YeastsCulture media therefor modified by introduction of foreign genetic material
  • C12N 1/21 - BacteriaCulture media therefor modified by introduction of foreign genetic material
  • C12N 5/10 - Cells modified by introduction of foreign genetic material, e.g. virus-transformed cells
  • C12N 9/00 - Enzymes, e.g. ligases (6.)ProenzymesCompositions thereofProcesses for preparing, activating, inhibiting, separating, or purifying enzymes
  • C12P 13/00 - Preparation of nitrogen-containing organic compounds
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • G01N 33/15 - Medicinal preparations
  • G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing

35.

POLYMER AND SURFACE-TREATING AGENT CONTAINING THE POLYMER

      
Application Number JP2008055218
Publication Number 2008/123122
Status In Force
Filing Date 2008-03-21
Publication Date 2008-10-16
Owner CHISSO CORPORATION (Japan)
Inventor
  • Ito, Kenya
  • Oikawa, Hisao
  • Ohguma, Koji
  • Yamahiro, Mikio

Abstract

It is intended to provide a polymer which is excellent in, for example, water and oil repellency, antifouling property and charge control property. It is also intended to provide a (surface) treating agent which is excellent in, for example, water and oil repellency, antifouling property and charge control property. The above problems are solved by providing a polymer, which comprises a structural unit derived from fluorosil sesqui oxane having an addition-polymerizable functional group, or a structural unit derived from fluorosil sesqui oxane having an addition-polymerizable functional group together with a structural unit derived from organopolysiloxane having an addition-polymerizable functional group; a surface-treating agent containing the above-described polymer; a material having been treated with the above-described agent; and so on.

IPC Classes  ?

  • C08F 230/08 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
  • C08F 290/06 - Polymers provided for in subclass
  • C09D 143/04 - Homopolymers or copolymers of monomers containing silicon
  • C09K 3/18 - Materials not provided for elsewhere for application to surface to minimize adherence of ice, mist or water theretoThawing or antifreeze materials for application to surfaces

36.

INK-JET INK

      
Application Number JP2008055420
Publication Number 2008/123190
Status In Force
Filing Date 2008-03-24
Publication Date 2008-10-16
Owner CHISSO CORPORATION (Japan)
Inventor
  • Hanafusa, Shinsuke
  • Hattori, Takayuki
  • Eguchi, Kaori
  • Furuta, Tomotsugu
  • Shimizu, Tomoaki

Abstract

[PROBLEMS] To provide an ink-jet ink which can form a polyimide film having a relatively large thickness (1 &mgr;m or more) by a single of jetting. [MEANS FOR SOLVING PROBLEMS] Disclosed is an ink-jet ink comprising at least one member selected from a silicon compound (A) produced from a compound (a1) having two or more acid anhydride groups and a monoamine (a2) and a silicon compound (A') produced from a compound (a1') having one acid anhydride group and a diamine (a2').

IPC Classes  ?

37.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008054908
Publication Number 2008/114779
Status In Force
Filing Date 2008-03-17
Publication Date 2008-09-25
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Kibe, Shigeru
  • Hattori, Norikatsu
  • Saito, Masayuki

Abstract

Disclosed are: a liquid crystal composition which satisfies at least one property selected from a high upper temperature limit of a nematic phase thereof, a low lower temperature limit of a nematic phase thereof, a low viscosity, high optical anisotropy, high negative dielectric anisotropy, a high specific resistivity, high stability against ultraviolet ray, high stability against heat and the like, or which has a proper balance between at least two properties selected from the above-mentioned properties; and an AM element having a short response time, a high voltage holding ratio, a high contrast ratio, a long service life and the like. Specifically disclosed are: a liquid crystal composition which comprises a specific compound having high negative optical anisotropy as a first component and a specific bicyclic compound having a particularly low viscosity as a second component, and which exhibits a nematic phase; and a liquid crystal display element comprising the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

38.

LIQUID-CRYSTAL COMPOSITION AND LIQUID-CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008055097
Publication Number 2008/114821
Status In Force
Filing Date 2008-03-19
Publication Date 2008-09-25
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Hattori, Norikatsu
  • Kibe, Shigeru
  • Saito, Masayuki

Abstract

A liquid-crystal composition which satisfies at least one of the following properties or has an adequate balance between at least two of the following properties: a high upper-limit temperature for nematic phase, low lower-limit temperature for nematic phase, low viscosity, high optical anisotropy, high negative permittivity anisotropy, high resistivity, high stability to ultraviolet, high stability to heat, and the like. The liquid-crystal composition comprises at least one compound selected from the group consisting of compounds represented by the formulae (1-1) and (1-2) and at least one compound selected from the group consisting of compounds represented by the formulae (2-1) and (2-2). For example, R1 and R2 each is C1-12 alkyl; Z1 is a single bond; and one of rings A and B is tetrahydropyran-2,5-diyl and the other is 1,4-cyclohexylene or 1,4-phenylene.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

39.

