Abstract: Any of the oligoaniline compounds with a triphenylamine structure represented by the formula (1) exhibits satisfactory light emitting efficiency and brightness performance when used in either an OLED device or a PLED device and is further satisfactory in the solubility in organic solvents so as to be applicable to various coating methods. (each of R1 and R2 independently is a hydrogen atom, an optionally substituted monovalent hydrocarbon group, t-butoxycarbonyl, etc.; each of R3 to R34 independently is a hydrogen atom, hydroxyl, silanol, thiol, carboxyl, a phosphoric group, a phosphoric ester group, ester, thioester, amido, nitro, an optionally substituted monovalent hydrocarbon group, etc.; and each of m and n is an integer of 1 or greater provided that they satisfy the relationship m+n?20).

Abstract: Improved methods for making hole transport molecules (HTMs) that are incorporated into imaging members, such as layered photoreceptor devices, to increase the photoreceptor's “hole mobility,” or its ability to move charge, across its charge transport layer (CTL). Embodiments pertain to a continuous process for making N,N-diphenyl-4-biphenylamine and a system for performing the same.

Abstract: The present invention relates to a new diamine derivative, and an organic electronic device using the same. The diamine derivative according to the present invention can serve as a hole injecting, hole transporting, electron injecting, electron transporting, or light emitting material in an organic electronic device including an organic light emitting device. Particularly, it can serve as a light emitting dopant as used alone, in particular, a blue light emitting dopant. The organic electronic device according to the present invention exhibits excellent characteristics in terms of efficiency, drive voltage, life time, and stability.

Abstract: Provided are arylamine compounds having Formula I, II, III, or IV: wherein Ar is the same or different at each occurrence and is aryl having from 6 to 30 carbon atoms or heteroaryl having from 2 to 30 carbon atoms. Also provided are compositions comprising arylamine compounds. The invention also relates to use of such compounds in electronic devices, for example, organic electronic devices.

Abstract: Disclosed herein are novel compounds and pharmaceutical compositions comprising these compounds. In some embodiments, the compounds are inhibitors of the tryptase enzyme and are useful for treating allergic rhinitis, asthma, vascular injury (e.g., restenosis and atherosclerosis), inflammatory bowel disease, arthritis, psoriasis, anaphylaxis, wounds, infections, and other allergy and inflammatory related diseases.

Abstract: Novel monoaminofluorene compounds are provided, and organic light-emitting devices which exhibit good luminescence hue of extremely high purity and have optical output with high luminescence efficiency, high luminance and longer operating life are provided using the compounds.

Abstract: By using an amine hydrochloride represented by the formula (1) as a catalyst, a polythiourethane resin which is suitably used for a transparent resin for optical use, can be obtained without using an organotin compound which has been conventionally used as a catalyst for polythiourethane resins and without being affected by the acidity of an additive: wherein R1, R2 and R3 independently represent a monovalent or higher valent linear aliphatic, branched aliphatic, cyclic aliphatic or aromatic organic residue which may have a hydroxyl group or an amino group; and R1, R2 and R3 may be arbitrarily bonded to each other to form a ring.

Abstract: The present invention provides an organic electroluminescent device exhibiting a long life, a high luminance, and a high efficiency. An organic electroluminescent device comprising on a substrate an anode, a hole transport layer, an organic light-emitting layer, and a cathode, wherein the organic light-emitting layer contains an organic compound having a pyridine ring, a pyrazine ring, or a triazine ring as a partial structure and the hole transport layer contains a monoamine compound represented by the following formula (I): wherein R1 to R9 represent a hydrogen atom, an aryl group, or an alkyl group; R1 to R9 may be the same or different from each other; and R1 to R9 may further have an aryl group or an alkyl group as a substituent in the case where R1 to R9 are an aryl group or an alkyl group.

Abstract: A crosslinking monomer for making a crosslinked polymer, said monomer comprising reactive leaving groups Y and Y1 located on the same or different aryl or heteroaryl groups of the monomer and a structural unit of general formula I: where Ar represents an aryl or heteroaryl group; Ar1 and Ar2 each independently represents a substituted or unsubstituted aryl or heteroaryl group and where any two of Ar, Ar1 and Ar2 may optionally be linked; Sp represents an optional spacer group; and X represents a crosslinkable group.

