Abstract

A lubricating oil composition for two-wheeled motor vehicles including a base oil and a metal phenate and having a coefficient of friction measured of less than 0.0900. The lubricating oil composition in which a performance required for lubricating oil for engines is satisfied, and a good shift feeling is achieved while a high coefficient of friction is kept in a wet clutch.

IPC Classes  ?

• C10M 129/02 - Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
• C10M 159/00 - Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
• C10M 169/04 - Mixtures of base-materials and additives
• C10N 10/04 - Groups 2 or 12
• C10N 30/02 - Pour-pointViscosity index
• C10N 40/04 - Oil-bathGear-boxesAutomatic transmissionsTraction drives
• C10N 40/25 - Internal-combustion engines

Abstract

A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom. A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom.

IPC Classes  ?

• C07D 493/00 - Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 85/40 - Organosilicon compounds, e.g. TIPS pentacene
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/10 - Triplet emission

Abstract

MAXMAXMAX (EM) of the organic luminescent material are different from each other; the minimum excitation triplet energy of each of the two or more triplet sensitizers is not lower than the minimum excitation triplet energy of the organic luminescent material; and the minimum excitation singlet energy of each of the two or more triplet sensitizers is lower than the minimum excitation singlet energy of the organic luminescent material.

IPC Classes  ?

• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• G02B 5/20 - Filters

Abstract

A compound represented by a formula (1C-A) below. A compound represented by a formula (1C-A) below. A compound represented by a formula (1C-A) below. One of R4 to R8 and R10 to R12 is a group represented by a formula (1D-A) above; R1 to R3, R9, and R4 to R8 and R10 to R12 not being the group represented by the formula (1D-A) are each a hydrogen atom, a substituent, or the like; at least one of R21 to R30 is other than a hydrogen atom; when R11 is a group represented by a formula (1D), R12 is a hydrogen atom or a phenyl group; when R12 is a group represented by the formula (1D), R11 is a hydrogen atom or a phenyl group; in the formula (1D), one of R21 to R30 represents a bonding position to a benz[a]anthracene ring in the formula (1C), and R21 to R30 not being the bonding position are each a hydrogen atom, a substituent, or the like.

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07C 15/20 - Polycyclic condensed hydrocarbons
• C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants

Abstract

A sulfide solid electrolyte may be able to adjust the morphology unavailable traditionally, or readily adjust so as to have a desired morphology. Such a sulfide solid electrolyte may include a substance including a lithium element, a sulfur element, and a phosphorus element; and an amine compound. The solid electrolyte may have a volume-based average particle diameter of 10 μm or less, measured by laser diffraction particle size distribution measurement, and/or a BET specific surface area of 40 m2/g or less.

IPC Classes  ?

• H01M 10/0562 - Solid materials
• H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
• H01M 10/42 - Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells

Abstract

A compound is represented by a formula (1A-A). One of R4 to R8 and R10 to R12 is a group represented by a formula (1B-A1), (1B-A2), or (1B-A3) above; R1 to R3, R9, and R4 to R8 and R10 to R12 other than the above are each a hydrogen atom, a substituent, or the like; when R11 or R12 is a group represented by the formula (1B-A1), (1B-A2), or (1B-A3), R12 or R11 is a hydrogen atom or a phenyl group; and in the formulae (1B-A1) to (1B-A3), R51 to R57, R61 to R64, R71 to R74, and R81 to R84 forming no ring in the formulae (1B-A1) to (1B-A3) are each a hydrogen atom, a substituent, or the like; and * represents a bonding position to a benz[a]anthracene ring in the formula (1A-A). A compound is represented by a formula (1A-A). One of R4 to R8 and R10 to R12 is a group represented by a formula (1B-A1), (1B-A2), or (1B-A3) above; R1 to R3, R9, and R4 to R8 and R10 to R12 other than the above are each a hydrogen atom, a substituent, or the like; when R11 or R12 is a group represented by the formula (1B-A1), (1B-A2), or (1B-A3), R12 or R11 is a hydrogen atom or a phenyl group; and in the formulae (1B-A1) to (1B-A3), R51 to R57, R61 to R64, R71 to R74, and R81 to R84 forming no ring in the formulae (1B-A1) to (1B-A3) are each a hydrogen atom, a substituent, or the like; and * represents a bonding position to a benz[a]anthracene ring in the formula (1A-A).

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07D 307/92 - NaphthofuransHydrogenated naphthofurans
• C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
• H10K 50/13 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light comprising stacked EL layers within one EL unit

Abstract

The present invention provides: a crystalline sulfide solid electrolyte which contains lithium atoms, phosphorus atoms, sulfur atoms, and halogen atoms, is excellent in battery lifetime characteristics and voltage resistance, also has excellent coatability, and has an elastic dissipation energy, calculated from a focus curve measured by an atomic force microscopy, of 5.0×10-18 J or more; and a method for manufacturing the same.

IPC Classes  ?

• H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
• H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
• H01B 13/00 - Apparatus or processes specially adapted for manufacturing conductors or cables
• H01M 10/0562 - Solid materials

Abstract

An organic electroluminescence device includes an anode, a cathode, and an emitting region disposed between the anode and the cathode, in which the emitting region includes a first emitting layer and a second emitting layer, the first emitting layer contains a first compound represented by a formula below, and the second emitting layer contains a second compound. An organic electroluminescence device includes an anode, a cathode, and an emitting region disposed between the anode and the cathode, in which the emitting region includes a first emitting layer and a second emitting layer, the first emitting layer contains a first compound represented by a formula below, and the second emitting layer contains a second compound. An organic electroluminescence device includes an anode, a cathode, and an emitting region disposed between the anode and the cathode, in which the emitting region includes a first emitting layer and a second emitting layer, the first emitting layer contains a first compound represented by a formula below, and the second emitting layer contains a second compound. At least one of R101 to R112 in the formula (100A), L101 or Ar101 in the formula (100B) has at least one deuterium atom. When only L101 has at least one deuterium atom, the at least one deuterium atom is bonded to a ring that is of rings forming L1 and directly bonded to a benz[a]anthracene ring in the formula (100A).

IPC Classes  ?

• C07D 307/91 - DibenzofuransHydrogenated dibenzofurans
• C07B 59/00 - Introduction of isotopes of elements into organic compounds
• C07C 13/547 - Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings at least one ring not being six-membered, the other rings being at the most six-membered
• C07C 15/38 - Polycyclic condensed hydrocarbons containing four rings
• C07D 209/90 - Benzo [c, d] indolesHydrogenated benzo [c, d] indoles
• C07D 333/76 - Dibenzothiophenes
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 85/20 - Carbon compounds, e.g. carbon nanotubes or fullerenes
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/10 - Triplet emission

Abstract

A refrigerator oil composition used in a refrigerant containing one or more unsaturated fluorinated hydrocarbon compounds selected from compounds represented by the following general formula (1): CxFyHz (1), wherein x is an integer of 2 to 6, y is an integer of 1 to 11, z is an integer of 1 to 11, and there are one or more carbon-carbon unsaturated bonds in the molecule, the refrigerator oil composition containing a base oil (A) that includes polyvinyl ether, a modified silicone compound (B), and a specific epoxy compound (C).

IPC Classes  ?

• C09K 5/04 - Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice-versa

Abstract

A lubricating oil composition may have excellent fuel economy and high shear stability. Such a lubricating oil composition may include: a comb-like polymer (A1) having a weight average molecular weight (Mw) of less than 300,000; and a comb-like polymer (A2) having a Mw of at least 400,000. The (A1)/(A2) mass content ratio of the comb-like polymer (A1) to the comb-like polymer (A2) in terms of resin content may be at least 0.25.

IPC Classes  ?

• C10M 171/04 - Specified molecular weight or molecular weight distribution
• C10M 159/00 - Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
• C10M 169/04 - Mixtures of base-materials and additives
• C10N 20/02 - ViscosityViscosity index
• C10N 30/00 - Specified physical or chemical property which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
• C10N 40/25 - Internal-combustion engines

Abstract

A sulfide solid electrolyte that contains lithium, phosphorus, sulfur, chlorine and bromine, wherein in powder X-ray diffraction analysis using CuKα rays, it has a diffraction peak A at 2θ=25.2±0.5 deg and a diffraction peak B at 2θ=29.7±0.5 deg, the diffraction peak A and the diffraction peak B satisfy the following formula (A), and a molar ratio of the chlorine to the phosphorus “c (Cl/P)” and a molar ratio of the bromine to the phosphorus “d (Br/P)” satisfies the following formula (1): A sulfide solid electrolyte that contains lithium, phosphorus, sulfur, chlorine and bromine, wherein in powder X-ray diffraction analysis using CuKα rays, it has a diffraction peak A at 2θ=25.2±0.5 deg and a diffraction peak B at 2θ=29.7±0.5 deg, the diffraction peak A and the diffraction peak B satisfy the following formula (A), and a molar ratio of the chlorine to the phosphorus “c (Cl/P)” and a molar ratio of the bromine to the phosphorus “d (Br/P)” satisfies the following formula (1): 1.2 < c + d < 1.9 ( 1 ) 0.845 < S A / S B < 1.2 ( A ) A sulfide solid electrolyte that contains lithium, phosphorus, sulfur, chlorine and bromine, wherein in powder X-ray diffraction analysis using CuKα rays, it has a diffraction peak A at 2θ=25.2±0.5 deg and a diffraction peak B at 2θ=29.7±0.5 deg, the diffraction peak A and the diffraction peak B satisfy the following formula (A), and a molar ratio of the chlorine to the phosphorus “c (Cl/P)” and a molar ratio of the bromine to the phosphorus “d (Br/P)” satisfies the following formula (1): 1.2 < c + d < 1.9 ( 1 ) 0.845 < S A / S B < 1.2 ( A ) where SA is an area of the diffraction peak A and SB is an area of the diffraction peak B.

IPC Classes  ?

• H01M 10/0562 - Solid materials
• H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
• H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
• H01M 4/136 - Electrodes based on inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy
• H01M 4/58 - Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFySelection of substances as active materials, active masses, active liquids of polyanionic structures, e.g. phosphates, silicates or borates
• H01M 10/052 - Li-accumulators
• H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodesLithium-ion batteries
• H01M 10/058 - Construction or manufacture

Abstract

Provided is a compound that improves the performance of an organic EL element, the compound being represented by formula (1) and containing at least one deuterium atom in a molecule. (The symbols in the formula are as defined in the specification.)

IPC Classes  ?

