子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 221 | Photogenerating azo pigment | JP8473393 | 1993-04-12 | JPH0641451A | 1994-02-15 | KOTSUKU II ROU; IHOO DABURIYUU TAANAUSUKII |
| PURPOSE: To prepare a non-toxic photogenerating azo pigment producing a picture-forming material having a high cycle stability, a high sensitivity, a low dark-attenuation and an excellent all-colority in an economic process by coupling an aromatic amine with a specified methoxy coupler. CONSTITUTION: A photogenerating azo pigment of formula II (wherein A is a residue structure of an aromatic amine; (p) is a positive integer, and (m) is an integer of from about 0 to 4; (x) is an organic or inorganic substituent) is prepared by coupling an aromatic amine with a methoxy coupler of formula I wherein X is F, Cl, Br, NO 2, CN, OH, NH 2, OCH 3, OCH 2CH 3, CF 3 an alkyl or an aromatic group; (m) is 0, 1, 2, 3 or 4; the methoxy group is located at fifth, sixth, seventh or eighth carbon atom of the second ring of naphthanilido. COPYRIGHT: (C)1994,JPO | ||||||
| 222 | JPH0549983B2 - | JP26843990 | 1990-10-08 | JPH0549983B2 | 1993-07-27 | AKAO AKIO; KUWAKUBO SEIJI; KADOI TAKEO |
| 223 | Bisazo derivative and its intermediate | JP23839091 | 1991-09-18 | JPH0578363A | 1993-03-30 | MIZUTA YASUSHI |
| PURPOSE:To provide a new compound useful as an electric charge-generating material excellent in electric charge-generating efficiency. CONSTITUTION:The objective compound of formula I (R<1> and R<2> are each H or lower alkyl; Cp<1> and Cp<2> are each coupler residue). This compound can be obtained by reaction of a diazo compound of formula II (R<3> and R<4> are each halogen or BF4) with a coupler in a solvent (e.g. dimethylformamide) in the presence of a base (e.g. sodium acetate) at ca.20 deg.C for 3-10hr. The compound, when used as an electric charge-generating material, is highly sensitive in the visible ray region, thus providing high-performance electronic devices; furthermore, because of being easy to handle in terms of synthesis and high in the solubility to solvents, the compound can be used easily, being also usable for coloring pigments, organic photosensitizers, solar cells, or electronic devices such as photoelectric transfer elements and optical information memorizing elements. | ||||||
| 224 | Bisazo derivative and its intermediate | JP23839491 | 1991-09-18 | JPH0578361A | 1993-03-30 | MIZUTA YASUSHI; MIYAMOTO EIICHI |
| PURPOSE:To provide a novel compound useful 0as an electric charge-generating material excellent in electric charge-generating efficiency. CONSTITUTION:The objective compound of formula I (R<1> and R<2> are each 0 or S; R<3> and R<4> are each H, alkyl or aryl; (m) and (n) are each 0-2; Cp<1> and Cp<2> are each coupler residue). The present compound can be obtained by reaction of a diazo compound of formula II (R<5> and R<6> are each halogen or BF4) with a coupler in a solvent (e.g. dimethylformamide) in the presence of a base (e.g. sodium hydroxide) at ca.20 deg.C for 3-5hr. The present compound, when used as an electric charge-generating material, is highly sensitive in the visible ray region, thus providing high-performance devices; and being also usable for coloring pigments, organic photosensitizers, solar cells, photoelectric transfer elements, optical information memorizing elements, etc. | ||||||
| 225 | JPH0515263B2 - | JP13817386 | 1986-06-16 | JPH0515263B2 | 1993-03-01 | AKASAKI YUTAKA; TOKIDA AKIHIKO; TORIGOE KAORU; IMAI AKIRA; ISHII TOORU |
| 226 | Triphendioxazine dyestuff | JP13175291 | 1991-04-18 | JPH04227662A | 1992-08-17 | HORUSUTO IEEGAA |
| PURPOSE: To obtain a novel triphendioxazine dyestuff useful for dyeing and printing a cellulose-containing and amide-containing substances by selecting a specific triphendioxazine dyestuff. CONSTITUTION: The dyestuffs represented by formula I [wherein R is H or (substd.) 1-6C alkyl, R 1 is H or a substituent, T 1 and T 2 are H, Cl, Br, (substd.) 1-4C alkyl, (substd.) 1-4C alkoxy, (substd.) phenyl or (substd.) phenoxy, Y is (substd.) amino, (thio) ether, H, (substd.) lower alkyl or (substd.) phenyl, n is 0-1 and a sulfo group wherein n is 1 is present at an ortho position with respect to groups represented by formulae II-III] are selected. These dyestuffs are pref. obtained by reacting a compd. represented by formula V (Hal is F, Cl or Br) and a compd. represented by formula H-X [X 1 is (substd.) amino or (thio) ether] with a compd. represented by formula IV. COPYRIGHT: (C)1992,JPO | ||||||
