Liquid-crystalline polyimides, 23Part 22: H. R. Kricheldorf, M. Gurau, J. Macromol. Sci., Pure Appl. Chem., in press. Photoreactive, cholesteric copoly(ester-imide)s derived from 1,4-phenylenediacrylic acid and 4-aminobenzoic trimellitimide
The dichlorides of commercial 1,4-phenylenediacrylic acid3,3′-(1,4-Phenylene)di-2-propenoic acid. and N-(4-carboxyphenyl)-trimellitimide were polycondensed with a chiral spacer prepared from (S)-3-bromo-2-methylpropanol and 4-mercaptophenol. Optical microscopy revealed that all the resulting copoly(...
Ausführliche Beschreibung
Gespeichert in:
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E-Artikel |
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Englisch |
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1995 |
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8 Ill. ; 2 Tab. 13 |
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Wiley InterScience Backfile Collection 1832-2000 |
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in: Macromolecular Chemistry and Physics - Weinheim : Wiley-VCH, 196(1995) vom: Nov., Seite 3511-3523 |
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volume:196 ; year:1995 ; month:11 ; pages:3511-3523 ; extent:13 |
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(DE-627)NLEJ163460159 DE-627 ger DE-627 rakwb eng Liquid-crystalline polyimides, 23Part 22: H. R. Kricheldorf, M. Gurau, J. Macromol. Sci., Pure Appl. Chem., in press. Photoreactive, cholesteric copoly(ester-imide)s derived from 1,4-phenylenediacrylic acid and 4-aminobenzoic trimellitimide 1995 8 Ill. 2 Tab. 13 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The dichlorides of commercial 1,4-phenylenediacrylic acid3,3′-(1,4-Phenylene)di-2-propenoic acid. and N-(4-carboxyphenyl)-trimellitimide were polycondensed with a chiral spacer prepared from (S)-3-bromo-2-methylpropanol and 4-mercaptophenol. Optical microscopy revealed that all the resulting copoly(ester-imide)s form an enantiotropic cholesteric melt and adopt a Grandjean texture upon slight shearing. The WAXD powder patterns indicate the formation of a layered structure in the solid state. Irradiation with UV light of wavelength ≤ 360 nm allows crosslinking at any temperature above 25°C. Wiley InterScience Backfile Collection 1832-2000 Kricheldorf, Hans R. oth Probst, Nicolas oth in Macromolecular Chemistry and Physics Weinheim : Wiley-VCH 196(1995) vom: Nov., Seite 3511-3523 (DE-627)NLEJ159071399 (DE-600)1475026-0 1022-1352 nnns volume:196 year:1995 month:11 pages:3511-3523 extent:13 http://dx.doi.org/10.1002/macp.1995.021961106 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 196 1995 11 3511-3523 13 |
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(DE-627)NLEJ163460159 DE-627 ger DE-627 rakwb eng Liquid-crystalline polyimides, 23Part 22: H. R. Kricheldorf, M. Gurau, J. Macromol. Sci., Pure Appl. Chem., in press. Photoreactive, cholesteric copoly(ester-imide)s derived from 1,4-phenylenediacrylic acid and 4-aminobenzoic trimellitimide 1995 8 Ill. 2 Tab. 13 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The dichlorides of commercial 1,4-phenylenediacrylic acid3,3′-(1,4-Phenylene)di-2-propenoic acid. and N-(4-carboxyphenyl)-trimellitimide were polycondensed with a chiral spacer prepared from (S)-3-bromo-2-methylpropanol and 4-mercaptophenol. Optical microscopy revealed that all the resulting copoly(ester-imide)s form an enantiotropic cholesteric melt and adopt a Grandjean texture upon slight shearing. The WAXD powder patterns indicate the formation of a layered structure in the solid state. Irradiation with UV light of wavelength ≤ 360 nm allows crosslinking at any temperature above 25°C. Wiley InterScience Backfile Collection 1832-2000 Kricheldorf, Hans R. oth Probst, Nicolas oth in Macromolecular Chemistry and Physics Weinheim : Wiley-VCH 196(1995) vom: Nov., Seite 3511-3523 (DE-627)NLEJ159071399 (DE-600)1475026-0 1022-1352 nnns volume:196 year:1995 month:11 pages:3511-3523 extent:13 http://dx.doi.org/10.1002/macp.1995.021961106 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 196 1995 11 3511-3523 13 |
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(DE-627)NLEJ163460159 DE-627 ger DE-627 rakwb eng Liquid-crystalline polyimides, 23Part 22: H. R. Kricheldorf, M. Gurau, J. Macromol. Sci., Pure Appl. Chem., in press. Photoreactive, cholesteric copoly(ester-imide)s derived from 1,4-phenylenediacrylic acid and 4-aminobenzoic trimellitimide 1995 8 Ill. 2 Tab. 13 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The dichlorides of commercial 1,4-phenylenediacrylic acid3,3′-(1,4-Phenylene)di-2-propenoic acid. and N-(4-carboxyphenyl)-trimellitimide were polycondensed with a chiral spacer prepared from (S)-3-bromo-2-methylpropanol and 4-mercaptophenol. Optical microscopy revealed that all the resulting copoly(ester-imide)s form an enantiotropic cholesteric melt and adopt a Grandjean texture upon slight shearing. The WAXD powder patterns indicate the formation of a layered structure in the solid state. Irradiation with UV light of wavelength ≤ 360 nm allows crosslinking at any temperature above 25°C. Wiley InterScience Backfile Collection 1832-2000 Kricheldorf, Hans R. oth Probst, Nicolas oth in Macromolecular Chemistry and Physics Weinheim : Wiley-VCH 196(1995) vom: Nov., Seite 3511-3523 (DE-627)NLEJ159071399 (DE-600)1475026-0 1022-1352 nnns volume:196 year:1995 month:11 pages:3511-3523 extent:13 http://dx.doi.org/10.1002/macp.1995.021961106 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 196 1995 11 3511-3523 13 |
