New thermotropic polyesters from distyrylbenzene bisphenols

Mates, T. E. ; Ober, C. K.

New York : Wiley-Blackwell
Published 1990
ISSN:
0887-6258
Keywords:
Chemistry ; Polymer and Materials Science
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
New main-chain thermotropic liquid crystalline (lc) polymers based on four derivatives of 4,4′- (p-phenylenedi-1,2-ethenediyl)bisphenol have heen prepared by Schotten-Baumen polymerization. Fusibility and solubility were achieved through the incorporation of side groups and flexible methylene spacers. Both a model ester and polymers based on the unsubstituted bisphenol were thermotropic, but had melting points in the vicinity of decomposition. Methyl, methoxy, and ethoxy side groups were used to lower the melting transition. The liquid-crystallinity was investigated with polarized light microscopy, differential scanning calorimetry, and X-ray diffraction. Methyl substitution provided the model compound and polymers with the greatest number of mesophases. Chemical structure was analyzed by infrared and UV/visible spectroscopy, 1H NMR, and elemental analysis of monomers and model compounds. Intrinsic viscosities were measured in N-methylpyrrolidone (nmp) solution.
Additional Material:
4 Ill.
Type of Medium:
Electronic Resource
URL:
_version_ 1798297735553613825
addmaterial 4 Ill.
autor Mates, T. E.
Ober, C. K.
autorsonst Mates, T. E.
Ober, C. K.
book_url http://dx.doi.org/10.1002/pol.1990.140281103
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM163943192
iqvoc_descriptor_keyword iqvoc_00000092:Materials
issn 0887-6258
journal_name Journal of Polymer Science: Polymer Letters Edition
materialart 1
notes New main-chain thermotropic liquid crystalline (lc) polymers based on four derivatives of 4,4′- (p-phenylenedi-1,2-ethenediyl)bisphenol have heen prepared by Schotten-Baumen polymerization. Fusibility and solubility were achieved through the incorporation of side groups and flexible methylene spacers. Both a model ester and polymers based on the unsubstituted bisphenol were thermotropic, but had melting points in the vicinity of decomposition. Methyl, methoxy, and ethoxy side groups were used to lower the melting transition. The liquid-crystallinity was investigated with polarized light microscopy, differential scanning calorimetry, and X-ray diffraction. Methyl substitution provided the model compound and polymers with the greatest number of mesophases. Chemical structure was analyzed by infrared and UV/visible spectroscopy, 1H NMR, and elemental analysis of monomers and model compounds. Intrinsic viscosities were measured in N-methylpyrrolidone (nmp) solution.
package_name Wiley-Blackwell
publikationsjahr_anzeige 1990
publikationsjahr_facette 1990
publikationsjahr_intervall 8009:1990-1994
publikationsjahr_sort 1990
publikationsort New York
publisher Wiley-Blackwell
reference 28 (1990), S. 331-339
schlagwort Chemistry
Polymer and Materials Science
search_space articles
shingle_author_1 Mates, T. E.
Ober, C. K.
shingle_author_2 Mates, T. E.
Ober, C. K.
shingle_author_3 Mates, T. E.
Ober, C. K.
shingle_author_4 Mates, T. E.
Ober, C. K.
shingle_catch_all_1 Mates, T. E.
Ober, C. K.
New thermotropic polyesters from distyrylbenzene bisphenols
Chemistry
Polymer and Materials Science
Chemistry
Polymer and Materials Science
New main-chain thermotropic liquid crystalline (lc) polymers based on four derivatives of 4,4′- (p-phenylenedi-1,2-ethenediyl)bisphenol have heen prepared by Schotten-Baumen polymerization. Fusibility and solubility were achieved through the incorporation of side groups and flexible methylene spacers. Both a model ester and polymers based on the unsubstituted bisphenol were thermotropic, but had melting points in the vicinity of decomposition. Methyl, methoxy, and ethoxy side groups were used to lower the melting transition. The liquid-crystallinity was investigated with polarized light microscopy, differential scanning calorimetry, and X-ray diffraction. Methyl substitution provided the model compound and polymers with the greatest number of mesophases. Chemical structure was analyzed by infrared and UV/visible spectroscopy, 1H NMR, and elemental analysis of monomers and model compounds. Intrinsic viscosities were measured in N-methylpyrrolidone (nmp) solution.
