Abstract:
An optical recording medium is disclosed, in which an optical recording layer (2) and a reflective layer (3) are formed on a transparent substrate. The recording layer (2) contains a first compound having absorption or a recording laser light having a predetermined wavelength, and a second compound having substantially no absorption for a laser light having the predetermined wavelength and decomposable upon heat generation by the laser light in the optical recording layer.
Abstract:
An optical recording medium is disclosed, in which an optical recording layer (2) and a reflective layer (3) are formed on a transparent substrate. The recording layer (2) contains a first compound having absorption or a recording laser light having a predetermined wavelength, and a second compound having substantially no absorption for a laser light having the predetermined wavelength and decomposable upon heat generation by the laser light in the optical recording layer.
Abstract:
PROBLEM TO BE SOLVED: To provide an organic electroluminescent device which has a high fluorescence yield, and excellent red color purity, high brightness and stable red luminescence using a compound excellent also in heat stability. SOLUTION: In the organic electroluminescent device, on a glass substrate 1, an ITO transparent electrode 2, a hole transport layer 6, an electron transport layer 7, and a metal electrode 3 are laminated in this order, the hole transport layer 6 and/or the electron transport layer 7 consist of an aminostyryl compound expressed with general formula [I], and a hole blocking layer 30 is provided between the hole transport layer 6 and the electron transport layer 7. In the general formula [I] where X 1 is aryl group, such as phenyl group with substituent, such as nitro group, and Y 1 and Y 2 are groups having aminophenyl group, etc. in their skeletons. COPYRIGHT: (C)2010,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a bis(aminostyryl)benzene compound developing intense luminescence and applicable as an yellow to red luminous material. SOLUTION: A bis(aminostyryl)benzene compound represented by general formula [XIX] is provided (wherein R 90 , R 91 , R 92 and R 93 are the same or different group each other, at least one of which is a specific (substituted) aryl group, the others are an unsubstituted aryl group, and the substituent of the central benzene ring is a fluorine atom). COPYRIGHT: (C)2009,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To obtain an anthracene derivative that is preferably useful as a blue luminescent material for an organic electroluminescent element and provides an organic electroluminescent element having high luminous efficiency and excellent life properties. SOLUTION: The anthracene derivative is represented by general formula (1) (X is an arylene group or a bifunctional heterocyclic group; A and B are each an alkyl group, an aryl group or a heterocyclic group and A and B may be mutually bonded to form a ring; Y 1 and Y 2 are each a hydrogen atom, an alkyl group or an alkoxy group; C is an aryl group, a heterocyclic group, a hydrogen atom, an alkyl group or an alkoxy group). COPYRIGHT: (C)2006,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide an organic material which has high luminous efficiency and excellent luminous life, to provide an organic electroluminescent element using the organic material, and to provide a display device using the organic electroluminescent element. SOLUTION: The organic material used for organic electroluminescent elements is a chrysene represented by the general formula (1). COPYRIGHT: (C)2006,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide an organic material which has high luminous efficiency and excellent luminous life, to provide an organic electroluminescent element using the organic material, and to provide a display device using the organic electroluminescent element. SOLUTION: The organic material used for organic electroluminescent elements and represented by the general formula (1) (A 1 to A 24 are each independently H, a halogen, OH, a ≤20C substituted or non-substituted carbonyl, a ≤20C substituted or non-substituted carbonyl ester, a ≤20C substituted or non-substituted alkyl, a ≤20C substituted or non-substituted alkenyl, a ≤20C substituted or non-substituted alkoxyl, a ≤30C substituted or non-substituted aryl, a ≤30C substituted or non-substituted heterocyclic group, cyano, nitro, or a ≤20C substituted or non-substituted silyl). COPYRIGHT: (C)2006,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide an organic material capable of being prevented from deteriorating and capable of being improved in driving efficiency, and to provide an organic element by using the organic material. SOLUTION: The organic material is used for the organic element, wherein a concentration of palladium contained in the organic material is not more than 1000 ppm. The organic material is used for a positive hole injection layer 14a, a positive hole transport layer 14b, and a light-emitting layer 14c in the organic EL element 11. COPYRIGHT: (C)2005,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide a preserving method of an organic material for an organic electroluminescent element which enables to suppress the deterioration of the organic material for the organic electroluminescent element in a preserved state. SOLUTION: On the preserving method of the organic material for an organic EL element, the organic material used for a positive hole transporting layer 13, a light emitting layer 14, and an electron transporting layer 15 of the organic EL element 10 is preserved under an atmosphere in which oxygen gas concentration is made lower than that of air, further, the organic material is housed in a packing body having inert gas atmosphere at its inside. COPYRIGHT: (C)2005,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide an organic EL light emitting element provided with a light emitting region layer having a newly developed oligonaphthalene compound and a stable blue color light emitting function. SOLUTION: This organic EL light emitting element is provided with the light emitting region layer containing the oligonaphthalene compound expressed by the figure (2). COPYRIGHT: (C)2005,JPO&NCIPI