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.
C10M 129/02 - Compositions lubrifiantes caractérisées en ce que l'additif est un composé organique non macromoléculaire contenant de l'oxygène comportant une chaîne carbonée de moins de 30 atomes
C10M 159/00 - Compositions lubrifiantes caractérisées en ce que l'additif est de constitution indéterminée ou incomplètement déterminée
C10M 169/04 - Mélanges de matériaux de base et d'additifs
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.
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.
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.
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.
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01M 10/42 - Procédés ou dispositions pour assurer le fonctionnement ou l'entretien des éléments secondaires ou des demi-éléments secondaires
6.
COMPOUND, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
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).
C09K 11/02 - Emploi de substances particulières comme liants, revêtements de particules ou milieux de suspension
H10K 50/13 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] spécialement adaptées à l'émission de lumière multicolore, p. ex. à l'émission de lumière blanche comprenant des couches EL empilées dans une unité EL
7.
CRYSTALLINE SULFIDE SOLID ELECTROLYTE AND METHOD FOR MANUFACTURING SAME
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.
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 13/00 - Appareils ou procédés spécialement adaptés à la fabrication de conducteurs ou câbles
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).
C07B 59/00 - Introduction d'isotopes d'éléments dans les composés organiques
C07C 13/547 - Hydrocarbures polycycliques ou leurs dérivés hydrocarbonés acycliques à cycles condensés à trois cycles condensés un cycle au moins n'étant pas un cycle à six chaînons, les autres cycles étant au plus des cycles à six chaînons
C07C 15/38 - Hydrocarbures polycycliques condensés contenant quatre cycles
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).
C09K 5/04 - Substances qui subissent un changement d'état physique lors de leur utilisation le changement d'état se faisant par passage de l'état liquide à l'état vapeur ou vice versa
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.
C10N 30/00 - Propriétés physiques ou chimiques particulières améliorées par l'additif caractérisant la composition lubrifiante, p. ex. additifs multifonctionnels
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.
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01M 4/136 - Électrodes à base de composés inorganiques autres que les oxydes ou les hydroxydes, p. ex. sulfures, séléniures, tellurures, halogénures ou LiCoFy
H01M 4/58 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de composés inorganiques autres que les oxydes ou les hydroxydes, p. ex. sulfures, séléniures, tellurures, halogénures ou LiCoFyEmploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de structures polyanioniques, p. ex. phosphates, silicates ou borates
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p. ex. batteries à insertion ou intercalation de lithium dans les deux électrodesBatteries à l'ion lithium
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.)
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
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.
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.
H01L 29/04 - Corps semi-conducteurs caractérisés par leur structure cristalline, p.ex. polycristalline, cubique ou à orientation particulière des plans cristallins
H01L 29/06 - Corps semi-conducteurs caractérisés par les formes, les dimensions relatives, ou les dispositions des régions semi-conductrices
H01L 29/49 - Electrodes du type métal-isolant-semi-conducteur
15.
SULFIDE SOLID ELECTROLYTE MIXTURE, ELECTRODE MIXTURE, AND ALL-SOLID-STATE BATTERY
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.
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01M 4/13 - Électrodes pour accumulateurs à électrolyte non aqueux, p. ex. pour accumulateurs au lithiumLeurs procédés de fabrication
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p. ex. liants, charges
H01M 10/056 - Accumulateurs à électrolyte non aqueux caractérisés par les matériaux utilisés comme électrolytes, p. ex. électrolytes mixtes inorganiques/organiques
16.
RADIO WAVE ABSORBER, RADIO WAVE ABSORPTION STRUCTURE INCLUDING RADIO WAVE ABSORBER, AND COMPOSITION FOR RADIO WAVE ABSORBER
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.
H01Q 17/00 - Dispositifs pour absorber les ondes rayonnées par une antenneCombinaisons de tels dispositifs avec des éléments ou systèmes d'antennes actives
17.
ELECTRODE, LITHIUM ION BATTERY POSITIVE ELECTRODE, AND LITHIUM ION BATTERY
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%.
