FLUESSIGKRISTALLINE PHASE

1. Liquid crystal phase consisting of 3 to 25 components, characterised in that it contains 3 to 15 pyrimidine compounds of the formula I R**1 -A**1 -Z**1 -A**2 -R**2 wherein R**1 and R**2 in each case independently of one another are an alkyl or an alkoxy group with up to 12 C atoms, A**1 is -A-, -...

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WEBER,GEORG
description 1. Liquid crystal phase consisting of 3 to 25 components, characterised in that it contains 3 to 15 pyrimidine compounds of the formula I R**1 -A**1 -Z**1 -A**2 -R**2 wherein R**1 and R**2 in each case independently of one another are an alkyl or an alkoxy group with up to 12 C atoms, A**1 is -A-, -A**4 -A- or -A-Z**3 -A**4 -, A is pyrimidine-2,5-diyl, A**2 and A**4 are in each case 1,4-phenylene which is unsubstituted or substituted by one or two F and/or Cl atoms and/or CH3 groups and/or CN groups, it also being possible for one or two CH groups to be replaced by N atoms, 1,4-cyclohexylene, it also being possible for one or two non-adjacent CH2 groups to be replaced by 0 atoms, 1,3-dithiane-2,5-diyl, 1,4-bicyclo(2,2,2)-octylene, decahydronapthaline-2,6-diyl or 1,2,3,4-tetrahydronaphthalene-2,6-diyl, and Z**1 and Z**3 are in each case -CO-O-, -O-CO-, -CH2 CH2 -, -OCH2 -, -CH2 O- or a single bond, these pyrimidine compounds being contained with a total content of 20 to 94%, whereby two pyrimidine compounds of the formula I have four different end group substituents R**1 and R**2 , and the liquid crystal phase further contains other constituents of the formula II R'-L-G-E-R" wherein L and E are each a carbocyclic or heterocyclic ring system from the group formed by 1,4-disubstituted benzene and cyclohexane rings, 4,4'-disubstituted biphenyl, phenylcyclohexane and cyclohexylcyclohexane systems, 2,5-disubstituted 1,3-dioxane rings, 2,6-disubstituted naphthalene, di- and tetra-hydronapthalene, quinazoline and tetrahydroquinazoline, G is -CH=CH- -C-=C- -CH=N- -N(O)=N- -CH=N(O)- -CH2 -CH2 - -CH2 -O- -CH2 -S- or a C-C single bond, and R' and R" are alkyl, alkoxy, alkanoyloxy or alkoxycarbonyloxy with up to 8 carbon atoms, or one of these radicals is also CN, NC, NO2 , CF3 , F, Cl or Br.
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Liquid crystal phase consisting of 3 to 25 components, characterised in that it contains 3 to 15 pyrimidine compounds of the formula I R**1 -A**1 -Z**1 -A**2 -R**2 wherein R**1 and R**2 in each case independently of one another are an alkyl or an alkoxy group with up to 12 C atoms, A**1 is -A-, -A**4 -A- or -A-Z**3 -A**4 -, A is pyrimidine-2,5-diyl, A**2 and A**4 are in each case 1,4-phenylene which is unsubstituted or substituted by one or two F and/or Cl atoms and/or CH3 groups and/or CN groups, it also being possible for one or two CH groups to be replaced by N atoms, 1,4-cyclohexylene, it also being possible for one or two non-adjacent CH2 groups to be replaced by 0 atoms, 1,3-dithiane-2,5-diyl, 1,4-bicyclo(2,2,2)-octylene, decahydronapthaline-2,6-diyl or 1,2,3,4-tetrahydronaphthalene-2,6-diyl, and Z**1 and Z**3 are in each case -CO-O-, -O-CO-, -CH2 CH2 -, -OCH2 -, -CH2 O- or a single bond, these pyrimidine compounds being contained with a total content of 20 to 94%, whereby two pyrimidine compounds of the formula I have four different end group substituents R**1 and R**2 , and the liquid crystal phase further contains other constituents of the formula II R'-L-G-E-R" wherein L and E are each a carbocyclic or heterocyclic ring system from the group formed by 1,4-disubstituted benzene and cyclohexane rings, 4,4'-disubstituted biphenyl, phenylcyclohexane and cyclohexylcyclohexane systems, 2,5-disubstituted 1,3-dioxane rings, 2,6-disubstituted naphthalene, di- and tetra-hydronapthalene, quinazoline and tetrahydroquinazoline, G is -CH=CH- -C-=C- -CH=N- -N(O)=N- -CH=N(O)- -CH2 -CH2 - -CH2 -O- -CH2 -S- or a C-C single bond, and R' and R" are alkyl, alkoxy, alkanoyloxy or alkoxycarbonyloxy with up to 8 carbon atoms, or one of these radicals is also CN, NC, NO2 , CF3 , F, Cl or Br.