Chromophoric compounds and their preparation process

New chromophore compounds are 7-aminophenoxazines (I) with a condensed carbo- or heterocyclic ring substituted by an electron acceptor-substituted methylene or imino group. New chromophore compounds are 7-aminophenoxazines, with a condensed carbo- or heterocyclic ring substituted by an electron acce...

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Bibliographische Detailangaben
Hauptverfasser:	HARTMANN, HORST DR, KANITZ, ANDREAS DR, FRICKE, CHRISTIAN DR
Format:	Patent
Sprache:	eng ; fre ; ger
Schlagworte:	ADHESIVES CHEMISTRY CINEMATOGRAPHY DEVICES OR ARRANGEMENTS, THE OPTICAL OPERATION OF WHICH ISMODIFIED BY CHANGING THE OPTICAL PROPERTIES OF THE MEDIUM OF THEDEVICES OR ARRANGEMENTS FOR THE CONTROL OF THE INTENSITY,COLOUR, PHASE, POLARISATION OR DIRECTION OF LIGHT, e.g.SWITCHING, GATING, MODULATING OR DEMODULATING DYES ELECTROGRAPHY ELECTROPHOTOGRAPHY FREQUENCY-CHANGING HETEROCYCLIC COMPOUNDS HOLOGRAPHY LAKES MAGNETOGRAPHY METALLURGY MISCELLANEOUS APPLICATIONS OF MATERIALS MISCELLANEOUS COMPOSITIONS MORDANTS NATURAL RESINS NON-LINEAR OPTICS OPTICAL ANALOGUE/DIGITAL CONVERTERS OPTICAL LOGIC ELEMENTS OPTICS ORGANIC CHEMISTRY ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES PAINTS PHOTOGRAPHY PHYSICS POLISHES TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF
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Beschreibung
Zusammenfassung:	New chromophore compounds are 7-aminophenoxazines (I) with a condensed carbo- or heterocyclic ring substituted by an electron acceptor-substituted methylene or imino group. New chromophore compounds are 7-aminophenoxazines, with a condensed carbo- or heterocyclic ring substituted by an electron acceptor-substituted methylene or imino group, of formula (I); R , R , R , R , R = hydrogen (I), linear or branched 1-20 carbon (C) alkyl (optionally with 1-5 ether oxygen (O) atoms in the chain), aryl or heteroaryl; R , R can also = benzyl; or one of R , R = is hydroxyl (OH) or carboxyl; Z = an electron acceptor-substituted methylene or imino group; X = sulfur (S), O, NR , a ring double bond or a (hetero)cyclic group of formula (II): ; T = CH or N; or optionally Z and T together = a structure of the type =N-SO2-C=, =N-CS-C= or =N-CO-C=; Y = CR or N; R , R = H, linear or branched 1-20 C alkyl, phenyl or naphthyl. An Independent claim is also included for the preparation of (I).