Abstract: The invention comprises lubricating compositions and hydraulic fluids containing N,N?-diaryl-p-phenylene diamine compounds that impart good levels of oxidation inhibition in the lubricants and hydraulic fluids.

Abstract: A pulsed driven display comprising an organic light-emitting device, said device comprising an organic layer comprising a semiconductive polymer, said polymer comprising a fluorene or triarylamine repeat unit, the fluorene or triarylamine repeat unit having a group R pendent from the polymer backbone, wherein R has general formula I: where Ar1 represents phenyl or a group comprising napthyl; Ar2 represents phenyl or a group comprising napthyl; R? represents a substituent group; R??H or a substituent; n=0, 1, 2 or 3; m=0 or 1; and n?=1 or 2, with the proviso that m=0 if n=0.

Abstract: Disclosed herein is a method for reducing the oxidative and biological degradation of a metalworking fluid comprising adding thereto at least one antioxidant and at least one biocide.

Abstract: An amine compound represented by the general formula (1), which is incorporated as a charge-transporting substance to a charge-transporting layer of an electrophotographic photoreceptor: (in which Ar1, Ar2 and Ar3 each represents an optionally-substituted aryl group, or an optionally-substituted monovalent heterocyclic ring residue. Ar4 represents an optionally-substituted arylene group, or an optionally-substituted bivalent heterocyclic ring residue. R1 represents an optionally-substituted alkyl group, an optionally-substituted aryl group, an optionally-substituted monovalent heterocyclic ring residue, or an optionally-substituted aralkyl group. R2 and R3 each represents a hydrogen atom, an optionally-substituted alkyl group, an optionally-substituted aryl group, an optionally-substituted monovalent heterocyclic ring residue, or an optionally-substituted aralkyl group. n represents an integer of 1 or 2.

Abstract: The object is to provide a light-emitting transistor material which is high in both luminescent property and mobility when used as a light-emitting transistor device. A light-emitting transistor device is provided in which light emission of a specific pyrene-based organic compound is used for a light-emitting layer of a transistor device.

Abstract: An organic electroluminescent device comprises a cathode, an anode, and has therebetween a light-emitting layer comprising an emissive component represented by formula (I): wherein: Ar1, each Ar2, and Ar3 through Ar7 are independently selected aryl or heteroaryl groups, which may contain additional fused rings and provided that two aryl or heteroaryl rings may be joined; n is 1, 2 or 3. The device exhibits good luminous yield with desirable color coordinates, particularly in the blue or blue-green region.

Abstract: It is an object of the present invention to provide a luminescent material that has resistance to repeated oxidation reactions. Further, it is an object of the present invention to provide a light-emitting element that is high in luminous efficiency. Further, it is an object of the present invention to provide a light-emitting element that has a long life. An aspect of the present invention is an anthracene derivative represented by a general formula (1). In the general formula (1), R2 to R4 and R7 to R9 are individually any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, and a group represented by the following structure formula (2), and R1, R5, R6, and R10 are individually any one of hydrogen and an alkyl group having 1 to 4 carbon atoms.

Abstract: This invention relates to novel substituted phenylamino-benzene compounds, pharmaceutical compositions containing such compounds and the use of those compounds or compositions for treating hyper-proliferative and/or angiogenesis disorders, as a sole agent or in combination with other active ingredients.

Abstract: The invention is directed to a method of producing one or more 4-aminodiphenylamine intermediates comprising the steps: a. bringing an aniline or aniline derivative and nitrobenzene into reactive contact; and b. reacting the aniline and nitrobenzene in a confined zone at a suitable time and temperature, in the presence of a mixture comprising a strong organic base, or equivalent thereof, and an oxidant comprising hydrogen peroxide in an amount of from about 0.01 to about 0.60 moles of hydrogen peroxide to moles of nitrobenzene.