• C07D 307/77 - Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

A thin film transistor includes an oxide semiconductor layer having a polycrystalline structure over a substrate, a gate electrode over the oxide semiconductor layer, and a gate insulating layer between the oxide semiconductor layer and the gate electrode. The oxide semiconductor layer includes a first region having a first carrier concentration and overlapping the gate electrode, a second region having a second carrier concentration and not overlapping the gate electrode, and a third region between the first region and the second region and overlapping the gate electrode. The second carrier concentration is larger than the first carrier concentration. A carrier concentration of the third region decreases from the second region to the first region in a channel length direction. A length of the third region is greater than or equal to 0.00 μm and less than or equal to 0.60 μm in the channel length direction.

IPC Classes  ?

• H01L 29/786 - Thin-film transistors
• H01L 29/04 - Semiconductor bodies characterised by their crystalline structure, e.g. polycrystalline, cubic or particular orientation of crystalline planes
• H01L 29/06 - Semiconductor bodies characterised by the shapes, relative sizes, or dispositions of the semiconductor regions
• H01L 29/49 - Metal-insulator semiconductor electrodes

Abstract

Provided is a method for producing sulfide solid electrolyte having an argyrodite-type crystal structure, the method including mixing lithium sulfide, a phosphorus sulfide, and an ammonium halide to produce a solid electrolyte precursor, and firing the solid electrolyte precursor. The method for producing a sulfide solid electrolyte having an argyrodite-type crystal structure provides a method for easily producing a high-quality sulfide solid electrolyte without using an elemental halogen which complicates the handling or a lithium halide which has a considerably high hygroscopicity.

IPC Classes  ?

• H01M 10/0562 - Solid materials

Abstract

The present invention provides a sulfide solid electrolyte mixture which contains: a sulfide solid electrolyte that contains lithium atoms, sulfur atoms, and phosphorus atoms, the sulfide solid electrolyte having a high ion conductivity and being easily densified when compressed; and an electrolyte solution that contains a lithium salt and an ionic liquid. With respect to this sulfide solid electrolyte mixture, the product of (A) the number of moles of the lithium salt in 1 liter of the electrolyte solution and (B) the content (mass%) of the electrolyte solution based on the total amount of the sulfide solid electrolyte mixture is 11 or more.

IPC Classes  ?

• H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
• H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
• H01M 4/13 - Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulatorsProcesses of manufacture thereof
• H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
• H01M 10/052 - Li-accumulators
• H01M 10/056 - Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes

Abstract

A radio wave absorber comprising a resin and a carbon filler, wherein 60 to 90% by volume of the total carbon filler is present in a region from the first surface of the radio wave absorber to half of the total thickness of the radio wave absorber.

IPC Classes  ?

• H01Q 17/00 - Devices for absorbing waves radiated from an antenna Combinations of such devices with active antenna elements or systems

Abstract

An electrode having a structure in which a plurality of layers including a sulfur-based active material, a conductive assistant, and a solid electrolyte are laminated, wherein: the conductive assistant is a carbon material; and, in the plurality of layers, the ratio of the content of the solid electrolyte with respect to the content of the conductive assistant becomes higher from a layer of one end side toward a layer of the other end side in the lamination direction, and the content of the conductive assistant throughout the entirety of the plurality of layers is 10-30 mass%.

IPC Classes  ?

• H01M 4/13 - Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulatorsProcesses of manufacture thereof
• H01M 4/38 - Selection of substances as active materials, active masses, active liquids of elements or alloys
• H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
• H01M 10/052 - Li-accumulators
• H01M 10/0562 - Solid materials
• H01M 10/0585 - Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators

Goods & Services

Coolants; dielectric fluids as a chemical preparation for cooling computer servers, except oils. Cooling lubricants; dielectric oils for cooling computer servers.

Abstract

An organic EL device includes an emitting region and a first anode side organic layer. The first anode side organic layer contains a first material. The emitting region includes a first emitting layer containing first and second host materials and a second emitting layer containing a third host material. Energy levels of highest occupied molecular orbitals of the first material, the first host material, and the second host material HOMO(HT1), HOMO(H1), and HOMO(H2) satisfy a relationship of a numerical formula (Numerical Formula A1) below, and triplet energies of the first host material, the second host material, and the third host material T1(H1), T1(H2), and T1(H3) satisfy relationships of numerical formulae (Numerical Formula A2 and Numerical Formula A3) below, An organic EL device includes an emitting region and a first anode side organic layer. The first anode side organic layer contains a first material. The emitting region includes a first emitting layer containing first and second host materials and a second emitting layer containing a third host material. Energy levels of highest occupied molecular orbitals of the first material, the first host material, and the second host material HOMO(HT1), HOMO(H1), and HOMO(H2) satisfy a relationship of a numerical formula (Numerical Formula A1) below, and triplet energies of the first host material, the second host material, and the third host material T1(H1), T1(H2), and T1(H3) satisfy relationships of numerical formulae (Numerical Formula A2 and Numerical Formula A3) below, HOMO ⁡ ( HT ⁢ 1 ) > HOMO ⁡ ( H ⁢ 2 ) > HOMO ⁡ ( H ⁢ 1 ) ( Numerical ⁢ Formula ⁢ A1 ) T 1 ( H ⁢ 1 ) > T 1 ( H ⁢ 3 ) ( Numerical ⁢ Formula ⁢ A2 ) T 1 ( H ⁢ 2 ) > T 1 ( H ⁢ 3 ) . ( Numerical ⁢ Formula ⁢ A3 )

IPC Classes  ?

• H10K 85/20 - Carbon compounds, e.g. carbon nanotubes or fullerenes
• C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 85/40 - Organosilicon compounds, e.g. TIPS pentacene
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/00 - Properties of the organic materials covered by group
• H10K 101/10 - Triplet emission
• H10K 101/30 - Highest occupied molecular orbital [HOMO], lowest unoccupied molecular orbital [LUMO] or Fermi energy values

Abstract

A lignin composition containing two or more compounds represented by formula (1), wherein the total amount of the compounds is 0.50 mass% or more.

IPC Classes  ?

• C08L 97/00 - Compositions of lignin-containing materials
• C08L 21/00 - Compositions of unspecified rubbers
• C08L 101/00 - Compositions of unspecified macromolecular compounds

Goods & Services

Measuring or testing machines and instruments; telecommunication machines and apparatus; personal digital assistants [PDAs]; computer software; computer operating programs; electronic components; downloadable text data; electronic publications; downloadable image files; animated cartoons; downloadable sticker images.

Abstract

1B8B111A112A113A113A is a group represented by general formula (B11).)

IPC Classes  ?

• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• C07D 307/77 - Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/13 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light comprising stacked EL layers within one EL unit
• H10K 50/15 - Hole transporting layers
• H10K 50/17 - Carrier injection layers
• H10K 50/18 - Carrier blocking layers
• H10K 50/858 - Arrangements for extracting light from the devices comprising refractive means, e.g. lenses
• H10K 59/10 - OLED displays
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/40 - Interrelation of parameters between multiple constituent active layers or sublayers, e.g. HOMO values in adjacent layers

Abstract

111181111213121313 is a group represented by general formula (12D).

IPC Classes  ?

• C07F 5/02 - Boron compounds
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 85/30 - Coordination compounds
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/20 - Delayed fluorescence emission

Abstract

A viscosity index improver composition which has an excellent viscosity index improving effect. A viscosity index improver composition which includes a poly(meth)acrylate (A) including a constituent unit (Y) derived from a monomer (y) having a diol functional group, and a poly(meth)acrylate (B) including a constituent unit (Z) derived from a monomer (z) having a boronic acid ester.

IPC Classes  ?

• C10M 169/04 - Mixtures of base-materials and additives
• C10M 145/14 - AcrylateMethacrylate
• C10M 155/04 - Monomer containing boron
• C10M 157/10 - Lubricating compositions characterised by the additive being a mixture of two or more macromolecular compounds covered by more than one of the main groups , each of these compounds being essential at least one of them being a compound containing atoms of elements not provided for in groups
• C10N 20/04 - Molecular weightMolecular weight distribution
• C10N 30/02 - Pour-pointViscosity index

Abstract

34112122|) is less than 0.5°.

IPC Classes  ?

• H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
• C01B 25/455 - Phosphates containing halogen
• H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
• H01B 1/08 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances oxides
• H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
• H01M 10/052 - Li-accumulators
• H01M 10/0562 - Solid materials

Abstract

19111011112131213GKGKHIJHIJJ is a substituent other than alkyl groups.

IPC Classes  ?

• C07F 5/02 - Boron compounds
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 85/30 - Coordination compounds

Abstract

A compound represented by a formula (1). A compound represented by a formula (1). A compound represented by a formula (1). In the formula (1): X1 to X4 are each independently a nitrogen atom or CRx; at least one of X1 to X4 is a nitrogen atom; a ring A, a ring B, and a ring C are each independently an aromatic hydrocarbon ring or a heterocycle; Ar1 is a hydrogen atom, an aryl group, or a group represented by a formula (2); and Ar2 is an aryl group or a group represented by a formula (3).

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07D 471/04 - Ortho-condensed systems
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 101/25 - Delayed fluorescence emission using exciplex
• H10K 101/30 - Highest occupied molecular orbital [HOMO], lowest unoccupied molecular orbital [LUMO] or Fermi energy values

Abstract

A method of producing a sulfide solid electrolyte having high ionic conductivity and high thermal stability without complicating the production process is provided, by a method of producing a sulfide solid electrolyte containing: mixing a raw material inclusion containing at least one type selected from a lithium atom, a sulfur atom, and a phosphorus atom, and a complexing agent having 2 or more of hetero atoms in the molecule to obtain an electrolyte precursor; mixing the electrolyte precursor in a solvent containing an oxygen atom-containing compound having a relative permittivity of 3.2 or higher at 25° C.; obtaining a grinding treatment product by performing grinding treatment of the mixture; and removing the solvent from the grinding treatment product to obtain a sulfide solid electrolyte.

IPC Classes  ?

• C01D 15/00 - Lithium compounds
• H01M 10/0562 - Solid materials

Abstract

Provided are: a compound represented by formula (1) (the symbols in the formula being as defined in the specification); a material, comprising the compound, for an organic electroluminescent element; an organic electroluminescent element comprising the compound; and an electronic device comprising the organic electroluminescent element.

IPC Classes  ?

• C07D 307/77 - Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
• C07D 307/91 - DibenzofuransHydrogenated dibenzofurans
• C07D 405/12 - 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 chain containing hetero atoms as chain links
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 50/17 - Carrier injection layers
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

A compound represented by the following formula (1). A compound represented by the following formula (1).