H01M 10/0585 - Structure ou fabrication d'accumulateurs ayant uniquement des éléments de structure plats, c.-à-d. des électrodes positives plates, des électrodes négatives plates et des séparateurs plats
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
04 - Huiles et graisses industrielles; lubrifiants; combustibles
Produits et services
Coolants; dielectric fluids as a chemical preparation for
cooling computer servers, except oils. Cooling lubricants; dielectric oils for cooling computer
servers.
19.
ORGANIC ELECTROLUMINESCENCE ELEMENT, ELECTRONIC DEVICE, COMPOSITION, AND MIXTURE POWDER
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
)
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 50/13 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] spécialement adaptées à l'émission de lumière multicolore, p. ex. à l'émission de lumière blanche comprenant des couches EL empilées dans une unité EL
H10K 85/60 - Composés organiques à faible poids moléculaire
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
23.
COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
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.
C10M 157/10 - Compositions lubrifiantes caractérisées en ce que l'additif est un mélange d'au moins deux composés macromoléculaires couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé contenant des atomes d'éléments non prévus par les groupes
C10N 20/04 - Poids moléculaireRépartition du poids moléculaire
C10N 30/02 - Point d'écoulementIndice de viscosité
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/08 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques oxydes
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p. ex. liants, charges
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).
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
28.
PRODUCTION METHOD FOR SULFIDE SOLID ELECTROLYTE AND SULFIDE SOLID ELECTROLYTE
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.
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.
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C07D 405/12 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 85/60 - Composés organiques à faible poids moléculaire
C07D 239/26 - Composés hétérocycliques contenant des cycles diazine-1, 3 ou diazine-1, 3 hydrogéné non condensés avec d'autres cycles comportant au moins trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du cycle
C07D 251/24 - Composés hétérocycliques contenant des cycles triazine-1, 3, 5 non condensés avec d'autres cycles comportant trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des atomes d'hydrogène ou de carbone liés directement à au moins un atome de carbone du cycle à trois atomes de carbone du cycle
C07D 403/10 - Composés hétérocycliques contenant plusieurs hétérocycles, comportant des atomes d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 405/10 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
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).
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.
C10M 111/02 - Compositions lubrifiantes caractérisées en ce que le matériau de base est un mélange d'au moins deux composés couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé organique non macromoléculaire
C10M 133/40 - Cycle à six chaînons ne contenant que du carbone et de l'azote
C10N 30/04 - Propriétés détergentes ou dispersantes
C10N 30/10 - Inhibition de l'oxydation, p. ex. anti-oxydants
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.
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.
H10K 30/40 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire comprenant une structure p-i-n, ayant p. ex. un absorbeur pérovskite entre des couches de transport de charge de type p et de type n
H10K 30/57 - Dispositifs photovoltaïques [PV] comprenant des jonctions multiples, p. ex. des cellules PV en tandem
H10K 30/86 - Couches à haute mobilité des trous, p. ex. de transport des trous ou couches de blocage des électrons
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)).
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
C08F 2/44 - Polymérisation en présence d'additifs, p. ex. plastifiants, matières colorantes, charges
C08F 20/00 - Homopolymères ou copolymères de composés contenant un ou plusieurs radicaux aliphatiques non saturés, chaque radical ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle ou un sel, anhydride, ester, amide, imide ou nitrile
C08F 292/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des substances inorganiques
C08F 293/00 - Composés macromoléculaires obtenus par polymérisation sur une macromolécule contenant des groupes capables d'amorcer la formation de nouvelles chaînes polymères rattachées exclusivement à une ou aux deux extrémités de la macromolécule de départ
C08K 3/013 - Charges, pigments ou agents de renforcement
C08K 7/00 - Emploi d'ingrédients caractérisés par leur forme
C08K 9/06 - Ingrédients traités par des substances organiques par des composés contenant du silicium
C08L 33/00 - Compositions contenant des homopolymères ou des copolymères de composés possédant un ou plusieurs radicaux aliphatiques non saturés, chacun ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle, ou ses sels, anhydrides, esters, amides, imides ou nitrilesCompositions contenant des dérivés de tels polymères
C08L 51/10 - Compositions contenant des polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères greffés sur des substances inorganiques
C08L 53/00 - Compositions contenant des copolymères séquencés possédant au moins une séquence d'un polymère obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères
37.