Abstract: A semiconductive polymer comprising a first repeat unit in the polymer backbone comprising general formula 1: where a=1 or 2; b=0 or 1; and c=0, 1 or 2, provided that when c=0 then b=0; Ar1, Ar2, Ar3, Ar4, Ar5, and Ar6 each independently represent an aryl or heteroaryl ring or a fused derivative thereof; characterised in that at least one of Ar1, Ar2, Ar4, and Ar5 is non-conjugating; and provided that (a) when a=1, Ar1 is not linked to Ar2 by a direct bond, (b) when b=1 and c=1, Ar4 is not linked to Ar5 by a direct bond, (c) when b=0 and c=1, Ar2 is not linked to Ar5 by a direct bond, (d) when a=2, the Ar1 groups are not linked by a single bond, and (e) when c=2, the Ar5 groups are not linked by a single bond.

Abstract: The present invention relates to the improvement of blue-emitting organic electroluminescent devices comprising stilbenamines, and to materials for the production of these electroluminescent devices.

Abstract: The invention comprises lubricating compositions and hydraulic fluids containing N,N?-diaryl-p-phenylene diamine compounds that impart good levels of oxidation inhibition in the lubricants and hydraulic fluids.

Abstract: Antioxidants for industrial, automotive, and aviation lubricants and methods of making the same are provided. A process using alkylated diphenylamines; alkylated phenyl-?-naphthyl amines; and a metal catalyst to form oxidates is provided. The metal catalyst is a combination of a cation and an organic anion, for example, a metal acetylacetone. The reaction takes place in the presence of oxygen to form an antioxidant comprising oligomers of the alkylated diphenylamine and the alkylated phenyl-?-naphthyl amine, and a metal component of the catalyst.

Abstract: A process for forming a tetra(aryl)-biphenyldiamine compound, including reacting a dibromobiphenyl compound and a diarylamine compound in the presence of a palladium ligated catalyst and a base.

Abstract: An organic electroluminescent device includes an anode, a cathode, and an organic layer having a light-emitting area and arranged between the anode and the cathode. The organic layer contains in at least a part thereof at least one aminostyrylnaphthalene compound represented by the following formula [I], [II] or [III]: wherein R1, R2, R11, R12, R23 and R24 are each a phenyl or naphthyl group, R3, R4, R13, R14, R25 and R26 are each an electron attracting group such as a cyano group, and R5, R15 and R27 are each a substituent group such as an alkyl group.

Abstract: A process including reacting a substituted or unsubstituted arylamine or a mixture thereof with a Vilsmeier reagent in the presence of a weakly polar liquid.

Abstract: A process for alkylation of a N?-phenyl-N-alkyl-p-phenylenediamine of specified formula in an ionic liquid unexpectedly produces a N?-phenyl-N-alkyl(alkylphenylene)diamine of a second specified formula. The use of an inorganic liquid permits convenient separation of the alkylated reaction product from the reaction mixture.

Abstract: The present invention provides analogs of a Lysofylline (LSF), and synthetic methods for the preparation of such analogs. The have the active side chain moiety (5-R-hydroxyhexyl) of LSF and can have greater potency and oral bioavailability than LSF.

Abstract: A hole transporting or hole conducting material for use in electroluminescent devices is a diamino dianthracene.

Abstract: It is an object of the present invention to provide a light-emitting substance which is resistant to repetition of an oxidation reaction. It is another object of the invention to provide a light-emitting element which is resistant to repetition of a reduction reaction. An aspect of the present invention is an anthracene derivative represented by a general formula (1). In the general formula (1), R1 represents hydrogen or an alkyl group having 1 to 4 carbon atoms; R2 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, and an aryl group having 6 to 12 carbon atoms, which may have a substituent or no substituent; Ph1 represents a phenyl group, which may have a substituent or no substituent; and X1 represents an arylene group having 6 to 15 carbon atoms.

Abstract: Provided are a compound represented by Formula 1 below and an organic light-emitting device including the same: wherein X is a C, Si, or Ge atom disubstituted with H or C1-60 organic groups, Ra-Rj are C1-60 organic groups, CY1 is a substituted or unsubstituted C5-C60 aromatic ring or a substituted or unsubstituted C2-C60 heteroaromatic ring, and n is 0 or 1. The use of the compound provides an organic light-emitting device having a low operating voltage and good efficiency and brightness.