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• 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 251/24 - Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
• C07D 403/10 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings
• 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
• H10K 50/16 - Electron transporting layers

Abstract

The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device. The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device. The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device. wherein at least one of R1, R2, R3 and R4 represents an alkyl group having from 1 to 20 carbon atoms which is unsubstituted or substituted or an amino group NR84R85, and at least one of R5, R6, R7 and R8 represents an aryl group having from 6 to 30 ring carbon atoms which is unsubstituted or substituted; or a heteroaryl group having from 5 to 30 ring atoms which is unsubstituted or substituted, whereby the aryl group or the heteroaryl group may bind back to an adjacent residue and form a ring structure; Y1 and Y2 each independently represents RY or a group of formula (II) The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device. wherein at least one of R1, R2, R3 and R4 represents an alkyl group having from 1 to 20 carbon atoms which is unsubstituted or substituted or an amino group NR84R85, and at least one of R5, R6, R7 and R8 represents an aryl group having from 6 to 30 ring carbon atoms which is unsubstituted or substituted; or a heteroaryl group having from 5 to 30 ring atoms which is unsubstituted or substituted, whereby the aryl group or the heteroaryl group may bind back to an adjacent residue and form a ring structure; Y1 and Y2 each independently represents RY or a group of formula (II) The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device. wherein at least one of R1, R2, R3 and R4 represents an alkyl group having from 1 to 20 carbon atoms which is unsubstituted or substituted or an amino group NR84R85, and at least one of R5, R6, R7 and R8 represents an aryl group having from 6 to 30 ring carbon atoms which is unsubstituted or substituted; or a heteroaryl group having from 5 to 30 ring atoms which is unsubstituted or substituted, whereby the aryl group or the heteroaryl group may bind back to an adjacent residue and form a ring structure; Y1 and Y2 each independently represents RY or a group of formula (II) wherein at least one of Y1 and Y2 is a group of formula (II).

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07F 5/02 - Boron compounds
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants

Abstract

A lubricating oil composition, including: a base oil including an ester base oil and a hindered amine compound, where a content of the hindered amine compound is from 0.60 mass % to 10.0 mass % based on a total amount of the lubricating oil composition. An internal combustion engine installed in a hybrid system, the internal combustion engine filled with the lubricating oil composition. A method of lubricating an internal combustion engine installed a hybrid system, including: applying the lubricating oil composition to the internal combustion engine.

IPC Classes  ?

• C10M 169/04 - Mixtures of base-materials and additives
• C10M 101/02 - Petroleum fractions
• C10M 105/38 - Esters of polyhydroxy compounds
• C10M 111/02 - Lubricating compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups , each of these compounds being essential at least one of them being a non-macromolecular organic compound
• C10M 133/40 - Six-membered ring containing nitrogen and carbon only
• C10N 30/04 - Detergent or dispersant property
• C10N 30/10 - Inhibition of oxidation, e.g. anti-oxidants
• C10N 40/25 - Internal-combustion engines

Abstract

A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom. A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom.

IPC Classes  ?

• C07D 493/00 - Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 85/40 - Organosilicon compounds, e.g. TIPS pentacene
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/10 - Triplet emission

Abstract

A photoelectric conversion element includes a light absorbing layer, a hole transport layer that transports holes generated by photoexcitation of the light absorbing layer, and a transparent conductive layer that is in contact with the hole transport layer and receives holes from the hole transport layer. The carrier density of the transparent conductive layer is more than 1×1016 cm−3 and 1×1020 cm−3 or less.

IPC Classes  ?

• H10K 30/40 - Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising a p-i-n structure, e.g. having a perovskite absorber between p-type and n-type charge transport layers
• H10K 30/57 - Photovoltaic [PV] devices comprising multiple junctions, e.g. tandem PV cells
• H10K 30/86 - Layers having high hole mobility, e.g. hole-transporting layers or electron-blocking layers
• H10K 71/10 - Deposition of organic active material
• H10K 85/30 - Coordination compounds

Abstract

177K177K77K(M2) < 0.3eV. (In general formula (1): each of X1to X4independently is a nitrogen atom or CRx, provided that at least one of X1to X4is a nitrogen atom; and Ar1 is a hydrogen atom, a substituted or unsubstituted aryl group, or a group represented by general formula (2)).

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07D 471/04 - Ortho-condensed systems
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 101/20 - Delayed fluorescence emission

Abstract

Provided is a thermosetting composition which contains components (A), (B) and (C) and also contains one or more components selected from the group consisting of components (D) to (F). The content of components having a melting point of -5°C or higher among components (A) and (D) to (F) is 40 mass% or more relative to the total amount of components (A) and (D) to (F).　(A) A substituted or unsubstituted monofunctional or polyfunctional (meth)acrylate compound which has a group having an alicyclic hydrocarbon group with 6 or more ring-forming carbon atoms as an ester substituent group and which has a viscosity at 25°C of 1 to 300 mPa·s. (B) Spherical silica. (C) A pigment or dye. (D) (Meth)acrylic acid or a monofunctional (meth)acrylate compound having a polar group as an ester substituent group. (E) A monofunctional (meth)acrylate compound having a group other than the ester substituent group in component (A) and the ester substituent group in component (D) as an ester substituent group. (F) A polyfunctional (meth)acrylate compound having a group other than the ester substituent group in component (A) as an ester substituent group

IPC Classes  ?

• C08F 2/44 - Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
• C08F 20/00 - Homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide, or nitrile thereof
• C08F 292/00 - Macromolecular compounds obtained by polymerising monomers on to inorganic materials
• C08F 293/00 - Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
• C08K 3/013 - Fillers, pigments or reinforcing additives
• C08K 3/36 - Silica
• C08K 7/00 - Use of ingredients characterised by shape
• C08K 9/06 - Ingredients treated with organic substances with silicon-containing compounds
• C08L 33/00 - Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereofCompositions of derivatives of such polymers
• C08L 51/10 - Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers grafted on to inorganic materials
• C08L 53/00 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers

Abstract

Provided is a photoelectric conversion element capable of maintaining photoelectric conversion element performance under a high-temperature and high-humidity environment. A photoelectric conversion element (10) comprises: at least one photoelectric conversion layer (26); a conductive layer (24) electrically connected to the photoelectric conversion layer; a first sealing layer (40) on the conductive layer; and a second sealing layer (41) on the first sealing layer. The first sealing layer (40) contains at least one from among an inorganic metal oxide, an inorganic metal nitride, an inorganic metal oxynitride, and an inorganic metal fluoride. The second sealing layer (41) includes a polymer layer or a nitride coating layer.

IPC Classes  ?

• H01L 31/048 - Encapsulation of modules
• H02S 10/40 - Mobile PV generator systems

Abstract

222222222222/CO ratio in accordance with a desired synthetic chemical product.

IPC Classes  ?

• C25B 15/023 - Measuring, analysing or testing during electrolytic production
• C25B 1/04 - Hydrogen or oxygen by electrolysis of water
• C25B 1/23 - Carbon monoxide or syngas
• C25B 9/00 - Cells or assemblies of cellsConstructional parts of cellsAssemblies of constructional parts, e.g. electrode-diaphragm assembliesProcess-related cell features
• C25B 9/21 - Cells comprising dimensionally-stable non-movable electrodesAssemblies of constructional parts thereof with diaphragms two or more diaphragms
• C25B 13/08 - DiaphragmsSpacing elements characterised by the material based on organic materials

Abstract

Provided is a thermosetting composition containing components (A) to (C) below, a component (G) below, and one or more compounds selected from the group consisting of components (D) to (F) below.　(A) a monofunctional or polyfunctional (meth)acrylate compound that has, as an ester substituent, a group having a substituted or unsubstituted alicyclic hydrocarbon group having 6 or more ring-forming carbon atoms, and that has a viscosity of 1-300 mPa·s at 25°C; (B) a spherical silica; (C) a black pigment or a black dye; (D) a monofunctional (meth)acrylate compound having, as an ester substituent, a group having a (meth)acrylic acid or a polar group; (E) a monofunctional (meth)acrylate compound having, as an ester substituent, a group other than the ester substituent of the component (A) and the ester substituent of the component (D); (F) a polyfunctional (meth)acrylate compound having, as an ester substituent, a group other than the ester substituent of the component (A); and (G) a block copolymer containing at least one each of a block comprising a repeating unit represented by formula (G1) and a block comprising a repeating unit represented by formula (G2)

IPC Classes  ?

• C08F 2/44 - Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
• C08F 20/00 - Homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide, or nitrile thereof
• C08F 287/00 - Macromolecular compounds obtained by polymerising monomers on to block polymers
• C08F 292/00 - Macromolecular compounds obtained by polymerising monomers on to inorganic materials
• C08F 293/00 - Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
• C08K 3/013 - Fillers, pigments or reinforcing additives
• C08K 3/36 - Silica
• C08K 9/06 - Ingredients treated with organic substances with silicon-containing compounds
• C08L 33/00 - Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereofCompositions of derivatives of such polymers
• C08L 51/10 - Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers grafted on to inorganic materials
• C08L 53/00 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers

Abstract

Disclosed is a thermosetting composition which contains the components (A) to (C) described below, the component (G) described below, and one or more components selected from the group consisting of the components (D) to (F) described below.　(A) a monofunctional or polyfunctional (meth)acrylate compound which has, as an ester substituent, a group having a substituted or unsubstituted alicyclic hydrocarbon group having 6 or more ring carbon atoms, and which has a viscosity of 1-300 mPa∙s at 25°C (B) a spherical silica (C) a white pigment (D) a (meth)acrylic acid or a monofunctional (meth)acrylate compound which has, as an ester substituent, a group having a polar group (E) a monofunctional (meth)acrylate compound which has, as an ester substituent, a group other than the ester substituent of the component (A) and the ester substituent of the component (D) (F) a polyfunctional (meth)acrylate compound which has, as an ester substituent, a group other than the ester substituent of the component (A) (G) a block copolymer which contains at least one block composed of repeating units represented by formula (G1) and at least one block composed of repeating units represented by formula (G2)

IPC Classes  ?

• C08F 2/44 - Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
• C08F 20/00 - Homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide, or nitrile thereof
• C08F 287/00 - Macromolecular compounds obtained by polymerising monomers on to block polymers
• C08F 292/00 - Macromolecular compounds obtained by polymerising monomers on to inorganic materials
• C08F 293/00 - Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
• C08K 3/013 - Fillers, pigments or reinforcing additives
• C08K 3/36 - Silica
• C08K 9/06 - Ingredients treated with organic substances with silicon-containing compounds
• C08L 33/00 - Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereofCompositions of derivatives of such polymers
• C08L 51/10 - Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers grafted on to inorganic materials
• C08L 53/00 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers

Abstract

A continuous organic matter pyrolysis device includes: a charging section that continuously charges an organic matter; a vertical vessel for accommodating the organic matter charged from the charging section, a stirring means that is provided in the vertical vessel and that stirs the organic matter, a first heating means that heats the vertical vessel to pyrolyze and gasify the organic matter, a lead-out section connected to an upper portion of the vertical vessel and including a lead-out path through which the pyrolysis gas of the organic matter is led out, and a discharging section connected to a lower portion of the vertical vessel and including a discharge path through which an organic matter residue is continuously discharged.