PHOTOELECTRIC CONVERSION ELEMENT, SOLAR CELL MODULE, AND PADDLE
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.
C25B 9/00 - Cellules ou assemblages de cellulesÉléments de structure des cellulesAssemblages d'éléments de structure, p. ex. assemblages d'électrode-diaphragmeCaractéristiques des cellules relatives aux procédés
C25B 9/21 - Cellules comprenant des électrodes fixes de dimensions stablesAssemblages de leurs éléments de structure avec des diaphragmes avec plusieurs diaphragmes
C25B 13/08 - DiaphragmesÉléments d'espacement caractérisés par le matériau à base de matériaux organiques
39.
THERMOSETTING COMPOSITION, METHOD FOR PRODUCING MOLDED ARTICLE USING SAME, AND CURED PRODUCT
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)
C08F 2/44 - Polymérisation en présence d'additifs, p. ex. plastifiants, matières colorantes, charges
C08F 20/00 - Homopolymères ou copolymères de composés contenant un ou plusieurs radicaux aliphatiques non saturés, chaque radical ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle ou un sel, anhydride, ester, amide, imide ou nitrile
C08F 287/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des polymères séquencés
C08F 292/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des substances inorganiques
C08F 293/00 - Composés macromoléculaires obtenus par polymérisation sur une macromolécule contenant des groupes capables d'amorcer la formation de nouvelles chaînes polymères rattachées exclusivement à une ou aux deux extrémités de la macromolécule de départ
C08K 3/013 - Charges, pigments ou agents de renforcement
C08K 9/06 - Ingrédients traités par des substances organiques par des composés contenant du silicium
C08L 33/00 - Compositions contenant des homopolymères ou des copolymères de composés possédant un ou plusieurs radicaux aliphatiques non saturés, chacun ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle, ou ses sels, anhydrides, esters, amides, imides ou nitrilesCompositions contenant des dérivés de tels polymères
C08L 51/10 - Compositions contenant des polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères greffés sur des substances inorganiques
C08L 53/00 - Compositions contenant des copolymères séquencés possédant au moins une séquence d'un polymère obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères
40.
THERMOSETTING COMPOSITION, METHOD FOR PRODUCING MOLDED ARTICLE USING SAME, AND CURED PRODUCT
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)
C08F 2/44 - Polymérisation en présence d'additifs, p. ex. plastifiants, matières colorantes, charges
C08F 20/00 - Homopolymères ou copolymères de composés contenant un ou plusieurs radicaux aliphatiques non saturés, chaque radical ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle ou un sel, anhydride, ester, amide, imide ou nitrile
C08F 287/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des polymères séquencés
C08F 292/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des substances inorganiques
C08F 293/00 - Composés macromoléculaires obtenus par polymérisation sur une macromolécule contenant des groupes capables d'amorcer la formation de nouvelles chaînes polymères rattachées exclusivement à une ou aux deux extrémités de la macromolécule de départ
C08K 3/013 - Charges, pigments ou agents de renforcement
C08K 9/06 - Ingrédients traités par des substances organiques par des composés contenant du silicium
C08L 33/00 - Compositions contenant des homopolymères ou des copolymères de composés possédant un ou plusieurs radicaux aliphatiques non saturés, chacun ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle, ou ses sels, anhydrides, esters, amides, imides ou nitrilesCompositions contenant des dérivés de tels polymères
C08L 51/10 - Compositions contenant des polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères greffés sur des substances inorganiques
C08L 53/00 - Compositions contenant des copolymères séquencés possédant au moins une séquence d'un polymère obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères
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.
C08J 11/12 - Récupération ou traitement des résidus des polymères par coupure des chaînes moléculaires des polymères ou rupture des liaisons de réticulation par voie chimique, p. ex. dévulcanisation uniquement par traitement à la chaleur sèche
C10B 53/07 - Distillation destructive spécialement conçue pour des matières premières solides particulières ou sous forme spéciale de matières polymères synthétiques, p. ex. pneumatiques
C10G 1/10 - Production de mélanges liquides d'hydrocarbures à partir de schiste bitumineux, de sable pétrolifère ou de matières carbonées solides non fusibles ou similaires, p. ex. bois, charbon à partir de caoutchouc ou de déchets de caoutchouc
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.