PENTACYCLIC LIQUID CRYSTAL COMPOUND HAVING CF2O BONDING GROUP, LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY

      
Application Number JP2008052820
Publication Number 2008/105286
Status In Force
Filing Date 2008-02-20
Publication Date 2008-09-04
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor Tanaka, Hiroyuki

Abstract

Disclosed is a novel compound, namely a pentacyclic liquid crystal compound having a CF2O bonding group, which has general physical properties necessary for a compound, stability against heat and light, a wide temperature range of a liquid crystal phase, a high clearing point, good compatibility with other compounds, and large dielectric anisotropy and large refractive anisotropy. This pentacyclic liquid crystal compound has a particularly high clearing point and particularly large refractive anisotropy. Also disclosed are a liquid crystal composition and a liquid crystal display.

IPC Classes  ?

  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C07D 319/06 - 1,3-DioxanesHydrogenated 1,3-dioxanes not condensed with other rings
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups

40.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008051855
Publication Number 2008/102641
Status In Force
Filing Date 2008-02-05
Publication Date 2008-08-28
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Saito, Masayuki
  • Goto, Shuichi

Abstract

Disclosed are: a liquid crystal composition which satisfies at least one property selected from a high upper temperature limit of a nematic phase thereof, a low lower temperature limit of a nematic phase thereof, a low viscosity, high optical anisotropy, high dielectric anisotropy, a high specific resistivity, high stability against ultraviolet ray, high stability against heat and the like, or which has a proper balance between at least two properties selected from the above-mentioned properties; and an AM element having a short response time, a high voltage holding ratio, a high contrast ratio, a long service life and the like. Specifically disclosed are: a liquid crystal composition which comprises a specific tricyclic compound having high optical anisotropy as a first component, a specific tetracyclic compound having high dielectric anisotropy as a second component and a specific bicyclic compound having a particularly low viscosity as a third component, and which exhibits a nematic phase; and a liquid crystal display element comprising the composition.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

41.

LIQUID CRYSTALLINE COMPOUND, LIQUID CRYSTAL COMPOSITION, LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2008050353
Publication Number 2008/090780
Status In Force
Filing Date 2008-01-15
Publication Date 2008-07-31
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor Shimada, Teru

Abstract

Disclosed are: a liquid crystalline compound which is stable to heat, light and the like, exhibits a liquid crystal phase in a wide temperature range, has a small viscosity, adequate optical anisotropy, large dielectric anisotropy, and excellent compatibility with other liquid crystalline compound; a liquid crystal composition having adequate optical anisotropy and dielectric anisotropy and a low threshold voltage, and exhibits a nematic phase having a high upper-limit temperature and a low lower-limit temperature; and a liquid crystal display element having a short response time, a small power consumption, a small driving voltage and a large contrast, and can be used in a wide temperature range. For example, a halogenobenzene derivative having a trifluoropropenyl group or a trifluoropropynyl group in a side chain, such as trans-4'-[3,5-difluoro-4-(3,3,3-trifluoropropenyl)phenyl]- trans-4-propylbicyclohexyl, can be used as the liquid crystalline compound. The liquid crystal composition comprises the derivative. The liquid crystal display element utilizes the liquid crystal composition.

IPC Classes  ?

  • C07C 25/24 - Halogenated aromatic hydrocarbons with unsaturated side chains
  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C07C 69/773 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a six-membered aromatic ring esterified with a hydroxy compound having the esterified hydroxy group bound to a carbon atom of a six-membered aromatic ring
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/16 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon double bonds, e.g. stilbenes
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

42.

METAL SALT OF CROSSLINKED CELLULOSE DERIVATIVE

      
Application Number JP2007075028
Publication Number 2008/078795
Status In Force
Filing Date 2007-12-26
Publication Date 2008-07-03
Owner CHISSO CORPORATION (Japan)
Inventor
  • Yoshida, Naoyuki
  • Ishida, Kazushi
  • Sasaki, Shuji
  • Yamaoka, Ippei

Abstract

Disclosed is a metal salt of a crosslinked cellulose derivative represented by the general formula (I) below, wherein the substitution degree of hydroxy groups in the glucose units of the crosslinked cellulose derivative by a functional group a is not less than 1. R-O-A (I) (In the formula (I), R represents a crosslinked cellulose residue, and A represents a functional group a having cation-exchange ability.)

IPC Classes  ?

  • C08B 5/14 - Cellulose sulfate
  • A61K 31/717 - Celluloses
  • A61P 3/12 - Drugs for disorders of the metabolism for electrolyte homeostasis
  • C08B 5/00 - Preparation of cellulose esters of inorganic acids
  • C08B 11/10 - Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals substituted with acid radicals
  • C08B 11/12 - Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals substituted with acid radicals substituted with carboxylic radicals

43.