IPC Classes  ?

• C08J 11/12 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by dry-heat treatment only
• C10B 53/07 - Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of synthetic polymeric materials, e.g. tyres
• C10G 1/10 - Production of liquid hydrocarbon mixtures from oil shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal from rubber or rubber waste

Abstract

A lubricant base oil for use in the preparation of a cooling lubricant composition, may have a % CP of 60 or more, and the dynamic viscosity at 40° C. is less than 3 mm2/s. Such a lubricant base oil may include a base oil (A) having % Cp of 60 or more and a kinematic viscosity at 40° C. of less than 3 mm2/s, the base oil (A) being 80% by mass or more of the total lubricant base oil mass. Such a lubricant base oil may further include a base oil (B) that is different from the base oil (A), in a range of from 1 to 20% by mass of the total lubricant base oil mass. The base oil (A) may be an isoparaffin-based base oil. Such a lubricant base oil may have a % CN of 21 or less. A cooling lubricant composition may include such a lubricant base oil.

IPC Classes  ?

• C10M 101/02 - Petroleum fractions
• C10N 20/02 - ViscosityViscosity index
• C10N 30/02 - Pour-pointViscosity index
• C10N 40/25 - Internal-combustion engines

Abstract

An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13. An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13.

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• 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 405/14 - 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 three or more hetero rings
• C07D 409/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
• C07D 409/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 50/16 - Electron transporting layers
• H10K 50/17 - Carrier injection layers
• H10K 50/18 - Carrier blocking layers
• H10K 101/10 - Triplet emission
• H10K 101/30 - Highest occupied molecular orbital [HOMO], lowest unoccupied molecular orbital [LUMO] or Fermi energy values
• H10K 101/40 - Interrelation of parameters between multiple constituent active layers or sublayers, e.g. HOMO values in adjacent layers
• H10K 102/00 - Constructional details relating to the organic devices covered by this subclass
• H10K 102/10 - Transparent electrodes, e.g. using graphene

Abstract

Provided is a polycarbonate-polyarylate resin including at least one of structural units represented by general formulae (A1) and (A2), a structural unit represented by general formula (B1), and a structural unit represented by general formula (C1), the polycarbonate-polyarylate resin being such that the molar fraction ax of structural units represented by general formula (A1), the molar fraction ay of structural units represented by general formula (A2), and the molar fraction c of structural units represented by general formula (C1) satisfy the following mathematical formula (formula 1).　(Formula 1) 0.1 ≤ {(ax_ay)/(ax+ay+c)} ×100 < 50

IPC Classes  ?

• C08G 63/64 - Polyesters containing both carboxylic ester groups and carbonate groups
• C08L 67/00 - Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chainCompositions of derivatives of such polymers
• C08L 69/00 - Compositions of polycarbonatesCompositions of derivatives of polycarbonates
• G03G 5/05 - Organic bonding materialsMethods for coating a substrate with a photoconductive layerInert supplements for use in photoconductive layers
• G03G 5/147 - Cover layers

Abstract

12312344 each independently represent a substituted or unsubstituted aromatic hydrocarbon ring having 6-50 ring-forming carbon atoms, or the like.

IPC Classes  ?

• C07D 403/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing three or more hetero rings
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/20 - Delayed fluorescence emission

Abstract

A water-soluble metalworking fluid that includes a base oil (A) and an ether carboxylic acid (B) represented by general formula (b-1), where A is a C1-4 alkylene group, when multiple A are present, each A may be the same group or may be a different group, B is a single bond or a C1-4 alkylene group, n is an integer of 1-100, and R is a hydrocarbon group. The ether carboxylic acid (B) content is 0.1-10 mass % based on the total amount of the water-soluble metalworking fluid. A water-soluble metalworking fluid that includes a base oil (A) and an ether carboxylic acid (B) represented by general formula (b-1), where A is a C1-4 alkylene group, when multiple A are present, each A may be the same group or may be a different group, B is a single bond or a C1-4 alkylene group, n is an integer of 1-100, and R is a hydrocarbon group. The ether carboxylic acid (B) content is 0.1-10 mass % based on the total amount of the water-soluble metalworking fluid.

IPC Classes  ?

• C10M 145/28 - Polyoxyalkylenes of alkylene oxides containing 2 carbon atoms only
• C10M 107/02 - Hydrocarbon polymersHydrocarbon polymers modified by oxidation
• C10M 169/04 - Mixtures of base-materials and additives
• C10N 40/22 - Metal working with essential removal of material

Abstract

A compound may include partial structures of formula (3-11B) and (31a) in one molecule: A compound may include partial structures of formula (3-11B) and (31a) in one molecule: A compound may include partial structures of formula (3-11B) and (31a) in one molecule: R314 being a single bond bonded to * in formula (31a), R300 being independently H or a substituent, or at least one of adjacent pairs of R300 are mutually bonded to form a ring, or R300 is a single bond bonded to another atom/structure in the molecule, one or more R300 is H, at least one of H being D, Y12 to Y16 being independently N, CR31, or C bonded to another atom/structure in the molecule, 1 to 3 of Y12 to Y16 being N, and R31 independently being H or a substituent.

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07D 209/86 - CarbazolesHydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
• 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 405/14 - 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 three or more hetero rings
• C07D 491/048 - Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
• C07D 495/04 - Ortho-condensed systems
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers

Abstract

An organic electroluminescence device including: a cathode, an anode, and an organic layer disposed between the cathode and the anode, wherein the organic layer comprises an emitting layer and a first layer, the first layer is disposed between the cathode and the emitting layer, the emitting layer comprises one or both of a compound represented by the following formula (1A) and a compound represented by the following formula (1B), and the first layer comprises a compound represented by the following formula (BE1): An organic electroluminescence device including: a cathode, an anode, and an organic layer disposed between the cathode and the anode, wherein the organic layer comprises an emitting layer and a first layer, the first layer is disposed between the cathode and the emitting layer, the emitting layer comprises one or both of a compound represented by the following formula (1A) and a compound represented by the following formula (1B), and the first layer comprises a compound represented by the following formula (BE1):

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 101/10 - Triplet emission

Abstract

This information processing device (PC 100) is capable of outputting information relating to a key management method for a vehicle key of a vehicle that is rented out in a vehicle rental business, said information processing device comprising: an input means 11 for inputting information relating to the vehicle (specific information that can identify the movement mode of the vehicle); a calculation means 13 for calculating respective costs of a plurality of key management methods (on-vehicle device type, locker type, etc.) on the basis of the information relating to the vehicle; and an output means 14 for outputting, on the basis of the calculation results of the calculation means 13, information about a key management method to be selected. As the respective costs, the calculation means 13 calculates the results of calculation, for each of the plurality of key management methods, of the subtraction result (net cost) obtained by subtracting an information value (for example, an advertisement fee) calculated for a case where one key management method is used, from a cost (gross cost) calculated for the case where said key management method is used.

IPC Classes  ?

• G06Q 50/10 - Services

Abstract

Provided is a zipper tape comprising a first base part and a first engagement part formed on the first base part, wherein: the first base part is folded back or can be folded back on a first side in the width direction of the zipper tape; and the first engagement part is formed on a surface which serves as an outer side when the first base part is folded back.

IPC Classes  ?

• A44B 19/16 - Interlocking member having uniform section throughout the length of the stringer
• B65D 33/00 - Details of, or accessories for, sacks or bags
• B65D 33/25 - RivetingDovetailingScrewingEnd- or aperture-closing arrangements or devices using press buttons or slide fasteners
• B65D 75/66 - Inserted or applied tearing-strings or like flexible elements

Abstract

A chalcogenide perovskite, having a crystallite size T1 of less than 40 nm, calculated by Scherrer equation based on the diffraction peak having the largest peak height in the X-ray diffraction spectrum obtained by X-ray diffraction measurement, and a proportion of a total area occupied by particles having a particle diameter of 10 μm or more measured by microscopy to a total area occupied by particles existing in a captured image range in an image range captured by a microscope of 10% or less.

IPC Classes  ?

• C09K 11/67 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing refractory metals
• C08K 9/04 - Ingredients treated with organic substances
• C09D 5/22 - Luminous paints
• C09D 7/62 - Additives non-macromolecular inorganic modified by treatment with other compounds
• C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor

Abstract

Compounds represented by formula (1).

IPC Classes  ?

• C07D 235/08 - Radicals containing only hydrogen and carbon atoms
• C07D 401/10 - 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 linked by a carbon chain containing aromatic rings
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

Disclosed is a grease composition which contains a base oil (A) and a thickening agent (B), wherein: the base oil (A) includes one or more components selected from the group consisting of the component (A1) and the component (A2) described below; and the thickening agent (B) includes one or more components selected from the group consisting of the component (B1) and the component (B2) described below. Component (A1): an ester of a polyol (A11) having 3 to 6 hydroxyl groups and a branched fatty acid (A12) having 14 to 20 carbon atoms Component (A2): an alkylnaphthalene that has a 3% mass loss temperature of 450°C or higher in gas chromatography distillation in accordance with ASTM-D7500 Component (B1): melamine cyanurate Component (B2): pre-made urea

IPC Classes  ?