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.
H10K 85/60 - Composés organiques à faible poids moléculaire
C07D 405/10 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 405/14 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C07D 409/10 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 409/14 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C09K 11/02 - Emploi de substances particulières comme liants, revêtements de particules ou milieux de suspension
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
H10K 102/00 - Détails de structure relatifs aux dispositifs organiques couverts par la présente sous-classe
H10K 102/10 - Électrodes transparentes, p. ex. utilisant du graphène
44.
POLYCARBONATE-POLYARYLATE RESIN, COATING COMPOSITION, MOLDED BODY, AND ELECTROPHOTOGRAPHIC PHOTORECEPTOR
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
C08G 63/64 - Polyesters contenant à la fois des groupes ester carboxylique et des groupes carbonate
C08L 67/00 - Compositions contenant des polyesters obtenus par des réactions créant une liaison ester carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
C08L 69/00 - Compositions contenant des polycarbonatesCompositions contenant des dérivés des polycarbonates
G03G 5/05 - Matériaux de liaison organiquesMéthodes d'enduction d'un substrat avec une couche photoconductriceAdditifs inertes utilisables dans des couches photoconductrices
C07D 403/14 - Composés hétérocycliques contenant plusieurs hétérocycles, comportant des atomes d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant au moins trois hétérocycles
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
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.
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.
H10K 85/60 - Composés organiques à faible poids moléculaire
C07D 209/86 - CarbazolesCarbazoles hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du système cyclique
C07D 405/10 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 405/14 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C07D 491/048 - Systèmes condensés en ortho avec un seul atome d'oxygène comme hétéro-atome du cycle contenant de l'oxygène le cycle contenant de l'oxygène étant à cinq chaînons
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):
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.
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.
A44B 19/16 - Élément d'accrochage à section constante tout le long de la bande
B65D 33/00 - Parties constitutives ou accessoires pour sacs ou sachets
B65D 33/25 - RivetageAssemblage à queue-d'arondeVissageDispositifs de fermeture de l'extrémité ou de l'ouverture utilisant des boutons-pression ou des fermetures à glissières
B65D 75/66 - Cordons de déchirure ou éléments flexibles analogues incorporés ou ajoutés
51.
CHALCOGENIDE PEROVSKITE AND METHOD FOR PRODUCING CHALCOGENIDE PEROVSKITE BY LIQUID PHASE SYNTHESIS
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.
C07D 235/08 - Radicaux ne contenant que des atomes d'hydrogène et de carbone
C07D 401/10 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
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
C10M 115/08 - Compositions lubrifiantes caractérisées en ce que l'épaississant est un composé organique non macromoléculaire, autre qu'un acide carboxylique ou ses sels contenant de l'azote
C10N 30/06 - OnctuositéRésistance du filmAnti-usureRésistance aux pressions extrêmes
C10N 40/04 - Bains d'huileBoîtes de vitessesTransmissions automatiquesMécanismes de traction
C10N 50/10 - Forme sous laquelle est appliqué le lubrifiant au matériau à lubrifier semi-solideForme sous laquelle est appliqué le lubrifiant au matériau à lubrifier huileuse
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.
C08G 65/26 - Composés macromoléculaires obtenus par des réactions créant une liaison éther dans la chaîne principale de la macromolécule à partir d'éthers cycliques par ouverture d'un hétérocycle à partir d'éthers cycliques et d'autres composés
C09K 5/04 - Substances qui subissent un changement d'état physique lors de leur utilisation le changement d'état se faisant par passage de l'état liquide à l'état vapeur ou vice versa
C10N 20/04 - Poids moléculaireRépartition du poids moléculaire
C10N 40/30 - Lubrifiants pour machines frigorifiques
55.
ZIPPER TAPE, ZIPPER-TAPE-EQUIPPED CONTAINER, AND METHOD FOR PREVENTING FALSIFICATION
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.
B65D 33/25 - RivetageAssemblage à queue-d'arondeVissageDispositifs de fermeture de l'extrémité ou de l'ouverture utilisant des boutons-pression ou des fermetures à glissières
56.
COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
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.