</description><edition>4</edition><language>ger</language><subject>ADHESIVES ; CHEMISTRY ; 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 ; FREQUENCY-CHANGING ; MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; NATURAL RESINS ; NON-LINEAR OPTICS ; OPTICAL ANALOGUE/DIGITAL CONVERTERS ; OPTICAL LOGIC ELEMENTS ; OPTICS ; PAINTS ; PHYSICS ; POLISHES ; TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF</subject><creationdate>1985</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&amp;date=19850808&amp;DB=EPODOC&amp;CC=DE&amp;NR=3404117A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19850808&amp;DB=EPODOC&amp;CC=DE&amp;NR=3404117A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SCHEUBLE,BERNHARD,.DR</creatorcontrib><creatorcontrib>WEBER,GEORG</creatorcontrib><title>FLUESSIGKRISTALLINE PHASE</title><description>1. Liquid crystal phase consisting of 3 to 25 components, characterised in that it contains 3 to 15 pyrimidine compounds of the formula I R**1 -A**1 -Z**1 -A**2 -R**2 wherein R**1 and R**2 in each case independently of one another are an alkyl or an alkoxy group with up to 12 C atoms, A**1 is -A-, -A**4 -A- or -A-Z**3 -A**4 -, A is pyrimidine-2,5-diyl, A**2 and A**4 are in each case 1,4-phenylene which is unsubstituted or substituted by one or two F and/or Cl atoms and/or CH3 groups and/or CN groups, it also being possible for one or two CH groups to be replaced by N atoms, 1,4-cyclohexylene, it also being possible for one or two non-adjacent CH2 groups to be replaced by 0 atoms, 1,3-dithiane-2,5-diyl, 1,4-bicyclo(2,2,2)-octylene, decahydronapthaline-2,6-diyl or 1,2,3,4-tetrahydronaphthalene-2,6-diyl, and Z**1 and Z**3 are in each case -CO-O-, -O-CO-, -CH2 CH2 -, -OCH2 -, -CH2 O- or a single bond, these pyrimidine compounds being contained with a total content of 20 to 94%, whereby two pyrimidine compounds of the formula I have four different end group substituents R**1 and R**2 , and the liquid crystal phase further contains other constituents of the formula II R'-L-G-E-R" wherein L and E are each a carbocyclic or heterocyclic ring system from the group formed by 1,4-disubstituted benzene and cyclohexane rings, 4,4'-disubstituted biphenyl, phenylcyclohexane and cyclohexylcyclohexane systems, 2,5-disubstituted 1,3-dioxane rings, 2,6-disubstituted naphthalene, di- and tetra-hydronapthalene, quinazoline and tetrahydroquinazoline, G is -CH=CH- -C-=C- -CH=N- -N(O)=N- -CH=N(O)- -CH2 -CH2 - -CH2 -O- -CH2 -S- or a C-C single bond, and R' and R" are alkyl, alkoxy, alkanoyloxy or alkoxycarbonyloxy with up to 8 carbon atoms, or one of these radicals is also CN, NC, NO2 , CF3 , F, Cl or Br.</description><subject>ADHESIVES</subject><subject>CHEMISTRY</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>FREQUENCY-CHANGING</subject><subject>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</subject><subject>METALLURGY</subject><subject>MISCELLANEOUS APPLICATIONS OF MATERIALS</subject><subject>MISCELLANEOUS COMPOSITIONS</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>PAINTS</subject><subject>PHYSICS</subject><subject>POLISHES</subject><subject>TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1985</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJB08wl1DQ72dPcO8gwOcfTx8fRzVQjwcAx25WFgTUvMKU7lhdLcDApuriHOHrqpBfnxqcUFicmpeakl8S6uxiYGJoaG5o6GxkQoAQDsax-t</recordid><startdate>19850808</startdate><enddate>19850808</enddate><creator>SCHEUBLE,BERNHARD,.DR</creator><creator>WEBER,GEORG</creator><scope>EVB</scope></search><sort><creationdate>19850808</creationdate><title>FLUESSIGKRISTALLINE