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序号	专利名	申请号	申请日	公开（公告）号	公开（公告）日	发明人
121	CHROMIUM COMPLEX DYES	GB8511629	1985-05-08	GB2158451A	1985-11-13	SCHLESINGER ULRICH; BEFFA FABIO

122	Chromium or cobalt complexes, their preparation and use	DE3512253	1985-04-03	DE3512253A1	1985-10-17	BACK GERHARD DR
The invention relates to chromium or cobalt complexes of the formula in which A is the radical of a dicyclic metallisable azo or azomethine dye, B is the radical of a tridentate, dianionic, complex-forming organic compound, which contains an group participating in the chromium or cobalt complex, Me is a chromium or cobalt atom and Ka is a cation, a process for the preparation of the chromium or cobalt complexes of the formula (1) and their use for dyeing.
123	FIBRE-REACTIVE CHROMIUM OR COBALT COMPLEXES	AU4084785	1985-04-04	AU4084785A	1985-10-10	BACK GERHARD; SCHUTZ HANS ULRICH; SCHLESINGER ULRICH

124	Mixtures of 1: 2 chromium complex dyestuffs	DE3409082	1984-03-13	DE3409082A1	1985-09-19	MENNICKE WINFRIED DR; WESTPHAL JOCHEN DR

125	metal complex dyes, their preparation and their uses	FR7822699	1978-08-01	FR2399466B1	1985-06-28

126	DE2529798C2 -	DE2529798	1975-07-03	DE2529798C2	1985-06-20	BACK, GERHARD, DR., 7850 LOERRACH, DE; BEFFA, FABIO, DR., RIEHEN, CH; BUEHLER, ARTHUR, DR., RHEINFELDEN, CH

127	DE2531443C2 -	DE2531443	1975-07-14	DE2531443C2	1985-02-14	BUEHLER, ARTHUR, DR., RHEINFELDEN, CH; SCHUETZ, ULRICH, BASEL, CH

128	FR2411219B1 -	FR7833522	1978-11-28	FR2411219B1	1983-09-23

129		ES510634	1982-03-22	ES510634A0	1983-08-01

130	NICKEL COMPLEX PIGMENTS OF AZINES	CA352411	1980-05-21	CA1146562A	1983-05-17	IQBAL ABUL; LIENHARD PAUL; PUGIN ANDRE
1:1 Nickel complexes of azines of the formula I or of a tautomer thereof (I) wherein R1 is hydrogen or methyl, R2 is methyl or carbamoyl, R3 is hydrogen or chlorine, R4 is hydrogen, chlorine, methyl, trifluoromethyl or sulfamoyl, R5 is hydrogen or chlorine, R6 is hydrogen, chlorine, bromine, methyl, methoxy, trifluoromethyl, carbamoyl or alkanoylamino containing 2 to 4 carbon atoms, with the proviso that, if R2 is carbamoyl, at least two of the substituents R3 to R6 are halogen atoms and/or trifluoromethyl groups, color plastics, lacquers and printing inks in orange to red shades of outstanding fastness properties.
131	A process for dyeing synthetic fiber sauermodifzierten	DE3102316	1981-01-24	DE3102316A1	1982-08-19	FOPPE REIMUND; RAUE RODERICH DR; KUEHLTHAU HANS-PETER DR

132	METAL COMPLEX COMPOUNDS, PROCESS FOR THEIR MANUFACTURE AND THEIR USE AS PIGMENTS	CA308186	1978-07-26	CA1107738A	1981-08-25	TAPPE HORST
Metal complex compounds of formula I wherein X stands for , , or and the benzene or naphthalene ring formed by X and the remaining portion of the molecule may also be substituted with one or two methyl, methoxy, chloro, bromo, trifluoromethyl, nitro, cyano, -CONR1H2 or -COOR3 substituents, R1 and R2 standing for hydrogen or alkyl with 1 to 4 carbon atoms, and R3 for alkyl with 1 to 4 carbon atoms, and Me denotes a nickel, copper, zinc or cobalt atom, are prepared by condensing 3-formyl-4-methyl-2,6-dihydroxy-pyridine or an alkali or alkaline-earth metal salt thereof with an orthoaminohydroxy or compound of formula III (III) The metal complex compounds of formula I are used as pigments, especially for pigmenting lacquers and varnishes.
133	FR2399461B3 -	FR7822811	1978-08-02	FR2399461B3	1981-03-27

134	2-QUINOLONE AZOMETHINE COPPER COMPLEX PIGMENTS	CA281603	1977-06-28	CA1092121A	1980-12-23	CHAMBERLAIN TERENCE R; CAMPBELL COLIN D; MCCRAE JAMES M
A compound having the formula or I IA wherein A denotes an optionally substituted aromatic, isocyclic or heterocyclic residue; R is H, an alkyl residue having from 1 to 6 carbon atoms, an aryl residue having from 6 to 10 carbon atoms or an aralkyl residue having from 7 to 10 carbon atoms; Q is H or a methyl group; X and Y are the same or different and each is a non-water solublising group, or X and Y together form a fused aromatic ring system; and R1 and R2 are the same or different and each is H or an alkyl radical having from 1 to 22 carbon atoms, and R3 is hydrogen, an alkyl radical having from 1 to 22 carbon atoms or an aryl radical having from 6 to 10 carbon atoms, the alkyl radicals in R1, R2 and R3 being unsubstituted and uninterrupted or being substituted by an OH, NH2, or CN group and/or being interrupted by an ethylenic group or an oxygen, sulphur or nitrogen bridge, or two or all three of R1, R2 and R3 may form, together with the nitrogen atom to which they are attached a heterocyclic residue, is useful for pigmenting high molecular weight organic material.
135	Method for the coloring of artificial or synthetic materials	FR7901329	1979-01-19	FR2446851A1	1980-08-14	RAU MANFRED
<P>L'invention concerne la coloration des matières artificielles ou synthétiques. </P><P>On utilise comme colorant de dispersion un composé de formule générale :</P>
136	WATER-SOLUBLE 1:2-COBALT COMPLEX DYESTUFFS	AU2454477	1977-04-22	AU509686B2	1980-05-22	FUCHS H; FILZINGER K

137	CHROMIUM COMPLEXES	AU1392076	1976-05-13	AU508949B2	1980-04-17	BEFFA F; BACK G; STEINER E

138	AZOMETHINE DYES FOR POLYPROPYLENE	CA260351	1976-09-01	CA1068684A	1979-12-25	BOTROS RAOUF
Azomethine dyes of the formula in which A represents a diazotizable aromatic hydrocarbon. In particular, A is an optionally substituted benzene or naphthalene radical. B is an optionally substituted salicylaldehyde or o-hydroxy-naphthaldehyde nucleus and C is an optionally substituted pyridine nucleus. Metal-modified polypropylene dyed with the azomethine dye has excellent fastness properties.
139	BISAZOMETHINE DYES FOR POLYPROPYLENE	CA260350	1976-09-01	CA1068682A	1979-12-25	BOTROS RAOUF
Bizazomethine dyes of the general formula: in which A and D are optionally substituted benzene or naphthalene nuclei, E is an optionally substituted salicyaldehyde or o-hydroxy-naphthaladehyde nucleus and G is an optionally substituted 2-amino-pyridine nucleus. Metal-modified polypropylene dyed with the bisazomethine dye has excellent fastness properties.
140		IT5050575	1975-07-14	IT1040931B	1979-12-20

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