• C10M 169/02 - Mixtures of base-materials and thickeners
• C10M 105/06 - Well-defined hydrocarbons aromatic
• C10M 105/38 - Esters of polyhydroxy compounds
• C10M 115/08 - Lubricating compositions characterised by the thickener being a non-macromolecular organic compound other than a carboxylic acid or salt thereof containing nitrogen
• C10N 30/06 - OilinessFilm-strengthAnti-wearResistance to extreme pressure
• C10N 30/08 - Resistance to extreme temperature
• C10N 40/00 - Specified use or application for which the lubricating composition is intended
• C10N 40/02 - Bearings
• C10N 40/04 - Oil-bathGear-boxesAutomatic transmissionsTraction drives
• C10N 50/10 - Form in which the lubricant is applied to the material being lubricated semi-solidForm in which the lubricant is applied to the material being lubricated greasy
• C10N 70/00 - Special methods of preparation

Abstract

A problem to be solved is to provide a refrigerator oil composition that has an appropriate dissolution viscosity in the case where a hydrocarbon based refrigerant is dissolved therein, and has a low solubility of a hydrocarbon based refrigerant, and a mixed composition for a refrigerator containing the refrigerator oil composition. The problem is solved by a refrigerator oil composition that is used with a refrigerant containing a hydrocarbon based refrigerant, the refrigerator oil composition containing one or more kind selected from a polyalkylene glycol based compound (A) having a number average molecular weight of 1,100 or more represented by the following general formula (1): A problem to be solved is to provide a refrigerator oil composition that has an appropriate dissolution viscosity in the case where a hydrocarbon based refrigerant is dissolved therein, and has a low solubility of a hydrocarbon based refrigerant, and a mixed composition for a refrigerator containing the refrigerator oil composition. The problem is solved by a refrigerator oil composition that is used with a refrigerant containing a hydrocarbon based refrigerant, the refrigerator oil composition containing one or more kind selected from a polyalkylene glycol based compound (A) having a number average molecular weight of 1,100 or more represented by the following general formula (1): A problem to be solved is to provide a refrigerator oil composition that has an appropriate dissolution viscosity in the case where a hydrocarbon based refrigerant is dissolved therein, and has a low solubility of a hydrocarbon based refrigerant, and a mixed composition for a refrigerator containing the refrigerator oil composition. The problem is solved by a refrigerator oil composition that is used with a refrigerant containing a hydrocarbon based refrigerant, the refrigerator oil composition containing one or more kind selected from a polyalkylene glycol based compound (A) having a number average molecular weight of 1,100 or more represented by the following general formula (1): wherein in the general formula (1), one of R1 and R2 represents a hydrogen atom, and the other thereof represents a linear or branched alkyl group having 1 or more and 16 or less carbon atoms, E represents an ethylene group, P represents a propylene group, and m and n each represent a number of 0 or more, provided that m+n is 1 or more and 50 or less.

IPC Classes  ?

• C10M 107/34 - Polyoxyalkylenes
• C08G 65/26 - Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
• C09K 5/04 - Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice-versa
• C10N 20/04 - Molecular weightMolecular weight distribution
• C10N 40/30 - Refrigerator lubricant

Abstract

A zipper tape is provided including: a first base; a male engagement portion protruding from the first base; a second base; and a female engagement portion protruding from the second base, in which the male engagement portion includes first and second hooks protruding outward, the female engagement portion includes third and fourth hooks protruding inward, the first hook is engaged with the third hook and the second hook is engaged with the fourth hook when the male engagement portion fits inside the female engagement portion, and a force required for causing the male engagement portion to fit inside the female engagement portion is in a range from 30 N/15 mm to 100 N/15 mm.

IPC Classes  ?

• B65D 33/25 - RivetingDovetailingScrewingEnd- or aperture-closing arrangements or devices using press buttons or slide fasteners

Abstract

Provided is a compound represented by formula (A), (B), (C) or (D). (Symbols in the formulas are as defined in the Description.) Also provided are: an organic electroluminescent element comprising the compound; and an electronic device comprising the organic electroluminescent element.

IPC Classes  ?

• C07C 211/58 - NaphthylaminesN-substituted derivatives thereof
• C07C 211/54 - Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to two or three six-membered aromatic rings
• C07C 211/57 - Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
• C07C 211/61 - Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton with at least one of the condensed ring systems formed by three or more rings
• C07D 209/86 - CarbazolesHydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
• C07D 307/77 - Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
• C07D 307/91 - DibenzofuransHydrogenated dibenzofurans
• C07D 405/12 - 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 chain containing hetero atoms as chain links
• C07D 405/14 - 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 three or more hetero rings
• C07D 409/12 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
• C07D 409/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 50/17 - Carrier injection layers
• H10K 50/18 - Carrier blocking layers
• H10K 59/10 - OLED displays
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/10 - Triplet emission

Abstract

An oxide semiconductor film having crystallinity over a substrate contains indium (In) and a first metal element (M1). The oxide semiconductor film includes a plurality of crystal grains. Each of the plurality of crystal grains includes at least one of a crystal orientation <001>, a crystal orientation <101>, and a crystal orientation <111> obtained by an electron backscatter diffraction (EBSD) method. In occupancy rates of crystal orientations calculated based on measurement points having crystal orientations with a crystal orientation difference greater than or equal to 0 degrees and less than or equal to 15 degrees with respect to a normal direction of a surface of the substrate, an occupancy rate of the crystal orientation <111> is greater than an occupancy rate of the crystal orientation <001> and an occupancy rate of the crystal orientation <101>.

IPC Classes  ?

• H01L 29/786 - Thin-film transistors
• C01G 15/00 - Compounds of gallium, indium, or thallium
• C23C 14/08 - Oxides
• H01L 29/66 - Types of semiconductor device

Abstract

Provided is a photoelectric conversion module capable of connecting photoelectric conversion elements with stable connection strength. The photoelectric conversion module (100) comprises a first photoelectric conversion element (10a), a second photoelectric conversion element (10b) and a connector (200). The first photoelectric conversion element (10a) and the second photoelectric conversion element (10b) are arranged side by side so as to partially overlap each other. The connector (200) is connected to the first photoelectric conversion element (10a) at a first connection portion (210). The connector (200) is connected to the second photoelectric conversion element (10b) at a second connection portion (10b) away from the first connection portion (10a).

IPC Classes  ?

• B64G 1/44 - Arrangements or adaptations of power supply systems using radiation, e.g. deployable solar arrays
• H01L 31/043 - Mechanically stacked PV cells
• H01L 31/05 - Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells
• H01L 31/18 - Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof

Abstract

11411411111 represents a heterocyclic group, the ring of that heterocyclic group do not include a nitrogen atom or a sulfur atom.

IPC Classes  ?

• C07C 15/20 - Polycyclic condensed hydrocarbons
• C07D 307/77 - Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 59/32 - Stacked devices having two or more layers, each emitting at different wavelengths
• H10K 59/95 - Assemblies of multiple devices comprising at least one organic light-emitting element wherein all light-emitting elements are organic, e.g. assembled OLED displays
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/40 - Interrelation of parameters between multiple constituent active layers or sublayers, e.g. HOMO values in adjacent layers

Abstract

111212 are each independently a group represented by general formula (11), (12), or (13), R is a hydrogen atom or a substituent of an aryl group or same, k is 1, 2, or 3, m is 0, 1, or 2, n is 1, 2, or 3, and k + m + n is 4.

IPC Classes  ?

• C07D 495/22 - Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
• C07D 209/86 - CarbazolesHydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
• C07D 251/24 - Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
• C07D 403/10 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings
• C07D 491/048 - Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 59/00 - Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

Provided is a method for producing calcium carbonate particles, whereby calcium carbonate particles having high whiteness (high purity) can be produced in a few steps.　Specifically, the method for producing calcium carbonate particles comprises mixing a Ca-containing waste, a carbonate ion-containing compound, and an organic acid.

IPC Classes  ?

• C01F 11/18 - Carbonates
• B09B 3/70 - Chemical treatment, e.g. pH adjustment or oxidation
• B09B 101/30 - Incineration ashes
• B09B 101/45 - Concrete
• B09B 101/55 - Slag

Abstract

A thin film transistor includes a metal oxide layer over the substrate, an oxide semiconductor layer having crystallinity in contact with the metal oxide layer, a gate electrode overlapping the oxide semiconductor layer, and an insulating layer between the oxide semiconductor layer and the gate electrode. The oxide semiconductor layer includes a plurality of crystal grains. Each of the plurality of crystal grains includes at least one of a crystal orientation <001>, a crystal orientation <101>, and a crystal orientation <111> obtained by an EBSD method. In occupancy rates of crystal orientations calculated based on measurement points having crystal orientations with a crystal orientation difference greater than or equal to 0 degrees and less than or equal to 15 degrees with respect to a normal direction of a surface of the substrate, an occupancy rate of the crystal orientation <001> is less than or equal to 5%.

IPC Classes  ?

• H01L 29/786 - Thin-film transistors
• H01L 29/66 - Types of semiconductor device

Abstract

Provided is a method for producing calcium carbonate particles with which it is possible to continuously produce calcium carbonate particles of high whiteness (high purity) in few steps.　Specifically, the method for producing calcium carbonate particles uses a reaction vessel 10 that is provided with a filter medium 2 compatible with crossflow filtration and is capable of circulating a suspension and circulates a suspension containing Ca-containing waste and carbonate ion-containing aqueous solution through the filter medium 2.

IPC Classes  ?

• C01F 11/18 - Carbonates
• B09B 3/70 - Chemical treatment, e.g. pH adjustment or oxidation
• B09B 101/30 - Incineration ashes
• B09B 101/45 - Concrete
• B09B 101/55 - Slag

Goods & Services

Coolants; dielectric fluids as a chemical preparation for cooling computer servers, except oils. Cooling lubricants; dielectric oils for cooling computer servers.

Abstract

There has been a need for development of a lubricating oil composition which is reduced in the oil evaporation amount at lower temperatures, and is capable of improving the fuel consumption saving.　Disclosed is a lubricating oil composition which includes a base oil (A) in which the content of a fraction containing hydrocarbon groups having not less than 14 but less than 16 carbon atoms is within the range of 0.10% by mass to 0.60% by mass based on the total amount of the base oil (A), and the content of a fraction containing hydrocarbon groups having not less than 16 but less than 18 carbon atoms is within the range of 0.35% by mass to 1.85% by mass based on the total amount of the base oil (A).

IPC Classes  ?

• C10M 171/00 - Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well defined but for which the chemical nature is either unspecified or only very vaguely indicated
• C10M 105/32 - Esters
• C10M 107/02 - Hydrocarbon polymersHydrocarbon polymers modified by oxidation
• C10N 10/12 - Groups 6 or 16
• C10N 30/00 - Specified physical or chemical property which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
• C10N 40/25 - Internal-combustion engines

Abstract

The present invention relates to a compound represented by formula (1) or formula (2).

IPC Classes  ?

• C07D 307/91 - DibenzofuransHydrogenated dibenzofurans
• C07D 209/88 - CarbazolesHydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
• 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 251/24 - Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

Disclosed is a compound which has a structure represented by general formula (1). In the general formula (1), R101to R121are each independently a hydrogen atom or a substituent, provided that at least one of R101to R111and R115to R118 is a substituted or unsubstituted N-carbazolyl group.

IPC Classes  ?

• C07F 5/02 - Boron compounds
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/20 - Delayed fluorescence emission

Abstract

A lubricant base oil having a natural origin content (ISO 16128) of 100%, may contain a monoester compound having one or more branched structures and 18 or more carbon atoms. The monoester compound may a compound of formula (1): A lubricant base oil having a natural origin content (ISO 16128) of 100%, may contain a monoester compound having one or more branched structures and 18 or more carbon atoms. The monoester compound may a compound of formula (1): A lubricant base oil having a natural origin content (ISO 16128) of 100%, may contain a monoester compound having one or more branched structures and 18 or more carbon atoms. The monoester compound may a compound of formula (1): wherein R1 and R2 are each independently a hydrocarbon group, at least one of R1 and R2 is a branched hydrocarbon group, and a total number of carbon atoms of R1 and R2 is 17 or more. In the compound of formula (1), R1 may be an alkyl group or alkenyl group having 8 or more carbon atoms, R2 may be an alkyl group or alkenyl group having 5 or more carbon atoms, and at least one of R1 and R2 may be a branched alkyl group or a branched alkenyl group

IPC Classes  ?