SODIUM ABSORPTION INHIBITOR, POTASSIUM ABSORPTION INHIBITOR, PHOSPHORUS ABSORPTION INHIBITOR AND PREVENTIVE AGENT, THERAPEUTIC AGENT AND FOOD CONTAINING THE SAME

      
Application Number JP2007075030
Publication Number 2008/078797
Status In Force
Filing Date 2007-12-26
Publication Date 2008-07-03
Owner
  • OTSUKA PHARMACEUTICAL FACTORY, INC. (Japan)
  • CHISSO CORPORATION (Japan)
Inventor
  • Yamaoka, Ippei
  • Yoshida, Naoyuki
  • Ishida, Kazushi
  • Sasaki, Shuji

Abstract

A sodium absorption inhibitor, a potassium absorption inhibitor, and a phosphorus absorption inhibitor, each of which contains as an active ingredient, a metal salt of a cross-linked cellulose derivative represented by the following general formula (I), and a preventive agent, a therapeutic agent and a food for diseases caused by overconsumption of table salt, potassium and phosphorus or diseases which require restriction of intake of table salt, potassium, and phosphorus are provided. With the use of them, overconsumed table salt, potassium, and phosphorus can be actively and safely excreted outside the body. R-O-A (I) (In the formula (I), R represents a cross-linked cellulose residue, and A represents a functional group a having a cation exchange ability.)

IPC Classes  ?

  • C08B 5/14 - Cellulose sulfate
  • A61K 31/717 - Celluloses
  • A61P 3/12 - Drugs for disorders of the metabolism for electrolyte homeostasis
  • C08B 5/10 - Reducing the viscosity
  • C08B 11/10 - Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals substituted with acid radicals
  • C08B 11/12 - Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals substituted with acid radicals substituted with carboxylic radicals

44.

SUBSTANCE CAPABLE OF INDUCING PLATELET AGGREGATION

      
Application Number JP2007073910
Publication Number 2008/075589
Status In Force
Filing Date 2007-12-12
Publication Date 2008-06-26
Owner CHISSO CORPORATION (Japan)
Inventor
  • Umeda, Yasuto
  • Takasaki, Shinichi
  • Takebayashi, Takafumi
  • Kawai, Takahiro

Abstract

Disclosed is a substance capable of inducing platelet aggregation, which comprises a polypeptide having a peptide fragment (component A) represented by the formula (1) as an active ingredient. -(Pro-X-Gly)n- (1) wherein X represents Pro or Hyp; and n represents an integer of 20 to 5000.

IPC Classes  ?

  • C07K 14/78 - Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin or cold insoluble globulin [CIG]
  • G01N 33/49 - Physical analysis of biological material of liquid biological material blood

45.

FLUORINE-CONTAINING POLYMER AND RESIN COMPOSITION

      
Application Number JP2007074235
Publication Number 2008/072765
Status In Force
Filing Date 2007-12-17
Publication Date 2008-06-19
Owner CHISSO CORPORATION (Japan)
Inventor
  • Oikawa, Hisao
  • Ohguma, Koji
  • Ito, Kenya
  • Yamahiro, Mikio

Abstract

Disclosed is a polymer containing a structural unit A derived from a fluorosilsesquioxane having one addition polymerizable functional group in a molecule, a structural unit B derived from an organopolysiloxane having an addition polymerizable functional group, a structural unit C derived from an addition polymerizable monomer containing a group having an active hydrogen, and optionally a structural unit D derived from an addition polymerizable monomer other than the fluorosilsesquioxane having one addition polymerizable functional group in a molecule, the organopolysiloxane having an addition polymerizable functional group and the addition polymerizable monomer containing a group having an active hydrogen.

IPC Classes  ?

  • C08F 290/06 - Polymers provided for in subclass
  • C08L 55/00 - Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups
  • C09D 155/00 - Coating composition based on homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups

46.

FLUORINE-CONTAINING POLYMER AND RESIN COMPOSITION

      
Application Number JP2007074238
Publication Number 2008/072766
Status In Force
Filing Date 2007-12-17
Publication Date 2008-06-19
Owner CHISSO CORPORATION (Japan)
Inventor
  • Oikawa, Hisao
  • Ohguma, Koji
  • Ito, Kenya
  • Nakayama, Minoru
  • Koga, Shin
  • Yamahiro, Mikio
  • Sato, Hiroyuki

Abstract

Disclosed is a polymer containing a structural unit A derived from a fluorosilsesquioxane having one addition polymerizable functional group in a molecule, a structural unit B derived from an organopolysiloxane having an addition polymerizable functional group, a structural unit C with a group having a polymerizable unsaturated bond in a side chain, which unit is derived from an addition polymerizable monomer, and optionally a structural unit D derived from an addition polymerizable monomer other than the fluorosilsesquioxane having one addition polymerizable functional group in a molecule, the organopolysiloxane having an addition polymerizable functional group and the addition polymerizable monomer having a functional group capable of introducing a group having a polymerizable unsaturated bond.

IPC Classes  ?

  • C08F 290/06 - Polymers provided for in subclass
  • C08F 8/14 - Esterification
  • C08F 8/30 - Introducing nitrogen atoms or nitrogen-containing groups
  • C08F 290/12 - Polymers provided for in subclasses or
  • C08F 299/00 - Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
  • C09D 155/00 - Coating composition based on homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups

47.