C07C 211/54 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à deux ou trois cycles aromatiques à six chaînons
C07C 211/57 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons faisant partie de systèmes cycliques condensés du squelette carboné
C07C 211/61 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons faisant partie de systèmes cycliques condensés du squelette carboné avec au moins un des systèmes cycliques condensés formé par trois cycles ou plus
C07D 209/86 - CarbazolesCarbazoles hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du système cyclique
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C07D 405/12 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
C07D 405/14 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C07D 409/12 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
C07D 409/14 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
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).
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>.
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 59/32 - Dispositifs empilés comportant plusieurs couches, chacune émettant à des longueurs d'onde différentes
H10K 59/95 - Ensembles de plusieurs dispositifs comprenant au moins un élément organique émetteur de lumière dans lesquels tous les éléments émetteurs de lumière sont organiques, p. ex. ensembles d'affichages à OLED
H10K 85/60 - Composés organiques à faible poids moléculaire
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
60.
COMPOUND, ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
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.
C07D 495/22 - Composés hétérocycliques contenant dans le système condensé au moins un hétérocycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle dans lesquels le système condensé contient au moins quatre hétérocycles
C07D 209/86 - CarbazolesCarbazoles hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du système cyclique
C07D 251/24 - Composés hétérocycliques contenant des cycles triazine-1, 3, 5 non condensés avec d'autres cycles comportant trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des atomes d'hydrogène ou de carbone liés directement à au moins un atome de carbone du cycle à trois atomes de carbone du cycle
C07D 403/10 - Composés hétérocycliques contenant plusieurs hétérocycles, comportant des atomes d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 491/048 - Systèmes condensés en ortho avec un seul atome d'oxygène comme hétéro-atome du cycle contenant de l'oxygène le cycle contenant de l'oxygène étant à cinq chaînons
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 59/00 - Dispositifs intégrés, ou ensembles de plusieurs dispositifs, comprenant au moins un élément organique émetteur de lumière couvert par le groupe
H10K 85/60 - Composés organiques à faible poids moléculaire
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.
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%.
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.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
04 - Huiles et graisses industrielles; lubrifiants; combustibles
Produits et services
Coolants; dielectric fluids as a chemical preparation for cooling computer servers, except oils. Cooling lubricants; dielectric oils for cooling computer servers.
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).
C10M 171/00 - Compositions lubrifiantes caractérisées par des critères purement physiques, p. ex. contenant comme matériau de base, épaississant ou additif des ingrédients exclusivement caractérisés par des valeurs numériques particulières de leurs propriétés physiques, c.-à-d. contenant des ingrédients physiquement bien définis mais dont la nature chimique n'est pas précisée ou n'est que très vaguement indiquée
C10N 30/00 - Propriétés physiques ou chimiques particulières améliorées par l'additif caractérisant la composition lubrifiante, p. ex. additifs multifonctionnels
C07D 209/88 - CarbazolesCarbazoles hydrogénés avec des hétéro-atomes ou des atomes de carbone comportant trois liaisons à des hétéro-atomes avec au plus une liaison à un halogène, p. ex. radicaux ester ou nitrile, liés directement aux atomes de carbone du système cyclique
C07D 239/26 - Composés hétérocycliques contenant des cycles diazine-1, 3 ou diazine-1, 3 hydrogéné non condensés avec d'autres cycles comportant au moins trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du cycle
C07D 251/24 - Composés hétérocycliques contenant des cycles triazine-1, 3, 5 non condensés avec d'autres cycles comportant trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des atomes d'hydrogène ou de carbone liés directement à au moins un atome de carbone du cycle à trois atomes de carbone du cycle
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
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.
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
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.
B65D 33/25 - RivetageAssemblage à queue-d'arondeVissageDispositifs de fermeture de l'extrémité ou de l'ouverture utilisant des boutons-pression ou des fermetures à glissières
A44B 19/16 - Élément d'accrochage à section constante tout le long de la bande
B31B 70/81 - Formation ou fixation d’accessoires, p. ex. de dispositifs d’ouverture ou de fermeture, de cordons de déchirure
B31B 160/20 - Forme des réceptacles flexibles avec une configuration particulière pour tenir compte de l’épaisseur du contenu
70.
ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT DISPLAY DEVICE, AND ELECTRONIC EQUIPMENT
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
)
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).