0887-6258
08876258
Wiley-Blackwell
shingle_catch_all_2 Mates, T. E.
Ober, C. K.
New thermotropic polyesters from distyrylbenzene bisphenols
Chemistry
Polymer and Materials Science
Chemistry
Polymer and Materials Science
New main-chain thermotropic liquid crystalline (lc) polymers based on four derivatives of 4,4′- (p-phenylenedi-1,2-ethenediyl)bisphenol have heen prepared by Schotten-Baumen polymerization. Fusibility and solubility were achieved through the incorporation of side groups and flexible methylene spacers. Both a model ester and polymers based on the unsubstituted bisphenol were thermotropic, but had melting points in the vicinity of decomposition. Methyl, methoxy, and ethoxy side groups were used to lower the melting transition. The liquid-crystallinity was investigated with polarized light microscopy, differential scanning calorimetry, and X-ray diffraction. Methyl substitution provided the model compound and polymers with the greatest number of mesophases. Chemical structure was analyzed by infrared and UV/visible spectroscopy, 1H NMR, and elemental analysis of monomers and model compounds. Intrinsic viscosities were measured in N-methylpyrrolidone (nmp) solution.
0887-6258
08876258
Wiley-Blackwell
shingle_catch_all_3 Mates, T. E.
Ober, C. K.
New thermotropic polyesters from distyrylbenzene bisphenols
Chemistry
Polymer and Materials Science
Chemistry
Polymer and Materials Science
New main-chain thermotropic liquid crystalline (lc) polymers based on four derivatives of 4,4′- (p-phenylenedi-1,2-ethenediyl)bisphenol have heen prepared by Schotten-Baumen polymerization. Fusibility and solubility were achieved through the incorporation of side groups and flexible methylene spacers. Both a model ester and polymers based on the unsubstituted bisphenol were thermotropic, but had melting points in the vicinity of decomposition. Methyl, methoxy, and ethoxy side groups were used to lower the melting transition. The liquid-crystallinity was investigated with polarized light microscopy, differential scanning calorimetry, and X-ray diffraction. Methyl substitution provided the model compound and polymers with the greatest number of mesophases. Chemical structure was analyzed by infrared and UV/visible spectroscopy, 1H NMR, and elemental analysis of monomers and model compounds. Intrinsic viscosities were measured in N-methylpyrrolidone (nmp) solution.
0887-6258
08876258
Wiley-Blackwell
shingle_catch_all_4 Mates, T. E.
Ober, C. K.
New thermotropic polyesters from distyrylbenzene bisphenols
Chemistry
Polymer and Materials Science
Chemistry
Polymer and Materials Science
New main-chain thermotropic liquid crystalline (lc) polymers based on four derivatives of 4,4′- (p-phenylenedi-1,2-ethenediyl)bisphenol have heen prepared by Schotten-Baumen polymerization. Fusibility and solubility were achieved through the incorporation of side groups and flexible methylene spacers. Both a model ester and polymers based on the unsubstituted bisphenol were thermotropic, but had melting points in the vicinity of decomposition. Methyl, methoxy, and ethoxy side groups were used to lower the melting transition. The liquid-crystallinity was investigated with polarized light microscopy, differential scanning calorimetry, and X-ray diffraction. Methyl substitution provided the model compound and polymers with the greatest number of mesophases. Chemical structure was analyzed by infrared and UV/visible spectroscopy, 1H NMR, and elemental analysis of monomers and model compounds. Intrinsic viscosities were measured in N-methylpyrrolidone (nmp) solution.
0887-6258
08876258
Wiley-Blackwell
shingle_title_1 New thermotropic polyesters from distyrylbenzene bisphenols
shingle_title_2 New thermotropic polyesters from distyrylbenzene bisphenols
shingle_title_3 New thermotropic polyesters from distyrylbenzene bisphenols
shingle_title_4 New thermotropic polyesters from distyrylbenzene bisphenols
sigel_instance_filter dkfz
geomar
wilbert
ipn
albert
source_archive Wiley InterScience Backfile Collection 1832-2000
timestamp 2024-05-06T10:12:41.645Z
titel New thermotropic polyesters from distyrylbenzene bisphenols
titel_suche New thermotropic polyesters from distyrylbenzene bisphenols
topic V
uid nat_lic_papers_NLM163943192