• C10M 105/34 - Esters of monocarboxylic acids
• C07C 53/126 - Acids containing more than four carbon atoms
• C10N 20/00 - Specified physical properties of component of lubricating compositions
• C10N 20/02 - ViscosityViscosity index

Abstract

Provided is a zipper tape-equipped container including: a container body; and a zipper tape including a first base part and a second base part attached to the container body, and a first engagement part and a second engagement part which are respectively formed on the first base part and the second base part and can engage with each other. A first engagement strength between the first engagement part and the second engagement part in a first section which is a part of 40% or less of an effective section in a length direction of the zipper tape is lower than a second engagement strength between the first engagement part and the second engagement part in a second section which is the remaining part of the effective section.

IPC Classes  ?

• B65D 33/25 - RivetingDovetailingScrewingEnd- or aperture-closing arrangements or devices using press buttons or slide fasteners
• A44B 19/16 - Interlocking member having uniform section throughout the length of the stringer
• B31B 70/81 - Forming or attaching accessories, e.g. opening devices, closures or tear strings
• B31B 160/20 - Shape of flexible containers with structural provision for thickness of contents

Abstract

An organic EL device includes an emitting region provided between a cathode and an anode, a first anode-side-organic layer, a second anode-side-organic layer, and a third anode-side-organic layer, a first emitting layer of the emitting region contains a first host material, a first additional host material, and a first luminescent compound, the first anode-side-organic layer is in direct contact with the second one, the second anode-side-organic layer is in direct contact with the third one, the third anode-side-organic layer has a film thickness of 20 nm or more, the second anode-side-organic layer contains at least one compound different from a compound contained in the third one, the first emitting layer is a fluorescent emitting layer, and a refractive index NM2 of a constituent material contained in the second anode-side-organic layer and a refractive index NM3 in the third one satisfy a relationship below, An organic EL device includes an emitting region provided between a cathode and an anode, a first anode-side-organic layer, a second anode-side-organic layer, and a third anode-side-organic layer, a first emitting layer of the emitting region contains a first host material, a first additional host material, and a first luminescent compound, the first anode-side-organic layer is in direct contact with the second one, the second anode-side-organic layer is in direct contact with the third one, the third anode-side-organic layer has a film thickness of 20 nm or more, the second anode-side-organic layer contains at least one compound different from a compound contained in the third one, the first emitting layer is a fluorescent emitting layer, and a refractive index NM2 of a constituent material contained in the second anode-side-organic layer and a refractive index NM3 in the third one satisfy a relationship below, NM 2 > NM 3 . ( Numerical ⁢ Formula ⁢ NM )

IPC Classes  ?

• H10K 50/15 - Hole transporting layers
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 50/16 - Electron transporting layers
• H10K 59/90 - Assemblies of multiple devices comprising at least one organic light-emitting element
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

A compound represented by a formula (1). A compound represented by a formula (1). A compound represented by a formula (1). In the formula (1): a ring A1, a ring B1, a ring C1, and a ring D1 are each independently a substituted or unsubstituted ring; Za, Zb, Zc, and Zd are each independently a nitrogen atom or a carbon atom; the ring C1 and the ring D1 are mutually bonded to form a ring or not mutually bonded; R1 is a hydrogen atom, substituent, or the like; R1 is mutually bonded to the ring A1 to form a ring or not mutually bonded; R1 is mutually bonded to the ring B1 to form a ring or not mutually bonded; and at least one of R1, the ring A1, the ring B1, the ring C1, or the ring D1 has a group represented by —N(R1A)(R2A).

IPC Classes  ?

• C07F 5/02 - Boron compounds
• C07B 59/00 - Introduction of isotopes of elements into organic compounds
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 85/20 - Carbon compounds, e.g. carbon nanotubes or fullerenes
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

The present application relates to an aromatic polycarbonate-based resin, including a repeating unit represented by the following formula (II): The present application relates to an aromatic polycarbonate-based resin, including a repeating unit represented by the following formula (II): The present application relates to an aromatic polycarbonate-based resin, including a repeating unit represented by the following formula (II): wherein in the formula (II), R11, R12, R13, “c”, “d”, and “n” are as defined above.

IPC Classes  ?

• C08G 64/06 - Aromatic polycarbonates not containing aliphatic unsaturation
• 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
• C08G 64/24 - General preparatory processes using carbonyl halides and phenols
• C08G 64/30 - General preparatory processes using carbonates

Abstract

A compound represented by the following formula (1): in which N*, R1 to R9, L1, L2, L3, Ar1 and Ar2 are as defined in the disclosure. An organic electroluminescent device, including a cathode, an anode, and one or more organic layers intervening between the cathode and the anode, where the one or more organic layers includes a light emitting layer, and at least one layer of the one or more organic layers contains the compound. An electronic device including the organic electroluminescent device. A compound represented by the following formula (1): in which N*, R1 to R9, L1, L2, L3, Ar1 and Ar2 are as defined in the disclosure. An organic electroluminescent device, including a cathode, an anode, and one or more organic layers intervening between the cathode and the anode, where the one or more organic layers includes a light emitting layer, and at least one layer of the one or more organic layers contains the compound. An electronic device including the organic electroluminescent device.

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• H10K 50/15 - Hole transporting layers

Abstract

33 3-is observed at 39.6±5.0 ppm in solid 313+2z1-xx4+z4+z)+(y)LiX (in the composition formula, x, y, and z satisfy 0.00060≤x≤0.15, 3.0≤y<25.0, and -0.17≤z≤1.5, respectively, and X represents a halogen atom).

IPC Classes  ?

• H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
• C03C 10/16 - Halogen-containing crystalline phase
• H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
• H01B 1/08 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances oxides
• H01M 10/0562 - Solid materials

Abstract

The present invention provides a compound that further improves the performance of an organic EL element, an organic electroluminescent element that has further improved element performance, and an electronic device that includes such an organic electroluminescent element. Provided are: a compound a represented by formula (1) [in formula (1), X1, X2, X3, U, V, W, R1-R5, R6-R9, R10-R12, R13-R15, R16-R18, R19-R23, R24-R26, and R27-R30 are as defined in the specification]; an organic electroluminescent element that contains said compound; and an electronic device that includes such an organic electroluminescent element.

IPC Classes  ?

• C07C 211/61 - Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton with at least one of the condensed ring systems formed by three or more rings
• C07D 333/76 - Dibenzothiophenes
• C07D 409/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 59/10 - OLED displays
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

Provided is a water-soluble metalworking oil agent which contains a fatty acid (B) and two or more amine compounds (A) having a volatilization rate of 20% or less as calculated from formula (i) when being heated at 50°C for 48 hours, and in which the contained amount of an amine compound (X) that does not correspond to component (A) is less than 5.0 parts by mass with respect to 100 parts by mass of the total amount of component (A). • Formula (i): Volatilization rate (%) = ([mass of amine compounds before being heated]-[mass of amine compounds after being heated for 48 hours]) / [mass of amine compounds before being heated] × 100

IPC Classes  ?

• C10M 173/00 - Lubricating compositions containing more than 10% water
• C10M 133/04 - Amines, e.g. polyalkylene polyaminesQuaternary amines
• C10M 145/26 - Polyoxyalkylenes
• C10N 30/08 - Resistance to extreme temperature
• C10N 30/16 - AntisepticBiocidal
• C10N 40/22 - Metal working with essential removal of material

Abstract

An organic EL device includes an emitting region between a cathode and an anode, a first anode side organic layer, and a second anode side organic layer, in which the emitting region includes at least a first emitting layer, the first emitting layer contains a first host material, a first additional host material, and a first luminescent compound, the first anode side organic layer contains first and second organic materials, a content of the first organic material is less than 50 mass %, the second anode side organic layer contains a second hole transporting zone material, the first emitting layer is an emitting layer that emits fluorescence, and a refractive index NM1 of constituent materials in the first anode side organic layer and a refractive index NM2 of a constituent material in the second anode side organic layer satisfy a relationship of Numerical Formula NM, An organic EL device includes an emitting region between a cathode and an anode, a first anode side organic layer, and a second anode side organic layer, in which the emitting region includes at least a first emitting layer, the first emitting layer contains a first host material, a first additional host material, and a first luminescent compound, the first anode side organic layer contains first and second organic materials, a content of the first organic material is less than 50 mass %, the second anode side organic layer contains a second hole transporting zone material, the first emitting layer is an emitting layer that emits fluorescence, and a refractive index NM1 of constituent materials in the first anode side organic layer and a refractive index NM2 of a constituent material in the second anode side organic layer satisfy a relationship of Numerical Formula NM, NM 1 > NM 2 . ( Numerical ⁢ Formula ⁢ NM )

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/15 - Hole transporting layers
• H10K 101/00 - Properties of the organic materials covered by group

Abstract

An organic solid up-conversion material contains a triplet sensitizer and an organic luminescent material. The triplet sensitizer and the organic luminescent material satisfy relations of a numerical formula (Numerical Formula 1) and a numerical formula (Numerical Formula 2), and the triplet sensitizer and the organic luminescent material form a solid solution crystal. An organic solid up-conversion material contains a triplet sensitizer and an organic luminescent material. The triplet sensitizer and the organic luminescent material satisfy relations of a numerical formula (Numerical Formula 1) and a numerical formula (Numerical Formula 2), and the triplet sensitizer and the organic luminescent material form a solid solution crystal. T1(M1)≥T1(M2)  (Numerical Formula 1) An organic solid up-conversion material contains a triplet sensitizer and an organic luminescent material. The triplet sensitizer and the organic luminescent material satisfy relations of a numerical formula (Numerical Formula 1) and a numerical formula (Numerical Formula 2), and the triplet sensitizer and the organic luminescent material form a solid solution crystal. T1(M1)≥T1(M2)  (Numerical Formula 1) S1(M2)>S1(M1)  (Numerical Formula 2) An organic solid up-conversion material contains a triplet sensitizer and an organic luminescent material. The triplet sensitizer and the organic luminescent material satisfy relations of a numerical formula (Numerical Formula 1) and a numerical formula (Numerical Formula 2), and the triplet sensitizer and the organic luminescent material form a solid solution crystal. T1(M1)≥T1(M2)  (Numerical Formula 1) S1(M2)>S1(M1)  (Numerical Formula 2) (S1(M1) is the lowest singlet energy of the triplet sensitizer, T1(M1) is the lowest triplet energy of the triplet sensitizer, S1(M2) is the lowest singlet energy of the organic luminescent material, and T1(M2) is the lowest triplet energy of the organic luminescent material.)