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.
C08G 64/06 - Polycarbonates aromatiques ne contenant pas d'insaturations aliphatiques
C07C 69/757 - Esters d'acides carboxyliques dont un groupe carboxyle est lié à un atome de carbone d'un cycle autre qu'un cycle aromatique à six chaînons dont l'un des groupes OH, O-métal, —CHO, céto, éther, acyloxy, des groupes , des groupes ou des groupes se trouve dans la partie acide
C08G 64/24 - Procédés généraux de préparation utilisant des halogénures de carbonyle et des phénols
C08G 64/30 - Procédés généraux de préparation utilisant des carbonates
73.
COMPOUND, ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC 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.
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.
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).
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
C03C 10/16 - Phase cristalline contenant un halogène
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/08 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques oxydes
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.
C07C 211/61 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons faisant partie de systèmes cycliques condensés du squelette carboné avec au moins un des systèmes cycliques condensés formé par trois cycles ou plus
C07D 409/14 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
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
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
)
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.)
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
C03C 10/16 - Phase cristalline contenant un halogène
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/08 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques oxydes
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p. ex. liants, charges
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).
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).
H01L 31/05 - Moyens d’interconnexion électrique entre les cellules PV à l’intérieur du module PV, p.ex. connexion en série de cellules PV
B64G 1/44 - Aménagements ou adaptations des systèmes fournissant l'énergie utilisant des radiations, p. ex. panneaux solaires déployables
H01L 31/0392 - Dispositifs à semi-conducteurs sensibles aux rayons infrarouges, à la lumière, au rayonnement électromagnétique d'ondes plus courtes, ou au rayonnement corpusculaire, et spécialement adaptés, soit comme convertisseurs de l'énergie dudit rayonnement e; Procédés ou appareils spécialement adaptés à la fabrication ou au traitement de ces dispositifs ou de leurs parties constitutives; Leurs détails caractérisés par leurs corps semi-conducteurs caractérisés par leur structure cristalline ou par l'orientation particulière des plans cristallins comprenant des films minces déposés sur des substrats métalliques ou isolants
H01L 31/18 - Procédés ou appareils spécialement adaptés à la fabrication ou au traitement de ces dispositifs ou de leurs parties constitutives
82.
INFORMATION PROCESSING DEVICE, PROGRAM, AND INFORMATION PROCESSING METHOD
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.
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.
C07D 209/94 - Systèmes cycliques contenant au moins trois cycles condensés en [b, c] ou [b, d] contenant des carbocycles autres que des cycles à six chaînons
C07D 491/048 - Systèmes condensés en ortho avec un seul atome d'oxygène comme hétéro-atome du cycle contenant de l'oxygène le cycle contenant de l'oxygène étant à cinq chaînons
C07D 491/147 - Systèmes condensés en ortho le système condensé contenant un cycle avec l'oxygène comme hétéro-atome du cycle et deux cycles avec l'azote comme hétéro-atome du cycle
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
H10K 85/60 - Composés organiques à faible poids moléculaire
84.
COMPOUND, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 50/13 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] spécialement adaptées à l'émission de lumière multicolore, p. ex. à l'émission de lumière blanche comprenant des couches EL empilées dans une unité EL
H10K 85/60 - Composés organiques à faible poids moléculaire
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
85.
COMPOUND, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
H10K 59/00 - Dispositifs intégrés, ou ensembles de plusieurs dispositifs, comprenant au moins un élément organique émetteur de lumière couvert par le groupe
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.
H10K 85/60 - Composés organiques à faible poids moléculaire
C07C 211/54 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à deux ou trois cycles aromatiques à six chaînons
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 102/00 - Détails de structure relatifs aux dispositifs organiques couverts par la présente sous-classe
87.
MIXED POWDER FOR AN ORGANIC ELECTROLUMINESCENCE DEVICE AND METHOD FOR PRODUCING THE SAME, METHOD FOR FABRICATING ORGANIC ELECTROLUMINESCENCE DEVICE BY USING THE MIXED POWDER, METHOD FOR SELECTING COMPOUNDS IN THE MIXED POWDER, AND COMPOSITION FOR VACUUM DEPOSITION
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
)
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).
