Chromophoric compounds and their preparation process
Chromophore, NLO-aktive Verbindungen der allgemeinen Formel 1 und Verfahren zur Herstellung solcher Verbindungen. Die erfindungsgemäßen Verbindungen können zur Herstellung von NLO-aktiven Polymeren und damit zum Aufbau von elektrooptischen und photonischen Bauelementen verwendet werden. New chromoph...
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| creator | HARTMANN, HORST DR KANITZ, ANDREAS DR FRICKE, CHRISTIAN DR |
| description | Chromophore, NLO-aktive Verbindungen der allgemeinen Formel 1 und Verfahren zur Herstellung solcher Verbindungen. Die erfindungsgemäßen Verbindungen können zur Herstellung von NLO-aktiven Polymeren und damit zum Aufbau von elektrooptischen und photonischen Bauelementen verwendet werden.
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). |
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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).</description><edition>6</edition><language>eng ; fre ; ger</language><subject>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</subject><creationdate>1999</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19990922&DB=EPODOC&CC=EP&NR=0943661A2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19990922&DB=EPODOC&CC=EP&NR=0943661A2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HARTMANN, HORST DR</creatorcontrib><creatorcontrib>KANITZ, ANDREAS DR</creatorcontrib><creatorcontrib>FRICKE, CHRISTIAN DR</creatorcontrib><title>Chromophoric compounds and their preparation process</title><description>Chromophore, NLO-aktive Verbindungen der allgemeinen Formel 1 und Verfahren zur Herstellung solcher Verbindungen. Die erfindungsgemäßen Verbindungen können zur Herstellung von NLO-aktiven Polymeren und damit zum Aufbau von elektrooptischen und photonischen Bauelementen verwendet werden.
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).</description><subject>ADHESIVES</subject><subject>CHEMISTRY</subject><subject>CINEMATOGRAPHY</subject><subject>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</subject><subject>DYES</subject><subject>ELECTROGRAPHY</subject><subject>ELECTROPHOTOGRAPHY</subject><subject>FREQUENCY-CHANGING</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HOLOGRAPHY</subject><subject>LAKES</subject><subject>MAGNETOGRAPHY</subject><subject>METALLURGY</subject><subject>MISCELLANEOUS APPLICATIONS OF MATERIALS</subject><subject>MISCELLANEOUS COMPOSITIONS</subject><subject>MORDANTS</subject><subject>NATURAL RESINS</subject><subject>NON-LINEAR OPTICS</subject><subject>OPTICAL ANALOGUE/DIGITAL CONVERTERS</subject><subject>OPTICAL LOGIC ELEMENTS</subject><subject>OPTICS</subject><subject>ORGANIC CHEMISTRY</subject><subject>ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES</subject><subject>PAINTS</subject><subject>PHOTOGRAPHY</subject><subject>PHYSICS</subject><subject>POLISHES</subject><subject>TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1999</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDBxzijKz80vyMgvykxWSM7PLcgvzUspVkjMS1EoyUjNLFIoKEotSCxKLMnMzwOy85NTi4t5GFjTEnOKU3mhNDeDgptriLOHbmpBfnxqcUFicmpeakm8a4CBpYmxmZmho5ExEUoAJzUtFw</recordid><startdate>19990922</startdate><enddate>19990922</enddate><creator>HARTMANN, HORST DR</creator><creator>KANITZ, ANDREAS DR</creator><creator>FRICKE, CHRISTIAN DR</creator><scope>EVB</scope></search><sort><creationdate>19990922</creationdate><title>Chromophoric compounds and their preparation process</title><author>HARTMANN, HORST DR ; KANITZ, ANDREAS DR ; FRICKE, CHRISTIAN DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_EP0943661A23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre ; ger</language><creationdate>1999</creationdate><topic>ADHESIVES</topic><topic>CHEMISTRY</topic><topic>CINEMATOGRAPHY</topic><topic>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</topic><topic>DYES</topic><topic>ELECTROGRAPHY</topic><topic>ELECTROPHOTOGRAPHY</topic><topic>FREQUENCY-CHANGING</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HOLOGRAPHY</topic><topic>LAKES</topic><topic>MAGNETOGRAPHY</topic><topic>METALLURGY</topic><topic>MISCELLANEOUS APPLICATIONS OF MATERIALS</topic><topic>MISCELLANEOUS COMPOSITIONS</topic><topic>MORDANTS</topic><topic>NATURAL RESINS</topic><topic>NON-LINEAR OPTICS</topic><topic>OPTICAL ANALOGUE/DIGITAL CONVERTERS</topic><topic>OPTICAL LOGIC ELEMENTS</topic><topic>OPTICS</topic><topic>ORGANIC CHEMISTRY</topic><topic>ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES</topic><topic>PAINTS</topic><topic>PHOTOGRAPHY</topic><topic>PHYSICS</topic><topic>POLISHES</topic><topic>TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF</topic><toplevel>online_resources</toplevel><creatorcontrib>HARTMANN, HORST DR</creatorcontrib><creatorcontrib>KANITZ, ANDREAS DR</creatorcontrib><creatorcontrib>FRICKE, CHRISTIAN DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>HARTMANN, HORST DR</au><au>KANITZ, ANDREAS DR</au><au>FRICKE, CHRISTIAN DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Chromophoric compounds and their preparation process</title><date>1999-09-22</date><risdate>1999</risdate><abstract>Chromophore, NLO-aktive Verbindungen der allgemeinen Formel 1 und Verfahren zur Herstellung solcher Verbindungen. Die erfindungsgemäßen Verbindungen können zur Herstellung von NLO-aktiven Polymeren und damit zum Aufbau von elektrooptischen und photonischen Bauelementen verwendet werden.
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).</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
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| subjects | 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 |
| title | Chromophoric compounds and their preparation process |
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