IPC Classes  ?

• C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials

Abstract

3+2z1-xx4+z4+z)+(y)LiX (wherein x, y, and z respectively satisfy 0.00060≤x≤0.25, 0.50≤y≤14.0, and -0.17≤z≤1.5 and X represents a halogen atom).

IPC Classes  ?

• H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
• C03C 10/16 - Halogen-containing crystalline phase
• H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
• H01B 1/08 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances oxides
• H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
• H01M 10/052 - Li-accumulators
• H01M 10/0562 - Solid materials

Abstract

An organic electroluminescence device includes an emitting region provided between an anode and a cathode, in which the emitting region includes a first emitting layer and a second emitting layer, a ratio DEM1/DEM2 of a film thickness DEM1 of the first emitting layer to a film thickness DEM2 of the second emitting layer is in a range from 2/3 to 3/2, the first emitting layer contains a first host material and a first luminescent compound, the second emitting layer contains a second host material and a second luminescent compound, and the first host material is a compound represented by a formula (1) below having a group represented by a formula (10). An organic electroluminescence device includes an emitting region provided between an anode and a cathode, in which the emitting region includes a first emitting layer and a second emitting layer, a ratio DEM1/DEM2 of a film thickness DEM1 of the first emitting layer to a film thickness DEM2 of the second emitting layer is in a range from 2/3 to 3/2, the first emitting layer contains a first host material and a first luminescent compound, the second emitting layer contains a second host material and a second luminescent compound, and the first host material is a compound represented by a formula (1) below having a group represented by a formula (10).

IPC Classes  ?

• G06K 1/12 - Methods or arrangements for marking the record carrier in digital fashion otherwise than by punching

Abstract

Provided is a photoelectric conversion module capable of improving bonding strength between photoelectric conversion elements adjacent to each other. The photoelectric conversion module (100) comprises a first photoelectric conversion element (10a) including a collector electrode (30a) and a second photoelectric conversion element (10b) including a conductive substrate (20b). The first photoelectric conversion element (10a) and the second photoelectric conversion element (10b) are arranged side by side so as to partially overlap each other. The photoelectric conversion module comprises a conductor (200) electrically connecting the collector electrode (30a) of the first photoelectric conversion element (10a) and the conductive substrate (20b) of the second photoelectric conversion element (10b) to each other. The conductor (200) is provided from a region of the collector electrode (30a) of the first photoelectric conversion element (10a) to a region outside the collector electrode (30a).

IPC Classes  ?

• H01L 31/05 - Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells
• B64G 1/44 - Arrangements or adaptations of power supply systems using radiation, e.g. deployable solar arrays
• H01L 31/0392 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by their semiconductor bodies characterised by their crystalline structure or particular orientation of the crystalline planes including thin films deposited on metallic or insulating substrates
• H01L 31/18 - Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof

Abstract

A server for enabling automatic determination of the lending type for a vehicle returned from a user in a vehicle lending service for lending out a vehicle to the user includes first calculation means for calculating, based on information (revenues and expenses) corresponding to a state value of a battery, a subscription profit to be gained when the returned vehicle is lent out for subscription and a share profit to be gained when the returned vehicle is lent out for car share. The server also includes determination means for determining the subscription or the car share as the lending type for the returned vehicle based on the subscription profit and the share profit that have been calculated.

IPC Classes  ?

• G06Q 50/40 - Business processes related to the transportation industry
• G06Q 40/12 - Accounting

Abstract

A compound is represented by a formula (1) below, in which k is an integer of 0 or more, m is an integer of 1 or more, n is an integer of 2 or more. L is a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, CN is a cyano group, and D1 and D2 are each independently represented by one of a formula (2), a formula (3) and formula (3x) below, D1 and D2 being optionally mutually the same or different. A compound is represented by a formula (1) below, in which k is an integer of 0 or more, m is an integer of 1 or more, n is an integer of 2 or more. L is a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, CN is a cyano group, and D1 and D2 are each independently represented by one of a formula (2), a formula (3) and formula (3x) below, D1 and D2 being optionally mutually the same or different.

IPC Classes  ?

• C07D 209/80 - [b, c]- or [b, d]-condensed
• C07D 209/82 - CarbazolesHydrogenated carbazoles
• C07D 209/94 - [b, c]- or [b, d]-condensed containing carbocyclic rings other than six-membered
• C07D 491/048 - Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
• C07D 491/147 - Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

112112122 each independently represent an oxygen atom or a sulfur atom.

IPC Classes  ?

• C07D 493/04 - Ortho-condensed systems
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• H10K 50/13 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light comprising stacked EL layers within one EL unit
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/40 - Interrelation of parameters between multiple constituent active layers or sublayers, e.g. HOMO values in adjacent layers

Abstract

The compound is represented by formula (1).

IPC Classes  ?

• C07D 235/26 - Oxygen atoms
• H10K 50/00 - Organic light-emitting devices
• H10K 50/10 - OLEDs or polymer light-emitting diodes [PLED]
• H10K 50/15 - Hole transporting layers
• H10K 50/16 - Electron transporting layers
• H10K 59/00 - Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group
• H10K 59/10 - OLED displays
• H10K 85/60 - Organic compounds having low molecular weight

Abstract

A method for producing ammonia from nitrogen molecules with a reducing agent and a proton source, the method using, as a catalyst, a molybdenum complex obtained by reacting a ligand of Formula (1) and a molybdenum compound: A method for producing ammonia from nitrogen molecules with a reducing agent and a proton source, the method using, as a catalyst, a molybdenum complex obtained by reacting a ligand of Formula (1) and a molybdenum compound: A method for producing ammonia from nitrogen molecules with a reducing agent and a proton source, the method using, as a catalyst, a molybdenum complex obtained by reacting a ligand of Formula (1) and a molybdenum compound: wherein R1 and R2 are each independently C3-10 alkyl group, R3, R4 and R5 are each independently a hydrogen atom, a fluorine atom, a trifluoromethyl group, a phenyl group, or an Ar1 aryl group, and at least one of R3, R4 and R5 is a phenyl group or an Ar1 aryl group, a molybdenum complex used in the method and a ligand that is a raw material for the molybdenum.

IPC Classes  ?

• C01C 1/04 - Preparation of ammonia by synthesis
• B01J 31/24 - Phosphines

Abstract

Provided are a compound for further improving the capability of an organic EL device, an organic electroluminescent device having a further improved device capability, and an electronic device including such an organic electroluminescent device, in which the compound is represented by the following formula (1): [in formula (1), N*, *a1, *a3, *b1, m, n, R1A to R5A, R1B to R5B, R11B to R14B, R21A to R25A, R21B to R24B, L, Ar1, Ar2 and Ar3 are as defined in the description], the organic electroluminescent device is an organic electroluminescent device including the compound, and the electronic device is an electronic device including such an organic electroluminescent device. Provided are a compound for further improving the capability of an organic EL device, an organic electroluminescent device having a further improved device capability, and an electronic device including such an organic electroluminescent device, in which the compound is represented by the following formula (1): [in formula (1), N*, *a1, *a3, *b1, m, n, R1A to R5A, R1B to R5B, R11B to R14B, R21A to R25A, R21B to R24B, L, Ar1, Ar2 and Ar3 are as defined in the description], the organic electroluminescent device is an organic electroluminescent device including the compound, and the electronic device is an electronic device including such an organic electroluminescent device.

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07C 211/54 - Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to two or three six-membered aromatic rings
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/15 - Hole transporting layers
• H10K 102/00 - Constructional details relating to the organic devices covered by this subclass

Abstract

A mixed powder for an organic electroluminescence device, including a first organic compound and a second organic compound, and being solid at ordinary temperatures and pressures, wherein the organic electroluminescence device includes a cathode, an anode, and an emitting layer arranged between the cathode and the anode, and the emitting layer includes a compound C2 having delayed fluorescence, and each of the first organic compound and the second organic compound is a compound selected from the group consisting of a fluorescent emitting compound C1, the compound C2, and a compound C3 different from both the compound C1 and the compound C2, and they have the specific combination, wherein when MOL1 [mol %] is used as the molar concentration of the first organic compound in the mixed powder and MOL2 [mol %] is used as the molar concentration of the second organic compound in the mixed powder, MOL1 [mol %] and MOL2 [mol %] satisfy the following formula (1), wherein when M1 [kg/mol] is used as the molecular weight of the first organic compound, when P1 [Pa] is used as the vapor pressure obtained by ThermoGravimetry-Differential Thermal Analysis of the first organic compound at arbitrary temperature, when M2 [kg/mol] is used as the molecular weight of the second organic compound, and when P2 [Pa] is used as the vapor pressure obtained by ThermoGravimetry-Differential Thermal Analysis of the second organic compound at arbitrary temperature, the temperature T1 [° C.] of the first organic compound in the case of P1/M11/2=0.04×{MOL1/(MOL1+MOL2)} and the temperature T2 [° C.] of the second organic compound in the case of P2/M21/2=0.04×{MOL2/(MOL1+MOL2)} satisfy the following formula (2): A mixed powder for an organic electroluminescence device, including a first organic compound and a second organic compound, and being solid at ordinary temperatures and pressures, wherein the organic electroluminescence device includes a cathode, an anode, and an emitting layer arranged between the cathode and the anode, and the emitting layer includes a compound C2 having delayed fluorescence, and each of the first organic compound and the second organic compound is a compound selected from the group consisting of a fluorescent emitting compound C1, the compound C2, and a compound C3 different from both the compound C1 and the compound C2, and they have the specific combination, wherein when MOL1 [mol %] is used as the molar concentration of the first organic compound in the mixed powder and MOL2 [mol %] is used as the molar concentration of the second organic compound in the mixed powder, MOL1 [mol %] and MOL2 [mol %] satisfy the following formula (1), wherein when M1 [kg/mol] is used as the molecular weight of the first organic compound, when P1 [Pa] is used as the vapor pressure obtained by ThermoGravimetry-Differential Thermal Analysis of the first organic compound at arbitrary temperature, when M2 [kg/mol] is used as the molecular weight of the second organic compound, and when P2 [Pa] is used as the vapor pressure obtained by ThermoGravimetry-Differential Thermal Analysis of the second organic compound at arbitrary temperature, the temperature T1 [° C.] of the first organic compound in the case of P1/M11/2=0.04×{MOL1/(MOL1+MOL2)} and the temperature T2 [° C.] of the second organic compound in the case of P2/M21/2=0.04×{MOL2/(MOL1+MOL2)} satisfy the following formula (2): 0 < MOL ⁢ 2 / ( MOL ⁢ 1 + MOL ⁢ 2 ) ≦ 0.45 ( 1 ) - 20 ⁢ ° ⁢ C . ≦ T ⁢ 1 - T ⁢ 2 ≦ 40 ⁢ ° ⁢ C .. ( 2 )

IPC Classes  ?

