Monophasic solid solutions with asymmetrical pyrrolo-(4-3-c)-pyrroles as host

Uni-phase solid solutions comprise 60-90 mole-% asymmetric 2, 5-dihydro-1, 4-diketopyrroloÄ3, 4-cÜpyrrole of formula (I) and 40-10 mole-% 2, 5-dihydro-1, 4-diketopyrroloÄ3, 4-cÜpyrrole of formula (IIa) or quinacridone of formula (IIb). G1, G2 = unsubstituted phenyl, 3- or 4-pyridyl or naphthyl, or a...

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Hauptverfasser: HAO, ZHIMIN, IQBAL, ABUL
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IQBAL, ABUL
description Uni-phase solid solutions comprise 60-90 mole-% asymmetric 2, 5-dihydro-1, 4-diketopyrroloÄ3, 4-cÜpyrrole of formula (I) and 40-10 mole-% 2, 5-dihydro-1, 4-diketopyrroloÄ3, 4-cÜpyrrole of formula (IIa) or quinacridone of formula (IIb). G1, G2 = unsubstituted phenyl, 3- or 4-pyridyl or naphthyl, or a group of formula (IIIa-IIIe); in which R1, R2 = F, Cl, Br, CN, NO2, CF3, 1-8 C alkyl, 5-6 C cycloalkyl, phenyl, 1-8 C alkoxy(carbonyl), mono- or di-(1-8 C alkyl)amino(carbonyl) or morpholino; R3 = -O-, -NR5-, -N=N- or -SO2-; R4 = H, F, Cl, Br, CN, NO2, CF3, 1-8 C alkyl, 1-8 C alkoxy(carbonyl) or mono- or di-(1-8 C alkyl)-amino(carbonyl); R5 = H, Me or Et; or but if one of G1 and G2 = unsubstituted phenyl or 3- or 4-pyridyl, the other is not unsubstituted phenyl, 3- or 4-pyridyl or a (IIIa) or (IIIb) group with (a) R2 = Cl and R1 = H, F or CF3, (b) R1 = Cl and R2 = F or CF3 or (c) R1, R2 = F, M e or CF3; G3, G4 = an unsubstituted phenyl or 3- or 4-pyridyl group or a group of formula (IIIa) or (IIIb) in which R1, R2 = F, Cl, CN, NO2, CF3, 1-4 C alkyl, 1-4 C alkoxy or mono- or di-(1-4 C alkyl)-amino; R9 = H, halogen, 1-4 C alkyl or 1-4 C alkoxy. Also claimed is a composition containing the solid solution and a high molecular organic material. Preferably the solid solution contains 75-90, especially 75-84 mole-% (I) and 25-10, especially 25-16 mole-% (IIa) or (IIb). It may be subjected to thermal treatment or recrystallised after it has been prepd.
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G1, G2 = unsubstituted phenyl, 3- or 4-pyridyl or naphthyl, or a group of formula (IIIa-IIIe); in which R1, R2 = F, Cl, Br, CN, NO2, CF3, 1-8 C alkyl, 5-6 C cycloalkyl, phenyl, 1-8 C alkoxy(carbonyl), mono- or di-(1-8 C alkyl)amino(carbonyl) or morpholino; R3 = -O-, -NR5-, -N=N- or -SO2-; R4 = H, F, Cl, Br, CN, NO2, CF3, 1-8 C alkyl, 1-8 C alkoxy(carbonyl) or mono- or di-(1-8 C alkyl)-amino(carbonyl); R5 = H, Me or Et; or but if one of G1 and G2 = unsubstituted phenyl or 3- or 4-pyridyl, the other is not unsubstituted phenyl, 3- or 4-pyridyl or a (IIIa) or (IIIb) group with (a) R2 = Cl and R1 = H, F or CF3, (b) R1 = Cl and R2 = F or CF3 or (c) R1, R2 = F, M e or CF3; G3, G4 = an unsubstituted phenyl or 3- or 4-pyridyl group or a group of formula (IIIa) or (IIIb) in which R1, R2 = F, Cl, CN, NO2, CF3, 1-4 C alkyl, 1-4 C alkoxy or mono- or di-(1-4 C alkyl)-amino; R9 = H, halogen, 1-4 C alkyl or 1-4 C alkoxy. Also claimed is a composition containing the solid solution and a high molecular organic material. Preferably the solid solution contains 75-90, especially 75-84 mole-% (I) and 25-10, especially 25-16 mole-% (IIa) or (IIb). It may be subjected to thermal treatment or recrystallised after it has been prepd.