COSMETIC COMPOSITION

      
Application Number JP2007073275
Publication Number 2008/066193
Status In Force
Filing Date 2007-11-27
Publication Date 2008-06-05
Owner CHISSO CORPORATION (Japan)
Inventor
  • Yoshida, Naoyuki
  • Yamamoto, Yuichi
  • Ishida, Kazushi
  • Yoda, Akiko
  • Sasaki, Syuji

Abstract

Disclosed is a cosmetic composition having a moisturizing effect and a high capability of inhibiting hyaluronidase activity. The cosmetic composition comprises a combination of at least one member selected from sulfated cellulose and a salt thereof and a polyhydric alcohol. The cosmetic composition enables to further improve the moisturizing effect and the capability of inhibiting hyaluronidase activity of sulfated cellulose. The cosmetic composition may further comprise an electrolyte having a pH-buffering ability to improve the stability of the cosmetic composition.

IPC Classes  ?

  • A61K 8/73 - Polysaccharides
  • A61K 8/02 - Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K 8/34 - Alcohols
  • A61Q 1/00 - Make-up preparationsBody powdersPreparations for removing make-up
  • A61Q 5/00 - Preparations for care of the hair
  • A61Q 19/00 - Preparations for care of the skin
  • A61Q 19/10 - Washing or bathing preparations

48.

INKJET INK

      
Application Number JP2007072488
Publication Number 2008/059986
Status In Force
Filing Date 2007-11-14
Publication Date 2008-05-22
Owner CHISSO CORPORATION (Japan)
Inventor
  • Tanioka, Satoshi
  • Eguchi, Kaori
  • Kikukawa, Takashi
  • Anraku, Hiroshi
  • Hanafusa, Shinsuke

Abstract

There has been required an inkjet ink which enables to form a relatively thick film by a single jet. Disclosed is an inkjet ink containing at least one alkenyl-substituted nadimide compound. Also disclosed are such an inkjet ink additionally containing a polymer compound and such an inkjet ink additionally containing a solvent.

IPC Classes  ?

  • C09D 11/00 - Inks
  • B05D 1/26 - Processes for applying liquids or other fluent materials performed by applying the liquid or other fluent material from an outlet device in contact with, or almost in contact with, the surface
  • B41M 5/00 - Duplicating or marking methodsSheet materials for use therein

49.

THROMBIN MUTANT

      
Application Number JP2007072169
Publication Number 2008/059917
Status In Force
Filing Date 2007-11-15
Publication Date 2008-05-22
Owner
  • CHISSO CORPORATION (Japan)
  • FUJIMORI KOGYO CO., LTD. (Japan)
Inventor
  • Hosokawa, Kazuya
  • Wada, Tomoko

Abstract

A thrombin mutant in which at least serine at position 205 among amino acids in the active center of the thrombin B-chain has been substituted with another amino acid, and further any one or more of the following substitutions have been introduced: (I) substitution of arginine at position 89 in the B-chain with another amino acid; (II) substitution of threonine at position 69 in the B-chain or serine at position 22 in the B-chain with another amino acid; (III) substitution of alanine at position 200 in the B-chain with another amino acid; and (IV) substitution of lysine at position 65 in the B-chain with threonine.

IPC Classes  ?

  • C12N 15/09 - Recombinant DNA-technology
  • A61K 38/55 - Protease inhibitors
  • A61P 7/02 - Antithrombotic agentsAnticoagulantsPlatelet aggregation inhibitors
  • C12N 1/15 - Fungi Culture media therefor modified by introduction of foreign genetic material
  • C12N 1/19 - YeastsCulture media therefor modified by introduction of foreign genetic material
  • C12N 1/21 - BacteriaCulture media therefor modified by introduction of foreign genetic material
  • C12N 5/10 - Cells modified by introduction of foreign genetic material, e.g. virus-transformed cells
  • C12N 9/74 - Thrombin

50.

THERMO-RESPONSIVE POLYLYSINE

      
Application Number JP2007067041
Publication Number 2008/029739
Status In Force
Filing Date 2007-08-31
Publication Date 2008-03-13
Owner
  • OSAKA UNIVERSITY (Japan)
  • CHISSO CORPORATION (Japan)
Inventor
  • Akashi, Mitsuru
  • Shimokuri, Taiki

Abstract

Disclosed is a novel stimuli-responsive polymer which has biodegradability and biocompatibility and which can develop thermo-responsibility under physiological conditions. Specifically disclosed are: a novel polylysine (particularly, poly(&egr;-L-lysine)) derivative having a 1,2-epoxyalkane (particularly, 1,2-epoxybutane) introduced therein; an aqueous composition comprising the derivative and having thermo-responsibility; and a method for condensing/separating an anionic compound by using the polylysine derivative.

IPC Classes  ?

  • C08G 69/48 - Polymers modified by chemical after-treatment
  • C08L 101/16 - Compositions of unspecified macromolecular compounds the macromolecular compounds being biodegradable

51.