• H10K 71/12 - Deposition of organic active material using liquid deposition, e.g. spin coating
• C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/20 - Delayed fluorescence emission

Abstract

An organic EL device includes a first emitting layer and a second emitting layer, in which the first emitting layer contains a first host material, the second emitting layer contains a second host material, the first emitting layer at least contains a first emitting compound that emits light having a maximum peak wavelength of 500 nm or less, the second emitting layer at least contains a second emitting compound that emits light having a maximum peak wavelength of 500 nm or less, a total of a film thickness of the first emitting layer and a film thickness of the second emitting layer is 20 nm or less, and a triplet energy of the first host material T1(H1) and a triplet energy of the second host material T1(H2) satisfy a relationship of (Numerical Formula 1): T1(H1) greater than T1(H2).

IPC Classes  ?

• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/00 - Properties of the organic materials covered by group
• H10K 101/30 - Highest occupied molecular orbital [HOMO], lowest unoccupied molecular orbital [LUMO] or Fermi energy values
• H10K 102/00 - Constructional details relating to the organic devices covered by this subclass

Abstract

A compound may have formula (1): A compound may have formula (1): A compound may have formula (1): D11 and D12 independently being a group of formula (11), (12), or (13): A compound may have formula (1): D11 and D12 independently being a group of formula (11), (12), or (13): A compound may have formula (1): D11 and D12 independently being a group of formula (11), (12), or (13): At least one D11 may be a group of formula (12) or (13). R may be, for instance, a hydrogen atom or an aryl group.

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07D 495/14 - Ortho-condensed systems
• C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 101/25 - Delayed fluorescence emission using exciplex

Abstract

A radio wave absorber having a structure in which a dielectric body and a conductor having a plurality of regularly arrayed openings have been stacked, wherein the length of the longest part of the openings is 0.1-2% of the wavelength to be absorbed.

IPC Classes  ?

• H05K 9/00 - Screening of apparatus or components against electric or magnetic fields

Abstract

Provided are: a novel compound capable of preparing a lubricating oil composition having excellent friction reduction effect and abrasion resistance; and a novel additive containing said compound.　This compound is represented by general formula (1).　

IPC Classes  ?

• C07C 69/40 - Succinic acid esters
• C07C 211/03 - Monoamines
• C07C 211/21 - Monoamines
• C07C 215/12 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic the nitrogen atom of the amino group being further bound to hydrocarbon groups substituted by hydroxy groups
• C07C 215/24 - Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and acyclic
• C10M 129/40 - Carboxylic acidsSalts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms monocarboxylic
• C10M 133/06 - Amines, e.g. polyalkylene polyaminesQuaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
• C10M 133/16 - AmidesImides
• C10M 135/22 - ThiolsSulfidesPolysulfides containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
• C10N 30/00 - Specified physical or chemical property which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
• C10N 40/04 - Oil-bathGear-boxesAutomatic transmissionsTraction drives
• C10N 40/06 - Instruments or other precision apparatus, e.g. damping fluids
• C10N 40/08 - Hydraulic fluids, e.g. brake-fluids
• C10N 40/25 - Internal-combustion engines

Abstract

A lubricating oil composition that satisfies the fuel efficiency with a low viscosity and a low traction coefficient, the wear resistance, the usability with a high flash point, and the low temperature fluidity, at high levels, having a base oil having a kinematic viscosity at 40° C. of 3.000 mm2/s or more and 20.000 mm2/s or less as a component (A); and a base oil having a kinematic viscosity at 40°° C. of 100.000 mm2/s or more and 2000.000 mm2/s or less as a component (B), the component (A) having a flash point of 180° C. or more, the lubricating oil composition having a content of the component (B) of 0.01% by mass or more and 2.00% by mass or less based on the total amount of the lubricating oil composition, a lubricating method using the same, and a transmission including the same.

IPC Classes  ?

• C10M 101/02 - Petroleum fractions
• C10M 107/02 - Hydrocarbon polymersHydrocarbon polymers modified by oxidation
• C10M 107/32 - Condensation polymers of aldehydes or ketonesPolyestersPolyethers
• C10M 137/04 - Phosphate esters
• C10N 20/02 - ViscosityViscosity index
• C10N 20/04 - Molecular weightMolecular weight distribution
• C10N 30/06 - OilinessFilm-strengthAnti-wearResistance to extreme pressure
• C10N 40/04 - Oil-bathGear-boxesAutomatic transmissionsTraction drives

Abstract

Specific compounds, a material, preferably an emitter material, may be suitable for an organic electroluminescence device, and be of formula (I): Specific compounds, a material, preferably an emitter material, may be suitable for an organic electroluminescence device, and be of formula (I): Specific compounds, a material, preferably an emitter material, may be suitable for an organic electroluminescence device, and be of formula (I): An organic electroluminescence device may include such compounds. An electronic equipment may include such an organic electroluminescence device. A light emitting layer may include at least one host and at least one dopant, the dopant including at least one of such compounds. Such compounds may be used in an organic electroluminescence device.

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07F 5/02 - Boron compounds
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants

Abstract

Provided is a highly convenient vehicle lending service. Included are first reception means (111) for receiving registration of a subscription member, second reception means (112) for receiving registration of a car share member, storage means (120) for storing registration information that sets a user as the subscription member based on the reception performed by the first reception means (111) and storing registration information that sets the user as the car share member based on the reception performed by the second reception means (112), and payment means (170) for executing payment processing for a usage fee for subscription and executing payment processing for a usage fee for car share. The storage means (120) is allowed to store, based on the reception performed by the first reception means (111), registration information that sets the user as the car share member while setting the user as the subscription member. The payment means (170) is allowed to execute lump-sum payment processing for collectively paying the usage fee for the subscription and the usage fee for the car share.

IPC Classes  ?

• G06Q 50/43 - Business processes related to the sharing of vehicles, e.g. car sharing
• G06Q 10/02 - Reservations, e.g. for tickets, services or events
• G06Q 20/22 - Payment schemes or models

Abstract

A silicon-containing alicyclic hydrocarbon-based polymer satisfies the following (1)-(5): (1) A glass transition temperature is 70-140 °C; (2) the polymer has no melting point at 50 °C or lower and no melting point at 140 °C or higher; (3) a weight average molecular weight is 5,000-150,000; (4) a molecular weight distribution (Mw/Mn) is 1.0-6.0; and (5) a silicon element is included in an amount of 0.1-2.0 mass% in terms of silicon atom.

IPC Classes  ?

• C08F 283/14 - Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass on to polymers obtained by ring-opening polymerisation of carbocyclic compounds having one or more carbon-to-carbon double bonds in the carbocyclic ring, i.e. polyalkeneamers
• C08F 8/42 - Introducing metal atoms or metal-containing groups
• C08F 277/00 - Macromolecular compounds obtained by polymerising monomers on to polymers of carbocyclic or heterocyclic monomers as defined respectively in group or in group
• C08G 61/00 - Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
• C08L 51/00 - Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers
• C08L 65/00 - Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chainCompositions of derivatives of such polymers
• C08L 95/00 - Compositions of bituminous materials, e.g. asphalt, tar or pitch

Abstract

111111(M2)

IPC Classes  ?

• H10K 50/12 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
• C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/11 - OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
• H10K 59/10 - OLED displays
• H10K 85/60 - Organic compounds having low molecular weight
• H10K 101/20 - Delayed fluorescence emission

Abstract

The present invention provides a compound that further improves the performance of an organic EL device, an organic electroluminescent device having further improved device performance, and an electronic appliance including such an organic electroluminescent device. Provided is a compound represented by the following formula (1): The present invention provides a compound that further improves the performance of an organic EL device, an organic electroluminescent device having further improved device performance, and an electronic appliance including such an organic electroluminescent device. Provided is a compound represented by the following formula (1): The present invention provides a compound that further improves the performance of an organic EL device, an organic electroluminescent device having further improved device performance, and an electronic appliance including such an organic electroluminescent device. Provided is a compound represented by the following formula (1): [In the formula (1), N*, *a1 to *a3, *b1 to *b3, *p1, m1 to m3, n1 to n3, R1A to R5A, R1B to R5B R11A to R15A, R11B to R15B, R21A to R25A, R21B to R25B, R31 to R35, R36 to R39, R40 to R43, R44 to R48, Ar1, and Ar2 are as defined in the description], an organic electroluminescent device containing the compound, and an electronic appliance including such an organic electroluminescent device.

IPC Classes  ?

• H10K 85/60 - Organic compounds having low molecular weight
• C07C 211/54 - Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to two or three six-membered aromatic rings
• C07D 307/91 - DibenzofuransHydrogenated dibenzofurans
• C09K 11/06 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing organic luminescent materials
• H10K 50/15 - Hole transporting layers
• H10K 102/00 - Constructional details relating to the organic devices covered by this subclass

Abstract

A resin composition comprising a resin(S) comprising: a polyerytene other (A) having a ratio of peak integral value of 3.80 to 3.92 ppm relative to a peak integral value of 6.20 to 6.72 ppm being 0.05 to 5.0%, in 1H-NMR spectrum obtained by 1H-NMR spectrum measurement using deuterated chloroform as a solvent, and a thermoplastic resin (B), and an inorganic filler (C).

IPC Classes  ?

• C08L 25/06 - Polystyrene
• C08K 7/06 - Elements

Abstract

Specific compounds represented by formula (I), a material for an organic electroluminescence device comprising said specific compound, an organic electroluminescence device comprising said specific compound, an electronic equipment comprising said organic electroluminescence device and the use of said compounds in an organic electroluminescence device. Specific compounds represented by formula (I), a material for an organic electroluminescence device comprising said specific compound, an organic electroluminescence device comprising said specific compound, an electronic equipment comprising said organic electroluminescence device and the use of said compounds in an organic electroluminescence device.

IPC Classes  ?

• C07D 401/10 - 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 linked by a carbon chain containing aromatic rings
• C07B 59/00 - Introduction of isotopes of elements into organic compounds
• C07D 401/14 - 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 three or more hetero rings
• C07D 405/14 - 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 three or more hetero rings
• C07D 409/14 - Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• C07D 493/04 - Ortho-condensed systems
• H10K 50/16 - Electron transporting layers
• H10K 85/60 - Organic compounds having low molecular weight