Abstract: A process including reacting a substituted or unsubstituted arylamine or a mixture thereof with a Vilsmeier reagent in the presence of a weakly polar liquid.

Abstract: A process comprising for example reacting a substituted or unsubstituted arylamine or a mixture thereof with a Vilsmeier reagent in a solvent system comprising acetonitrile as a sole solvent or a solvent system comprising acetonitrile and one or more solvents selected from toluene, xylene, chlorobenzene, dichlorobenzene, dichloromethane, 1,2-dichloroethane, or a combination thereof.

Abstract: An anthracene compound for an organic electroluminescent device, having formula (I) or (II) wherein R1, R2, R3, R4, R5, and R6 are each individually an unsubstituted or substituted aryl group having 6 to 20 carbon atoms, an unsubstituted or substituted heteroaryl group having 6 to 20 carbon atoms, or an unsubstituted or substituted alkyl group having 1 to 12 carbon atoms, wherein the substituent is C1-10 alkyl, C1-10 alkoxy, or halogen.

Abstract: The present invention relates to a process for preparing aryl-aryl-coupled compounds and materials. These materials play an important role in industry, for instance as liquid crystals, pharmaceuticals, agrochemicals and as organic semiconductors. The aryl-aryl couplings hitherto carried out by means of Yamamoto coupling require specific additives in order to give a product suitable for the subsequent use. Particularly in the electronics industry, the Yamamoto coupling needs to meet particular requirements.

Abstract: Elastomers which have excellent stability to prevent oxidative, thermal, dynamic, light-induced and/or ozone-induced degradation comprise, as stabilizers, at least one compound of the formula I [R—S(?O)m—CH2—CH(OH)—CH2]n—N(R1)2-n—R2, ??(I) in which R is C4–C20alkyl, hydroxyl-substituted C4–C20alkyl; phenyl, benzyl, ?-methylbenzyl, ?,?-dimethylbenzyl, cyclohexyl or —(CH2)qCOOR3, and, if m is 0, R may additionally be and, if n is 1 and R4 is hydrogen, R may additionally be R2—R1N—CH2—CH(OH)—CH2—S(?O)m—(CH2)x— or R2—R1N—CH2—CH(OH)—CH2—S(?O)m—CH2—CH2—(O—CH2—CH2)y—, R1 is hydrogen, cyclohexyl or C3–C12alkyl, R2 is R3 is C1-C18alkyl, R4 is hydrogen or —CH2—CH(OH)—CH2—S(?O)m—R, X is C1–C8alkyl, Y is C1–C8alkyl, m is 0 or 1, n is 1 or 2, q is 1 or 2, x is from 2 to 6, and y is 1 or 2. The compounds of the formula I are also suitable as stabilizers for elastomers to prevent contact discoloration of substrates coming into contact with elastomers.

Abstract: The invention is directed to a method of producing one or more 4-aminodiphenylamine intermediates comprising the steps: a. bringing an aniline or aniline derivative and nitrobenzene into reactive contact; and b. reacting the aniline and nitrobenzene in a confined zone at a suitable time and temperature, in the presence of a mixture comprising a strong organic base, or equivalent thereof, and an oxidant comprising hydrogen peroxide in an amount of from about 0.01 to about 0.60 moles of hydrogen peroxide to moles of nitrobenzene.

Abstract: Novel styryl compounds represented by the following general formulae (1) and (2): wherein R1 to R10 each independently represent hydrogen atom, an alkyl group, an alkoxyl group, an aryl group, an aryloxyl group, a condensed polycyclic group, a heterocyclic group, amino group, an alkylamino group, an arylamino group, cyano group, nitro group, hydroxyl group or a halogen atom, adjacent groups among groups represented by R1 to R10 may be bonded to each other and form a saturated or unsaturated carbon ring, and A, B, C, D, A?, B?, C? and D? each independently represent a substituted or unsubstituted alkyl group or aryl group having a specific structure; and an organic electroluminescence device comprising a film of organic compounds comprising at least a light emitting layer, wherein at least one of the layers of the film of organic compounds comprises the novel styryl compound.