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
H10K 85/60 - Composés organiques à faible poids moléculaire
H10K 101/00 - Propriétés des matériaux organiques couverts par le groupe
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
H10K 102/00 - Détails de structure relatifs aux dispositifs organiques couverts par la présente sous-classe
89.
METHOD FOR PRODUCING AMMONIA, AND MOLYBDENUM COMPLEX USED IN PRODUCTION METHOD AND LIGAND THAT IS RAW MATERIAL FOR MOLYBDENUM COMPLEX
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.
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.
C07D 519/00 - Composés hétérocycliques contenant plusieurs systèmes de plusieurs hétérocycles déterminants condensés entre eux ou condensés avec un système carbocyclique commun non prévus dans les groupes ou
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
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.
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).
C07C 215/12 - Composés contenant des groupes amino et hydroxy liés au même squelette carboné ayant des groupes hydroxy et des groupes amino liés à des atomes de carbone acycliques du même squelette carboné le squelette carboné étant saturé et acyclique l'atome d'azote du groupe amino étant de plus lié à des groupes hydrocarbonés substitués par des groupes hydroxy
C07C 215/24 - Composés contenant des groupes amino et hydroxy liés au même squelette carboné ayant des groupes hydroxy et des groupes amino liés à des atomes de carbone acycliques du même squelette carboné le squelette carboné étant non saturé et acyclique
C10M 129/40 - Acides carboxyliquesLeurs sels comportant des groupes carboxyle liés à des atomes de carbone acycliques ou cycloaliphatiques comportant au moins 8 atomes de carbone monocarboxyliques
C10M 133/06 - Amines, p. ex. polyalkylènepolyaminesAmines quaternaires comportant des groupes amine liés à des atomes de carbone acycliques ou cycloaliphatiques
C10M 135/22 - ThiolsSulfuresPolysulfures contenant des atomes de soufre liés à des atomes de carbone acycliques ou cycloaliphatiques
C10N 30/00 - Propriétés physiques ou chimiques particulières améliorées par l'additif caractérisant la composition lubrifiante, p. ex. additifs multifonctionnels
C10N 40/04 - Bains d'huileBoîtes de vitessesTransmissions automatiquesMécanismes de traction
C10N 40/06 - Instruments ou autres appareils de précision, p. ex. fluides amortisseurs
C10N 40/08 - Fluides hydrauliques, p. ex. fluides pour freins
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.
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.
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.
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.
C08F 283/14 - Composés macromoléculaires obtenus par polymérisation de monomères sur des polymères prévus par la sous-classe sur des polymères obtenus par polymérisation avec ouverture du cycle de composés carbocycliques contenant une ou plusieurs liaisons doubles carbone-carbone dans le carbocycle, p. ex. les polyalcèneamères
C08F 8/42 - Introduction d'atomes métalliques ou de groupes contenant des atomes métalliques
C08F 277/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des polymères de monomères carbocycliques ou hétérocycliques tels que définis soit dans le groupe , soit dans le groupe
C08G 61/00 - Composés macromoléculaires obtenus par des réactions créant une liaison carbone-carbone dans la chaîne principale de la macromolécule
C08L 51/00 - Compositions contenant des polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères
C08L 65/00 - Compositions contenant des composés macromoléculaires obtenus par des réactions créant une liaison carbone-carbone dans la chaîne principaleCompositions contenant des dérivés de tels polymères
C08L 95/00 - Compositions contenant des matières bitumeuses, p. ex. asphalte, goudron ou brai
97.
ORGANIC ELECTROLUMINESCENT ELEMENT, ELECTRONIC DEVICE, AND COMPOUND
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
C07D 519/00 - Composés hétérocycliques contenant plusieurs systèmes de plusieurs hétérocycles déterminants condensés entre eux ou condensés avec un système carbocyclique commun non prévus dans les groupes ou
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
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.
H10K 85/60 - Composés organiques à faible poids moléculaire
C07C 211/54 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à deux ou trois cycles aromatiques à six chaînons
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).
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.
C07D 401/10 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07B 59/00 - Introduction d'isotopes d'éléments dans les composés organiques
C07D 401/14 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant au moins trois hétérocycles
C07D 405/14 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C07D 409/14 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