LIQUID-CRYSTAL COMPOSITION AND LIQUID-CRYSTAL DISPLAY ELEMENT

      
Application Number JP2007062790
Publication Number 2008/018248
Status In Force
Filing Date 2007-06-26
Publication Date 2008-02-14
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Hattori, Norikatsu
  • Fujita, Hiroaki

Abstract

A liquid-crystal composition which satisfies at least one of properties including a high upper-limit temperature for the nematic phase, low lower-limit temperature for the nematic phase, low viscosity, high optical anisotropy, negatively high permittivity anisotropy, high specific resistance, high stability to ultraviolet, and high stability to heat or has a proper balance between at least two of those properties. The liquid-crystal composition comprises a first ingredient comprising at least one compound selected among compounds represented by the formulae (1-1) and (1-2) and a second ingredient comprising at least one compound selected among compounds represented by the formula (2) and has negative permittivity anisotropy. For example, R1, R2, R3, and R4 each is C1-12 alkyl; Z1, Z2, and Z3 each is a single bond or -(CH2)2-; and ring A is 1,4-cyclohexylene or 1,4-phenylene.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/02 - Liquid crystal materials characterised by optical, electrical or physical properties of the components, in general
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

52.

KIT FOR DETECTION/QUANTIFICATION OF ANALYTE, AND METHOD FOR DETECTION/QUANTIFICATION OF ANALYTE

      
Application Number JP2007063044
Publication Number 2008/001868
Status In Force
Filing Date 2007-06-28
Publication Date 2008-01-03
Owner
  • CHISSO CORPORATION (Japan)
  • Ortho-Clinical Diagnostics Kabushiki Kaisha (Japan)
Inventor
  • Nagaoka, Hirokazu
  • Ohnishi, Noriyuki
  • Matsui, Kageaki
  • Sugita, Satoru

Abstract

Disclosed are a detection/quantification kit and a detection/quantification method for detecting/quantifying an analyte rapidly at a low cost and in a simple manner. Specifically, disclosed is a kit for detecting an analyte in a sample, comprising a first conjugate and a second conjugate, wherein the first conjugate comprises a first substance comprising a stimuli-responsive polymer and a first affinity substance having affinity for the analyte and bound to the first substance, and the second conjugate comprises a second substance carrying an electrical charge and a second affinity substance having affinity for the analyte and bound to the second substance. The first and second affinity substances can bind to different sites on the analyte simultaneously.

IPC Classes  ?

  • G01N 33/553 - Metal or metal coated
  • G01N 33/543 - ImmunoassayBiospecific binding assayMaterials therefor with an insoluble carrier for immobilising immunochemicals

53.

METHOD OF CULTURING VASCULAR SMOOTH MUSCLE CELLS, CULTURE DEVICE AND MEDICAL MATERIAL OBTAINED BY THE CULTURE

      
Application Number JP2007060604
Publication Number 2007/138973
Status In Force
Filing Date 2007-05-24
Publication Date 2007-12-06
Owner CHISSO CORPORATION (Japan)
Inventor
  • Miyamoto, Keiichi
  • Horiuchi, Takashi

Abstract

It is intended to provide a method of culturing vascular smooth muscle cells while sustaining the normal function of the cells, a culture device therefor, and a material for regenerative medicine. In this method, use is made of the fact that vascular smooth muscle cells recognize elastin as an extracellular matrix and grow using the same. Namely, a method of culturing vascular smooth muscle cells on elastin; a culture device in which elastin is fixed on the surface where cells grow; a culture device in which the surface where cells grow comprises a molded article made of elastin; and a medical material which is obtained by culturing vascular smooth muscle cells by using such a culture device.

IPC Classes  ?

  • C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor
  • A61F 2/06 - Blood vessels
  • A61L 27/00 - Materials for prostheses or for coating prostheses
  • C12M 3/00 - Tissue, human, animal or plant cell, or virus culture apparatus
  • C12N 5/02 - Propagation of single cells or cells in suspensionMaintenance thereofCulture media therefor
  • C12N 5/07 - Animal cells or tissues
  • C12N 5/071 - Vertebrate cells or tissues, e.g. human cells or tissues
  • C12N 5/077 - Mesenchymal cells, e.g. bone cells, cartilage cells, marrow stromal cells, fat cells or muscle cells

54.

2-OXETANONE DERIVATIVE AND PROCESS FOR PRODUCTION THEREOF

      
Application Number JP2007060147
Publication Number 2007/135954
Status In Force
Filing Date 2007-05-17
Publication Date 2007-11-29
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Urata, Yasuo
  • Oshima, Shunji
  • Nishibata, Ryousuke
  • Kodaki, Keiichi
  • Takeuchi, Hiroyuki
  • Matsui, Shuichi

Abstract

An aldehyde derivative represented by the general formula (2) is reacted with ketene in the presence of a Lewis acid catalyst to synthesize a novel 2-oxetanone derivative (1). The 2-oxetanone derivative (1) is purified by recrystallization to produce a 2-oxetanone derivative having a high trans purity. The purified 2-oxetanone derivative is then converted into a vinyl derivative (3) by a decarboxylation reaction. (2) (1) (3)

IPC Classes  ?

  • C07D 305/12 - Beta-lactones
  • C07D 405/10 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
  • C07D 407/08 - Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings

55.