Abstract: Image formation via photoinduced fluorescence changes in a polymeric medium with two-photon fluorescence readout of a multi-layer structure. Fluorophore-containing polymers, possessing one or more basic functional groups, underwent protonation in the presence of a photoinduced acid generator upon exposure to a broad-band UV light source or fast-pulsed red to near-IR laser irradiation. Solution studies demonstrated formation of monoprotonated and diprotonated species upon irradiation, each resulting in distinctly different absorption and fluorescence properties. The fluorescence of the original, neutral, fluorophore was reduced upon monoprotonation, leading to a concomitant increase in fluorescence at longer wavelengths due to the monoprotonated form, the basis for multichannel data readout.

Abstract: A biphenyl derivative having an amino group with or without alkoxy substituent in the biphenyl backbone, and an organic electroluminescent device using the same.

Abstract: (?)-3-[3-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-yloxy]-4-methoxyanilino]-2-methyl-2-cyclopenten-1-one, or its hydrate or solvate, or a pharmaceutical composition containing the same.

Abstract: An electroluminescent element in which at least one layer containing at least one of novel hydrocarbon compounds with an anthracene ring and a fluorene ring directly bound is held between a pair of electrodes. The compounds can advantageously be used in a luminescent element and provide an organic electroluminescent element having an excellent luminescent efficiency and a long luminescent life.

Abstract: A bis(aminostyryl)naphthalene compound represented by the general formula [I] or the like below. (where R2 and R3 each denotes an unsubstituted aryl group; R1 and R4 each denotes an aryl group having a specific substituent such as methoxy group; and R5 and R6 each denotes a cyano group or the like.) A process for producing a bis(aminostyryl)naphthalene compound represented by the general formula [I] by condensation of, for example, 4-(N,N-diarylamino)benzaldehyde with diphosphonic ester or diphosphonium. The bis(aminostyryl)naphthalene compound emits intense yellow or red light. The process permits efficient production of the bis(aminostyryl)naphthalene compound.

Abstract: An organic electroluminescent device includes an anode, a cathode, and an organic layer having a light-emitting area and arranged between the anode and the cathode.

Abstract: The invention provides organic compounds of the general structures (1A), (1B) and (1C) 1

Abstract: An organic material capable of generating luminescence by charge of an electric current includes a compound having a general formula (1): wherein Ar1, Ar2 and Ar3 may be the same or different and, respectively, represent a substituted or unsubstituted aryl group or heterocyclic aryl group and wherein R1, R2, R3, and R4 may be the same or different and, respectively, represent a alkyl group, cycloalkyl group, a substituted or unsubstituted aryl group or heterocyclic aryl group.

Abstract: The present invention relates to processes for the facile synthesis of diaryl amines and analogues thereof. The processes of the present invention produce diaryl amines in high yield and purity. The present invention also relates to intermediates useful in the process of the present invention.

Abstract: A biphenyl derivative having an amino group with or without alkoxy substituent in the biphenyl backbone, and an organic electroluminescent device using the same.

Abstract: Disclosed herein is a process for the preparation of alkylated diarylamines comprising adding to said diarylamine an olefin mixture containing highly reactive fractions, as well as fractions exhibiting a relatively lower chemical reactivity, in the presence of an acidic clay catalyst at a temperature low enough to prevent substantial deactivation of the catalyst until the addition is complete and then increasing the temperature to increase the alkylation rate of the less reactive fractions.

Abstract: The invention is directed to a method of producing one or more 4-aminodiphenylamine intermediates comprising the steps:

Abstract: Compounds of formula I and pharmaceutically-acceptable and -cleavable esters thereof and acid addition salts thereof wherein the symbols are as defined are MAP kinase inhibitors, useful pharmaceutically for treating TNF&agr; and IL-1 mediated diseases such as rheumatoid arthritis and diseases of bone metabolism, e.g. osteoporosis.