| 227 | JPH0326383B2 - | JP4302582 | 1982-03-19 | JPH0326383B2 | 1991-04-10 | FURITSUTSU GURAASAA; GEERUHARUTO HOFUMAN; RAINHORUTO IYOTSUTO REIRAA; PEETAA NOIMAN; MANFUREETO PACHI |
| 228 | Preparation of 4-chlorothiazolyl-containing azo disperse dye | JP23589689 | 1989-09-13 | JPH02242859A | 1990-09-27 | ROBERUTO EGURI |
| PURPOSE: To obtain a 4-chlorothiazolyl-containing azo disperse dye useful in dyeing polyester fibers and wool by diazotizing a specified amine and coupling the product with a specified compound. CONSTITUTION: An amine represented by formula I {wherein R is -CHO, -CH= C(CN)-R 1, [wherein R 1 is a (substituted) 1-10C alkoxycarbonyl or the like], -CN, -CH=CH-R 2 [wherein R 2 is a (substituted) phenyl or benzoyl], -CH=NOH, -CH=C(R 3)NO 2 (wherein R 3 is H, methyl or ethyl); and m is 0 or 1} is diazotized, and the product is coupled with a compound represented by the formula: H-K (wherein K is a group of a coupling component in the series of aniline, α-naphthylamine, pyrazole, aminopyrazole, indole, tetrahydroquinoline, thiazole, phenol, naphthol, pyridine and pyridone) to obtain the purpose compound represented by formula II. COPYRIGHT: (C)1990,JPO | ||||||
| 229 | Electrophotographic sensitive body | JP3112789 | 1989-02-13 | JPH02211454A | 1990-08-22 | KAWAHARA TATSURO |
| PURPOSE: To improve the sensitivity and durability of the photosensitive body by using a specific compd. as a photoconductive material. CONSTITUTION: The dis-azo compd. expressed by formula I is used as the photoconductive material of this photosensitive body. In the formula, Cp denotes a residual coupler group and the groups expressed by formulas II, III, etc., are preferably used for Cp. In the formula, X denotes a (substd.) hydrocarbon ring, heterocycle; Y denotes H, -CON(-R 1)-R 2, etc.; R 1 to R 3 denote H, (substd.) hydrocarbon group, etc. The photosensitive body is formed by applying a dispersion contg. the compd. expressed by the formula and a phenoxy resin on a conductive substrate to form a charge generating layer and applying a soln. contg. a charge transfer material and polycarbonate thereon to form a charge transfer layer. COPYRIGHT: (C)1990,JPO&Japio | ||||||
| 230 | Electrophotographic sensitive body | JP3112689 | 1989-02-13 | JPH02211453A | 1990-08-22 | KAWAHARA TATSURO |
| PURPOSE: To improve the sensitivity and durability of the photosensitive body by incorporating a specific dis-azo compd. into a photosensitive layer. CONSTITUTION: The dis-azo compd. expressed by formula I is incorporated as a photoconductive material into this photosensitive body. In the formula, Cp denotes a residual coupler group and the groups expressed by formulas II, III, etc., are preferably used for Cp. In the formula, X denotes a (substd.) hydrocarbon ring, heterocycle; Y denotes H, -CON(-R 1)-R 2, etc.; R 1 to R 3 denote H, (substd.) hydrocarbon group, etc. The photosensitive body is formed by applying a dispersion contg. the compd. expressed by the formula and a polyester resin on, for example, a polyester film deposited by evaporation with aluminum. COPYRIGHT: (C)1990,JPO&Japio | ||||||
| 231 | Electrophotographic sensitive body | JP2993089 | 1989-02-10 | JPH02210454A | 1990-08-21 | KAWAHARA TATSURO |
| PURPOSE: To obtain such high sensitivity and durability as to make a sensitive body withstand practical use by incorporating a specified compd. CONSTITUTION: A compd. represented by formula I (where Cp is a residue of a coupler) is incorporated. For example, a photosensitive layer 2a contg. the disazo compd. 3 dispersed in a binder 4 is formed on an electrically conductive support 1 or a photosensitive layer 2b contg. the disazo compd. 3 dispersed in an electric charge transferring medium consisting of an electric charge transferring material 5 and a binder is formed on the support 1. The durability of the resulting sensitive body is improved and high sensitivity can be obtd. COPYRIGHT: (C)1990,JPO&Japio | ||||||