</description><edition>7</edition><language>eng ; fre ; ger</language><subject>ADHESIVES ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; COMPOSITIONS OF MACROMOLECULAR COMPOUNDS ; DYES ; HETEROCYCLIC COMPOUNDS ; LAKES ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; MORDANTS ; NATURAL RESINS ; ORGANIC CHEMISTRY ; ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES ; ORGANIC MACROMOLECULAR COMPOUNDS ; PAINTS ; POLISHES ; THEIR PREPARATION OR CHEMICAL WORKING-UP ; USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS</subject><creationdate>2001</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=20010221&amp;DB=EPODOC&amp;CC=EP&amp;NR=0765919B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25562,76317</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20010221&amp;DB=EPODOC&amp;CC=EP&amp;NR=0765919B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HAO, ZHIMIN</creatorcontrib><creatorcontrib>IQBAL, ABUL</creatorcontrib><title>Monophasic solid solutions with asymmetrical pyrrolo-(4-3-c)-pyrroles as host</title><description>Uni-phase solid solutions comprise 60-90 mole-% asymmetric 2, 5-dihydro-1, 4-diketopyrroloÄ3, 4-cÜpyrrole of formula (I) and 40-10 mole-% 2, 5-dihydro-1, 4-diketopyrroloÄ3, 4-cÜpyrrole of formula (IIa) or quinacridone of formula (IIb). G1, G2 = unsubstituted phenyl, 3- or 4-pyridyl or naphthyl, or a group of formula (IIIa-IIIe); in which R1, R2 = F, Cl, Br, CN, NO2, CF3, 1-8 C alkyl, 5-6 C cycloalkyl, phenyl, 1-8 C alkoxy(carbonyl), mono- or di-(1-8 C alkyl)amino(carbonyl) or morpholino; R3 = -O-, -NR5-, -N=N- or -SO2-; R4 = H, F, Cl, Br, CN, NO2, CF3, 1-8 C alkyl, 1-8 C alkoxy(carbonyl) or mono- or di-(1-8 C alkyl)-amino(carbonyl); R5 = H, Me or Et; or but if one of G1 and G2 = unsubstituted phenyl or 3- or 4-pyridyl, the other is not unsubstituted phenyl, 3- or 4-pyridyl or a (IIIa) or (IIIb) group with (a) R2 = Cl and R1 = H, F or CF3, (b) R1 = Cl and R2 = F or CF3 or (c) R1, R2 = F, M e or CF3; G3, G4 = an unsubstituted phenyl or 3- or 4-pyridyl group or a group of formula (IIIa) or (IIIb) in which R1, R2 = F, Cl, CN, NO2, CF3, 1-4 C alkyl, 1-4 C alkoxy or mono- or di-(1-4 C alkyl)-amino; R9 = H, halogen, 1-4 C alkyl or 1-4 C alkoxy. Also claimed is a composition containing the solid solution and a high molecular organic material. Preferably the solid solution contains 75-90, especially 75-84 mole-% (I) and 25-10, especially 25-16 mole-% (IIa) or (IIb). 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G1, G2 = unsubstituted phenyl, 3- or 4-pyridyl or naphthyl, or a group of formula (IIIa-IIIe); in which R1, R2 = F, Cl, Br, CN, NO2, CF3, 1-8 C alkyl, 5-6 C cycloalkyl, phenyl, 1-8 C alkoxy(carbonyl), mono- or di-(1-8 C alkyl)amino(carbonyl) or morpholino; R3 = -O-, -NR5-, -N=N- or -SO2-; R4 = H, F, Cl, Br, CN, NO2, CF3, 1-8 C alkyl, 1-8 C alkoxy(carbonyl) or mono- or di-(1-8 C alkyl)-amino(carbonyl); R5 = H, Me or Et; or but if one of G1 and G2 = unsubstituted phenyl or 3- or 4-pyridyl, the other is not unsubstituted phenyl, 3- or 4-pyridyl or a (IIIa) or (IIIb) group with (a) R2 = Cl and R1 = H, F or CF3, (b) R1 = Cl and R2 = F or CF3 or (c) R1, R2 = F, M e or CF3; G3, G4 = an unsubstituted phenyl or 3- or 4-pyridyl group or a group of formula (IIIa) or (IIIb) in which R1, R2 = F, Cl, CN, NO2, CF3, 1-4 C alkyl, 1-4 C alkoxy or mono- or di-(1-4 C alkyl)-amino; R9 = H, halogen, 1-4 C alkyl or 1-4 C alkoxy. Also claimed is a composition containing the solid solution and a high molecular organic material. Preferably the solid solution contains 75-90, especially 75-84 mole-% (I) and 25-10, especially 25-16 mole-% (IIa) or (IIb). It may be subjected to thermal treatment or recrystallised after it has been prepd.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record>
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subjects ADHESIVES
CHEMISTRY
COMPOSITIONS BASED THEREON
COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
DYES
HETEROCYCLIC COMPOUNDS
LAKES
METALLURGY
MISCELLANEOUS APPLICATIONS OF MATERIALS
MISCELLANEOUS COMPOSITIONS
MORDANTS
NATURAL RESINS
ORGANIC CHEMISTRY
ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES
ORGANIC MACROMOLECULAR COMPOUNDS
PAINTS
POLISHES
THEIR PREPARATION OR CHEMICAL WORKING-UP
USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS
title Monophasic solid solutions with asymmetrical pyrrolo-(4-3-c)-pyrroles as host
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