PHASE</title><author>SCHEUBLE,BERNHARD,.DR ; WEBER,GEORG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE3404117A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1985</creationdate><topic>ADHESIVES</topic><topic>CHEMISTRY</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>FREQUENCY-CHANGING</topic><topic>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</topic><topic>METALLURGY</topic><topic>MISCELLANEOUS APPLICATIONS OF MATERIALS</topic><topic>MISCELLANEOUS COMPOSITIONS</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>PAINTS</topic><topic>PHYSICS</topic><topic>POLISHES</topic><topic>TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF</topic><toplevel>online_resources</toplevel><creatorcontrib>SCHEUBLE,BERNHARD,.DR</creatorcontrib><creatorcontrib>WEBER,GEORG</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>SCHEUBLE,BERNHARD,.DR</au><au>WEBER,GEORG</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>FLUESSIGKRISTALLINE PHASE</title><date>1985-08-08</date><risdate>1985</risdate><abstract>1. Liquid crystal phase consisting of 3 to 25 components, characterised in that it contains 3 to 15 pyrimidine compounds of the formula I R**1 -A**1 -Z**1 -A**2 -R**2 wherein R**1 and R**2 in each case independently of one another are an alkyl or an alkoxy group with up to 12 C atoms, A**1 is -A-, -A**4 -A- or -A-Z**3 -A**4 -, A is pyrimidine-2,5-diyl, A**2 and A**4 are in each case 1,4-phenylene which is unsubstituted or substituted by one or two F and/or Cl atoms and/or CH3 groups and/or CN groups, it also being possible for one or two CH groups to be replaced by N atoms, 1,4-cyclohexylene, it also being possible for one or two non-adjacent CH2 groups to be replaced by 0 atoms, 1,3-dithiane-2,5-diyl, 1,4-bicyclo(2,2,2)-octylene, decahydronapthaline-2,6-diyl or 1,2,3,4-tetrahydronaphthalene-2,6-diyl, and Z**1 and Z**3 are in each case -CO-O-, -O-CO-, -CH2 CH2 -, -OCH2 -, -CH2 O- or a single bond, these pyrimidine compounds being contained with a total content of 20 to 94%, whereby two pyrimidine compounds of the formula I have four different end group substituents R**1 and R**2 , and the liquid crystal phase further contains other constituents of the formula II R'-L-G-E-R" wherein L and E are each a carbocyclic or heterocyclic ring system from the group formed by 1,4-disubstituted benzene and cyclohexane rings, 4,4'-disubstituted biphenyl, phenylcyclohexane and cyclohexylcyclohexane systems, 2,5-disubstituted 1,3-dioxane rings, 2,6-disubstituted naphthalene, di- and tetra-hydronapthalene, quinazoline and tetrahydroquinazoline, G is -CH=CH- -C-=C- -CH=N- -N(O)=N- -CH=N(O)- -CH2 -CH2 - -CH2 -O- -CH2 -S- or a C-C single bond, and R' and R" are alkyl, alkoxy, alkanoyloxy or alkoxycarbonyloxy with up to 8 carbon atoms, or one of these radicals is also CN, NC, NO2 , CF3 , F, Cl or Br.</abstract><edition>4</edition><oa>free_for_read</oa></addata></record>
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subjects ADHESIVES
CHEMISTRY
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
FREQUENCY-CHANGING
MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE
METALLURGY
MISCELLANEOUS APPLICATIONS OF MATERIALS
MISCELLANEOUS COMPOSITIONS
NATURAL RESINS
NON-LINEAR OPTICS
OPTICAL ANALOGUE/DIGITAL CONVERTERS
OPTICAL LOGIC ELEMENTS
OPTICS
PAINTS
PHYSICS
POLISHES
TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF
title FLUESSIGKRISTALLINE PHASE
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