| 232 | Electrophotographic sensitive body | JP2674089 | 1989-02-07 | JPH02207266A | 1990-08-16 | KAWAHARA TATSURO |
| PURPOSE: To obtain an electrophotographic sensitive body having high sensitivity and high durability by incorporating a specified compd. CONSTITUTION: A compd. represented by formula I (where Cp is a residue of a coupler) is incorporated. The compd. can easily be produced by allowing m-nitrobenzaldehyde to react with dithiooxamide in N,N-dimethylacetamide under heating and refluxing, diazotizing produced 2,5-bis(3-nitrophenyl) thiazolo[4,5-d]thiazole and coupling the obtd. diazo compd. with the coupler Cp in the presence of alkali. An electrophotographic sensitive body having superior durability and high sensitivity is obtd. COPYRIGHT: (C)1990,JPO&Japio | ||||||
| 233 | JPH0224863B2 - | JP15394480 | 1980-11-04 | JPH0224863B2 | 1990-05-30 | BENNETSUTO JOOJI PUERU |
| 234 | Thienone compound | JP12079588 | 1988-05-19 | JPS63305171A | 1988-12-13 | GIYUNTAA HANZEN; YOHANESU PEETAA DEITSUKUSU; HERUMUUTO RAIHERUTO; MASAHIRO HAYASHI |
| 235 | JPS633909B2 - | JP4445279 | 1979-04-13 | JPS633909B2 | 1988-01-26 | HAINTSU AIRINGUSUFUERUTO; GYUNTAA HANZEN; GYUNTAA ZEIBORUTO; GEORUKU TSUAIDORAA |
| 236 | Electrophotographic sensitive body | JP13817386 | 1986-06-16 | JPS62295060A | 1987-12-22 | AKASAKI YUTAKA; TOKIDA AKIHIKO; TORIGOE KAORU; IMAI AKIRA; ISHII TORU |
| PURPOSE:To enhance sensitivity and durability by incorporating a bisazo compound having a specified type in a photosensitive layer formed on a conductive substrate. CONSTITUTION:The photosensitive layer formed on the conductive substrate contains one of the bisazo compounds represented by formula I in which A is a divalent aromatic hydrocarbon group or divalent heterocyclic group containing N in the ring; X is H or halogen; Cp is a group selected from formulae 1-4; Y is an optionally substituted aromatic carbon ring or the like; Z is optionally substituted carbamoyl or the like; R1 is H, optionally substituted alkyl, or the like; R2 is optionally substituted aryl or the like; and R3 is an optionally substituted aryl, heterocyclic group, or the like, thus permitting the obtained electrophotographic sensitive body to be superior in the pints of sensitivity and durability as compared with the ones using conventional organic photoconductors. | ||||||
| 237 | JPS6248992B2 - | JP899481 | 1981-01-26 | JPS6248992B2 | 1987-10-16 | KAWAMURA KIMIHIDE; HORIGUCHI SHOJIRO |
| 238 | Method of coloring novel transition metal complex and high polymer organic material | JP13065185 | 1985-06-15 | JPS6112756A | 1986-01-21 | GEORUGU CHIEE; PAURU RIINHARUTO |
| 239 | Recording material for electronic photograph and its manufacture | JP4302582 | 1982-03-19 | JPS57176046A | 1982-10-29 | FURITSUTSU GURAASAA; GEERUHARUTO HOFUMAN; RAINHORUTO IYOTSUTO REIRAA; PEETAA NOIMAN; MANFUREETO PACHI |
| 240 | Coloring method of organic material | JP899481 | 1981-01-26 | JPS57123261A | 1982-07-31 | KAWAMURA KIMIHIDE; HORIGUCHI SHIYOUJIROU |
| NEW MATERIAL:Compounds of the formula wherein R 1 is a benzene or naphthalene ring having a hydroxyl group; R 2 is an arom. amine residue. USE: Dyes which dye org. materials, particularly hydrophobic synthetic fibers such as polyester fibers blueWyellowWreddish brown and give dyed materials with good resistance to light and sublimation and fastness. They exhibit good dyeing properties in both high-temperature dyeing and carrier dyeing. PREPARATION: 3,3-Dimethoxy-4,5,6,7-tetrachloroisoindoline-1-one, 3-imino-4,5,6,7- tetrachloroisoindoline-1-one or 3,3,4,5,6,7-hexachloroisoindoline-1-one is reacted with an aminonaphthol or an aminophenol in a molar ratio of 1:1. The resulting coupling component is coupled with a diazo compd. derived from an arom. prim. amine. COPYRIGHT: (C)1982,JPO&Japio | ||||||
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