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JP4782130B2 |
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JP4772280B2 |
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JP4743673B2 |
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JP2011521894A |
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JP4733334B2 |
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JP2011518133A |
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JP4699756B2 |
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JP2011105645A |
To provide a photoacid generator having high developability, a cationic polymerization initiator having high curability, a resist composition and a cationically polymerizable composition using them.An aromatic sulfonium salt compound rep...
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JP4683675B2 |
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JP4686126B2 |
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JP2011084586A |
To develop novel polyamine analogues for various applications.The present invention provides novel polyamine analogues, compositions comprising these polyamine analogues, and methods of using the analogues and the compositions. In one em...
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JP4672144B2 |
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JP2011075785A |
To provide an electrophotographic photoreceptor with excellent photo sensitivity and filming resistance.The electrophotographic photoreceptor including a photosensitive layer on a conductive substrate contains an acridone derivative repr...
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JP2011509994A |
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JP4652054B2 |
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JP4653216B2 |
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JP4646494B2 |
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JP2011026376A |
To provide a dye-sensitized type battery having high conversion efficiency by using an inexpensive organic dye.The dye has a structure expressed by general formula (1). In the formula, X represents an oxygen atom, a sulfur atom or CR2(R3...
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JP4630405B2 |
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JP2011503235A |
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JP2011006559A |
To provide an inexpensive pigment compound capable of achieving a high photoelectric conversion ratio, accessible without remarkable restriction, a photoelectric conversion element and a solar battery using the same.The pigment compound ...
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JP4601234B2 |
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JP4601293B2 |
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JP2010280512A |
To provide an inorganic-organic composite material capable of attaining a charge-separated state enhanced in life and stability as compared with that of conventional inorganic-organic composite materials.The inorganic-organic composite m...
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JP4585750B2 |
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JP4583027B2 |
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JP4573533B2 |
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JP4570364B2 |
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JP2010533182A |
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JP2010237226A |
To provide a method for the measurement of hydride using a chemiluminescent compound, such as an acridinium compound. The source of hydride may be of chemical or biochemical origin, or the result of enzymatic catalysis. The chemical sour...
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JP2010215633A |
To identify two sets of necessary and sufficient criteria for observing long-wavelength emission from an acridinium compound.The two sets, i.e. set (A) and set (B), of necessary and sufficient criteria for observing long-wavelength emiss...
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JP4551502B2 |
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JP4542838B2 |
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JP4546090B2 |
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JP4536714B2 |
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JP4531149B2 |
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JP2010180204A |
To provide a charge transport material having high chemical stability and large T1 (lowest excited triplet energy level), and to provide a highly efficient organic electroluminescent (EL) device having a low driving voltage, and even hig...
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JP4524186B2 |
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JP2010523601A |
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JP4503833B2 |
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JP2010150518A |
To provide a polymeric compound useful for producing a light-emitting element excellent in the external quantum yield in the luminance of 1,000 cd/m2. There is disclosed a polymeric compound having a constituent unit represented by formu...
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JP2010520884A |
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JP2010132638A |
To provide a new organic electroluminescent compound and an organic electroluminescent element by using the same. This organic electroluminescent compound is expressed by chemical formula 1 [wherein, among Ar1, Ar2, R6, R7, R8, R9, R10, ...
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JP2010100647A |
To provide ionic compounds, derivatives of malononitrile, in which the anionic charge has been displaced.The ionic compound includes an anionic portion combined with at least one cationic portion M+m in numbers enough to ensure overall e...
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JP2010100622A |
To provide a compound that upregulates manifestation of endothelial NO-synthase.There are provided acylated indanyl amines represented by general formula (I) [wherein R1 to R4 are each independently selected from the group consisting of ...
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JP2010095527A |
To provide compounds for inactivating pathogens in materials.Compounds and methods for inactivating pathogens in materials are described, including compositions and methods for inactivating pathogens in red blood cell preparations and bi...
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JP2010065033A |
To provide a new organic electroluminescent compound.The new organic electroluminescent compound is represented by chemical formula (1) (wherein, Ar is 6-60C arylene, 3-60C heteroarylene containing one or more heteroatoms selected from N...
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JP4439265B2 |
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JP2010059144A |
To provide a new organic electroluminescent compound and an organic electroluminescent device using it as an electroluminescent material.The compound is represented by chemical formula 1, (wherein, ring A and ring B indicate each indepen...
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JP2010059158A |
To provide a new organic electroluminescent compound and an organic electroluminescent device, etc., containing the compound.The electroluminescent compound is expressed by chemical formula 1 (wherein R1 to R10 are each H or a substituen...
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