COMPLEX FOR USE IN THE SCREENING OF SUBSTANCE

      
Application Number JP2007058582
Publication Number 2007/125822
Status In Force
Filing Date 2007-04-20
Publication Date 2007-11-08
Owner
  • TOKYO INSTITUTE OF TECHNOLOGY (Japan)
  • CHISSO CORPORATION (Japan)
Inventor
  • Handa, Hiroshi
  • Sawa, Chika
  • Kabe, Yasuaki
  • Sakamoto, Satoshi
  • Nishio, Kousuke
  • Yung, Tetsu Mau Chit
  • Kuramori, Chikanori
  • Furukawa, Shoichiro
  • Inoue, Satoshi

Abstract

Disclosed is a complex comprising a carrier, a physiologically active substance and a protein, wherein the carrier binds to the physiologically active substance, the physiologically active substance has an affinity for the protein and binds to the protein by means of the affinity, and the protein is labeled with a light-emitting substance or a fluorescent substance. Also disclosed is a method for screening a substance by using the complex. The method enables to advantageously utilize a compound which can act on a disease-causing protein but cannot be used as a pharmaceutical agent because of its severe adverse side-effects and also enables to search for a substance with high efficiency.

IPC Classes  ?

  • G01N 33/542 - ImmunoassayBiospecific binding assayMaterials therefor with immune complex formed in liquid phase with steric inhibition or signal modification, e.g. fluorescent quenching
  • C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions
  • C12Q 1/32 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving oxidoreductase involving dehydrogenase
  • G01N 21/76 - ChemiluminescenceBioluminescence
  • G01N 21/78 - Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
  • G01N 33/15 - Medicinal preparations
  • G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing
  • G01N 33/543 - ImmunoassayBiospecific binding assayMaterials therefor with an insoluble carrier for immobilising immunochemicals
  • G01N 33/566 - ImmunoassayBiospecific binding assayMaterials therefor using specific carrier or receptor proteins as ligand binding reagent

56.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2007054196
Publication Number 2007/108307
Status In Force
Filing Date 2007-03-05
Publication Date 2007-09-27
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Fujita, Hiroaki
  • Hattori, Norikatsu

Abstract

This invention provides a liquid crystal composition, which has a broad nematic phase temperature range, has proper optical anisotropy, has large negative permittivity anisotropy, and has a large specific resistance value, a liquid crystal composition, which can increase optical anisotropy while satisfying the above properties and has a lower limit temperature in its nematic phase, preferably -20ºC or below, and a liquid crystal display element comprising this composition. The liquid crystal composition is a liquid crystal composition having negative permittivity anisotropy, comprising a first component, which is a liquid crystalline compound containing terphenyl in which one or two hydrogen atoms have been substituted by a fluorine atom, and a second component, which is a liquid crystalline compound containing phenylene in which two hydrogen atoms have been substituted by a halogen atom. The liquid crystal display element comprises this liquid crystal composition.

IPC Classes  ?

  • C09K 19/44 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups containing compounds with benzene rings directly linked
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

57.

LIQUID-CRYSTAL COMPOSITION AND LIQUID-CRYSTAL ELEMENT

      
Application Number JP2007055300
Publication Number 2007/105803
Status In Force
Filing Date 2007-03-09
Publication Date 2007-09-20
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
  • KYUSHU UNIVERSITY, NATIONAL UNIVERSITY CORPORATION (Japan)
Inventor
  • Haseba, Yasuhiro
  • Kikuchi, Yuji

Abstract

A liquid-crystal composition which comprises a compound (1) having a clear point of T1 and a compound (2) having a clear point of T2 and has a clear point of Tx. The amounts of the compound (1) and the compound (2) are 10-80 wt.% and 20-90 wt.%, respectively, based on the liquid-crystal composition. The clear point T1, the clear point T2, and the clear point Tx of the liquid-crystal composition satisfy T1>T2 and T1-Tx≥100°C. The liquid-crystal composition has an optically isotropic liquid-crystal phase and is for use in elements which are operated with an optically isotropic liquid-crystal phase.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/02 - Liquid crystal materials characterised by optical, electrical or physical properties of the components, in general
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/54 - Additives having no specific mesophase
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

58.

NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

      
Application Number JP2007051363
Publication Number 2007/086552
Status In Force
Filing Date 2007-01-29
Publication Date 2007-08-02
Owner CHISSO CORPORATION (Japan)
Inventor
  • Ono, Yohei
  • Uchida, Manabu

Abstract

Disclosed is a compound for an electron-transporting material and/or an electron injecting material, which contributes to decrease driving voltage of an organic EL device and to extend life of the organic EL device. Also disclosed is an organic EL device using such a compound. Specifically disclosed is a novel compound represented by the following formula (1). (1) In the formula, R1-R4 independently represent a hydrogen, an alkyl having 1-6 carbon atoms, a cycloalkyl having 3-6 carbon atoms, an optionally substituted aromatic ring having 6-18 carbon atoms or an optionally substituted heteroaromatic ring having 2-18 carbon atoms; R5-R8, R9, R10, R16 and R17 independently represent a hydrogen, an alkyl having 1-6 carbon atoms or a cycloalkyl having 3-6 carbon atoms; and R11-R15 and R18-R22 independently represent a hydrogen, an alkyl having 1-6 carbon atoms, a cycloalkyl having 3-6 carbon atoms, an optionally substituted aromatic ring having 6-18 carbon atoms or an optionally substituted heteroaromatic ring having 2-18 carbon atoms.

