SPIROOXAZINE DERIVATIVE AND SENSITIZED MATERIAL USING SAID DERIVATIVE

NEW MATERIAL:A compound shown by formula I (n is 1-6; R is alkyl; R and R are >= 2C alkyl, alkoxyalkyl, cycloalkyl or aryl; rings A and B are hydrocarbon aromatic ring or hetetocylic aromatic ring which may be replaced). EXAMPLE:A compound shown by formula II. USE:A photochromic sensitized materi...

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Hauptverfasser:	MAEDA SHUICHI, KIMURA YUKIYO, TATEOKA YASUO
Format:	Patent
Sprache:	eng
Schlagworte:	ADHESIVES AUXILIARY PROCESSES IN PHOTOGRAPHY 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 FREQUENCY-CHANGING HETEROCYCLIC COMPOUNDS HOLOGRAPHY LAKES MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE 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 PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR,STEREO-PHOTOGRAPHIC PROCESSES PHOTOGRAPHY PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES PHYSICS POLISHES TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF
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Beschreibung
Zusammenfassung:	NEW MATERIAL:A compound shown by formula I (n is 1-6; R is alkyl; R and R are >= 2C alkyl, alkoxyalkyl, cycloalkyl or aryl; rings A and B are hydrocarbon aromatic ring or hetetocylic aromatic ring which may be replaced). EXAMPLE:A compound shown by formula II. USE:A photochromic sensitized material usable as light adjusting material, optical filter, masking material and actinometer having improved compatibility with high polymer compound, coloring concentration and fastness to colored state. PREPARATION:For example, an indolenine compound (e.g. 2-methyl-3,3-dimethyl- indolenine, etc.) shown by formula III is reacted with an alkylating agent (e.g. p-toluenesulfonic acid methoxyethyl ester, etc.) shown by formula IV and then with a nitroso-hydroxy derivative shown by formula V.