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Liquid-crystalline polyimides, 23Part 22: H. R. Kricheldorf, M. Gurau, J. Macromol. Sci., Pure Appl. Chem., in press. Photoreactive, cholesteric copoly(ester-imide)s derived from 1,4-phenylenediacrylic acid and 4-aminobenzoic trimellitimide |
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Liquid-crystalline polyimides, 23Part 22: H. R. Kricheldorf, M. Gurau, J. Macromol. Sci., Pure Appl. Chem., in press. Photoreactive, cholesteric copoly(ester-imide)s derived from 1,4-phenylenediacrylic acid and 4-aminobenzoic trimellitimide |
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The dichlorides of commercial 1,4-phenylenediacrylic acid3,3′-(1,4-Phenylene)di-2-propenoic acid. and N-(4-carboxyphenyl)-trimellitimide were polycondensed with a chiral spacer prepared from (S)-3-bromo-2-methylpropanol and 4-mercaptophenol. Optical microscopy revealed that all the resulting copoly(ester-imide)s form an enantiotropic cholesteric melt and adopt a Grandjean texture upon slight shearing. The WAXD powder patterns indicate the formation of a layered structure in the solid state. Irradiation with UV light of wavelength ≤ 360 nm allows crosslinking at any temperature above 25°C. |
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The dichlorides of commercial 1,4-phenylenediacrylic acid3,3′-(1,4-Phenylene)di-2-propenoic acid. and N-(4-carboxyphenyl)-trimellitimide were polycondensed with a chiral spacer prepared from (S)-3-bromo-2-methylpropanol and 4-mercaptophenol. Optical microscopy revealed that all the resulting copoly(ester-imide)s form an enantiotropic cholesteric melt and adopt a Grandjean texture upon slight shearing. The WAXD powder patterns indicate the formation of a layered structure in the solid state. Irradiation with UV light of wavelength ≤ 360 nm allows crosslinking at any temperature above 25°C. |
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The dichlorides of commercial 1,4-phenylenediacrylic acid3,3′-(1,4-Phenylene)di-2-propenoic acid. and N-(4-carboxyphenyl)-trimellitimide were polycondensed with a chiral spacer prepared from (S)-3-bromo-2-methylpropanol and 4-mercaptophenol. Optical microscopy revealed that all the resulting copoly(ester-imide)s form an enantiotropic cholesteric melt and adopt a Grandjean texture upon slight shearing. The WAXD powder patterns indicate the formation of a layered structure in the solid state. Irradiation with UV light of wavelength ≤ 360 nm allows crosslinking at any temperature above 25°C. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ163460159</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230506102511.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070201s1995 xx |||||o 00| ||eng c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ163460159</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Liquid-crystalline polyimides, 23Part 22: H. R. Kricheldorf, M. Gurau, J. Macromol. Sci., Pure Appl. Chem., in press. Photoreactive, cholesteric copoly(ester-imide)s derived from 1,4-phenylenediacrylic acid and 4-aminobenzoic trimellitimide</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1995</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="b">8 Ill.</subfield><subfield code="b">2 Tab.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">13</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">The dichlorides of commercial 1,4-phenylenediacrylic acid3,3′-(1,4-Phenylene)di-2-propenoic acid. and N-(4-carboxyphenyl)-trimellitimide were polycondensed with a chiral spacer prepared from (S)-3-bromo-2-methylpropanol and 4-mercaptophenol. Optical microscopy revealed that all the resulting copoly(ester-imide)s form an enantiotropic cholesteric melt and adopt a Grandjean texture upon slight shearing. The WAXD powder patterns indicate the formation of a layered structure in the solid state. Irradiation with UV light of wavelength ≤ 360 nm allows crosslinking at any temperature above 25°C.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Wiley InterScience Backfile Collection 1832-2000</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kricheldorf, Hans R.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Probst, Nicolas</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Macromolecular Chemistry and Physics</subfield><subfield code="d">Weinheim : Wiley-VCH</subfield><subfield code="g">196(1995) vom: Nov., Seite 3511-3523</subfield><subfield code="w">(DE-627)NLEJ159071399</subfield><subfield code="w">(DE-600)1475026-0</subfield><subfield code="x">1022-1352</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:196</subfield><subfield code="g">year:1995</subfield><subfield code="g">month:11</subfield><subfield code="g">pages:3511-3523</subfield><subfield code="g">extent:13</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1002/macp.1995.021961106</subfield><subfield code="q">text/html</subfield><subfield code="z">Deutschlandweit zugänglich</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-WIS</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">196</subfield><subfield code="j">1995</subfield><subfield code="c">11</subfield><subfield code="h">3511-3523</subfield><subfield code="g">13</subfield></datafield></record></collection>
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