IPC Classes  ?

  • C07D 213/22 - Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing two or more pyridine rings directly linked together, e.g. bipyridyl
  • C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
  • H01L 51/50 - Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes (OLED) or polymer light emitting devices (PLED)

59.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2007050233
Publication Number 2007/083561
Status In Force
Filing Date 2007-01-11
Publication Date 2007-07-26
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Fujita, Hiroaki
  • Hattori, Norikatsu

Abstract

Disclosed is a liquid crystal composition which can form a nematic phase over a wide temperature range, has a low viscosity, a proper level of optical anisotropy, a high negative dielectric anisotropy, and a high specific resistance, preferably which is decreased in the lower limit of the nematic phase (the lower limit is preferably -20˚C or lower) while retaining the properties mentioned above. Also disclosed is a liquid crystal display element comprising the composition. The liquid crystal composition has a negative dielectric anisotropy and comprises a first component and a second component, wherein the first component comprises a liquid crystalline compound having an ethylene bond and a 2,3-difluorophenylene and the second component comprises a liquid crystalline compound having a phenylene in which two hydrogen atoms are substituted by halogen atoms.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

60.

MONOFLUORINATED TERPHENYL COMPOUND HAVING ALKENYL, LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2006325973
Publication Number 2007/077844
Status In Force
Filing Date 2006-12-26
Publication Date 2007-07-12
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Satou, Teizi
  • Kondou, Tomoyuki
  • Hattori, Norikatsu
  • Fujita, Hiroaki

Abstract

Disclosed is a liquid crystalline compound which is stable against heat and ultraviolet ray, has a low viscosity, a proper level of an anisotropic refractive index and a proper level of an anisotropic dielectric constant, can form a nematic phase over a wide temperature range, and has an excellent compatibility to other liquid crystal compound, particularly a liquid crystalline compound having a low viscosity. The liquid crystalline compound is represented by the general formula (1): (1) wherein R1 represents a hydrogen or an alkyl having 1 to 5 carbon atoms; one of X1 and X2 represents a hydrogen and the other represents a fluorine; and R2 represents a hydrogen or a methyl.

IPC Classes  ?

  • C07C 25/24 - Halogenated aromatic hydrocarbons with unsaturated side chains
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

61.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2006326054
Publication Number 2007/077872
Status In Force
Filing Date 2006-12-27
Publication Date 2007-07-12
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Fujita, Hiroaki
  • Hattori, Norikatsu

Abstract

Disclosed is a liquid crystal composition which can form a nematic phase over a wide temperature range, has a proper level of optical anisotropy, a high negative dielectric anisotropy, and a high specific resistance, preferably a liquid crystal composition in which the optical anisotropy can be increased and the lower limit of the nematic phase can be lowered while retaining the properties mentioned above. Also disclosed is a liquid crystal display element comprising the composition. The liquid crystal composition has a negative dielectric anisotropy and comprises a first component and a second component, wherein the first component comprises a liquid crystalline compound having a terphenyl structure in which one or two hydrogen atoms are substituted by fluorine atoms and the second component comprises a liquid crystalline compound having a phenylene which has hydrogen 2-substituted by fluorine.

IPC Classes  ?

  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

62.

COMPOUND HAVING HYDROCOUMARIN SKELETON, LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2006324546
Publication Number 2007/066755
Status In Force
Filing Date 2006-12-08
Publication Date 2007-06-14
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Goto, Mayumi
  • Sugiura, Teruyo
  • Hattori, Norikatsu
  • Sagou, Kouki

Abstract

A liquid crystal compound that is stable against heat, light, etc., having high clearing point and appropriate optical anisotropy, and that further has high negative dielectric constant anisotropy and high miscibility with other liquid crystal compounds; and a liquid crystal composition containing the above compound that has low viscosity, having appropriate optical anisotropy and appropriate negative dielectric constant anisotropy, and that exhibits low threshold value voltage, being high in the upper limit temperature of nematic phase (nematic phase-isotropic phase phase transition temperature) and low in the lower limit temperature of nematic phase. Compounds having hydrocoumarin skeletons are synthesized and liquid crystal compositions containing the compounds are prepared.

IPC Classes  ?

  • C07D 311/20 - Benzo [b] pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 hydrogenated in the hetero ring
  • C07D 311/76 - Benzo [c] pyrans
  • C07D 405/04 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • C07D 407/04 - Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • C07D 407/06 - Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
  • C07D 407/08 - Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing alicyclic rings
  • C07D 407/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/16 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon double bonds, e.g. stilbenes
  • C09K 19/18 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
  • C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/32 - Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
  • C09K 19/34 - Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • G02F 1/133 - Constructional arrangementsOperation of liquid crystal cellsCircuit arrangements

63.

ELECTRON TRANSPORTING MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME

      
Application Number JP2006317545
Publication Number 2007/029696
Status In Force
Filing Date 2006-09-05
Publication Date 2007-03-15
Owner CHISSO CORPORATION (Japan)
Inventor
  • Ono, Youhei
  • Tamada, Hiroshi
  • Kageyama, Akiko
  • Uchida, Manabu

Abstract

A compound represented by the formula (1):wherein G represents a n-valent linker group; n represents an integer of 2 to 4; R1 to R4 independently represent a hydrogen, a univalent group or a free atomic valency binding to the group G; and R5 to R8 independently represent a hydrogen or a univalent group; provided that any one of R1 to R4 is a free atomic valency binding to the group G, and n's 2,3'-bipyridyl groups may be the same as or different from one another. The compound is useful as an electron transporting material for an organic electroluminescent device. An organic electroluminescent device having the compound in the electron transporting layer shows a long operating life and a low driving voltage.

IPC Classes  ?

  • C07D 213/22 - Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing two or more pyridine rings directly linked together, e.g. bipyridyl
  • C07D 401/04 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
  • H01L 51/50 - Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes (OLED) or polymer light emitting devices (PLED)

64.

LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY DEVICE

      
Application Number JP2006304935
Publication Number 2006/098289
Status In Force
Filing Date 2006-03-13
Publication Date 2006-09-21
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Fujita, Hiroaki
  • Shimada, Teru
  • Hattori, Norikatsu

Abstract

A liquid crystal composition that is wide in nematic phase temperature range, having appropriate optical anisotropy, and that is large in negative dielectric constant anisotropy, being large in specific resistance; in particular, a liquid crystal composition that while satisfying these performance requirements, enables reducing of optical anisotropy and enables lowering of nematic phase lower-limit temperature, preferably lowering to ≤ -20°C; and a liquid crystal display device containing the above liquid crystal composition. There is provided a liquid crystal composition exhibiting a negative dielectric constant anisotropy, comprising a first component of liquid crystal compound having a group of benzene ring having its two adjacent hydrogen atoms replaced by fluorine and chlorine as a group of cyclic structure and a second component of nonhalogenous liquid crystal compound with specified structure. Further, there is provided a liquid crystal display device containing this liquid crystal composition.

IPC Classes  ?

  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • C09K 19/42 - Mixtures of liquid crystal compounds covered by two or more of the preceding groups
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

65.

CHLOROFLUOROBENZENE LIQUID CRYSTALLINE COMPOUND, LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY ELEMENT

      
Application Number JP2006303869
Publication Number 2006/093189
Status In Force
Filing Date 2006-03-01
Publication Date 2006-09-08
Owner
  • CHISSO CORPORATION (Japan)
  • CHISSO PETROCHEMICAL CORPORATION (Japan)
Inventor
  • Goto, Yasuyuki
  • Shimada, Teru
  • Sugiura, Teruyo

Abstract

This invention provides liquid crystalline compounds, which are stable against heat, light and the like, can exhibit a nematic phase in a broad temperature range, have low viscosity, have proper optical anisotropy, and proper elastic constants K33 and K11, wherein K33: bending modulus of elasticity and K11: splay modulus of elasticity, and further have a proper negative permittivity anisotropy and excellent compatibility with other liquid crystalline compounds. There are also provided a liquid crystalline composition using this liquid crystalline compound and a liquid crystal display element using this liquid crystalline composition. The liquid crystalline compounds are represented by formulae (a) to (b): (a) (b) (c) (d) wherein, for example, Ra and Rb each independently represent a straight chain alkyl or a straight chain alkoxy; rings A1, A2, B and C each independently represent trans-1,4-cyclohexylene or 1,4-phenylene; Z11, Z12, Z2, and Z3 each independently represent a single bond or alkylene; and one of X1 and X2 represents fluorine and the other represents chlorine.

IPC Classes  ?

  • C07C 25/13 - Monocyclic aromatic halogenated hydrocarbons containing fluorine
  • C07C 25/18 - Polycyclic aromatic halogenated hydrocarbons
  • C07C 43/174 - Unsaturated ethers containing halogen containing six-membered aromatic rings
  • C07C 43/192 - Ethers having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring containing halogen
  • C07C 43/225 - Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
  • C09K 19/12 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
  • C09K 19/14 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
  • C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
  • G02F 1/13 - Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulatingNon-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells

66.

Polypropylene composition

      
Application Number 09795310
Status Pending
Filing Date 2001-03-01
First Publication Date 2001-10-18
Owner Chisso Corporation (USA)
Inventor
  • Ushioda, Tsutomu
  • Yahata, Tsuyoshi

Abstract

Provided is a polypropylene composition which is a molding material having good flexibility and good elastic recovery. The polypropylene composition comprises from 1 to 99% by weight of elastomeric polypropylene obtained through (co)polymerization of propylene or propylene and olefin except propylene in the presence of a metallocene catalyst (A) that comprises a metallocene compound (A), an activator compound and optionally an organoaluminum compound, or of a supported metallocene catalyst (A) that comprises the metallocene catalyst (A) supported on a particulate carrier, or of a catalyst that comprises tetraneophyl zirconium supported on alumina, and from 1 to 99% by weight of atactic polypropylene totaling 100% by weight.