Synthesis of new terpolymers with heterocyclic pendant groups
(Chemical Equation Presented) Chemical modifications of polyacrylonitrile (PAN), an inexpensive and commercial homopolymer, to obtain terpolymers containing 1,2,4 or 1,3,4 oxadiazolic pendant groups are described. These new materials are physically and spectroscopic ally characterized.
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2007
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v44_n2_p389_Vega http://hdl.handle.net/20.500.12110/paper_0022152X_v44_n2_p389_Vega |
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paper:paper_0022152X_v44_n2_p389_Vega2023-06-08T14:46:50Z Synthesis of new terpolymers with heterocyclic pendant groups amidoxime nitrile 2 chlorophenyl 1,2,4 oxadiazole terpolymer amidoxime nitrile 3 methyl 1,2,4 oxadiazole terpolymer amidoxime nitrile 4 nitrophenyl 1,2,4 oxadiazole terpolymer amidoxime nitrile phenyl 1,2,4 oxadiazole oxadiazole derivative polyacrylonitrile tetrazole nitrile 2 hydroxyphenyl 1,3,4 oxadiazole tetrazole nitrile n aminophenyl 1,3,4 oxadiazole unclassified drug article chemical structure polymerization synthesis thermostability viscometry (Chemical Equation Presented) Chemical modifications of polyacrylonitrile (PAN), an inexpensive and commercial homopolymer, to obtain terpolymers containing 1,2,4 or 1,3,4 oxadiazolic pendant groups are described. These new materials are physically and spectroscopic ally characterized. 2007 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v44_n2_p389_Vega http://hdl.handle.net/20.500.12110/paper_0022152X_v44_n2_p389_Vega |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
amidoxime nitrile 2 chlorophenyl 1,2,4 oxadiazole terpolymer amidoxime nitrile 3 methyl 1,2,4 oxadiazole terpolymer amidoxime nitrile 4 nitrophenyl 1,2,4 oxadiazole terpolymer amidoxime nitrile phenyl 1,2,4 oxadiazole oxadiazole derivative polyacrylonitrile tetrazole nitrile 2 hydroxyphenyl 1,3,4 oxadiazole tetrazole nitrile n aminophenyl 1,3,4 oxadiazole unclassified drug article chemical structure polymerization synthesis thermostability viscometry |
| spellingShingle |
amidoxime nitrile 2 chlorophenyl 1,2,4 oxadiazole terpolymer amidoxime nitrile 3 methyl 1,2,4 oxadiazole terpolymer amidoxime nitrile 4 nitrophenyl 1,2,4 oxadiazole terpolymer amidoxime nitrile phenyl 1,2,4 oxadiazole oxadiazole derivative polyacrylonitrile tetrazole nitrile 2 hydroxyphenyl 1,3,4 oxadiazole tetrazole nitrile n aminophenyl 1,3,4 oxadiazole unclassified drug article chemical structure polymerization synthesis thermostability viscometry Synthesis of new terpolymers with heterocyclic pendant groups |
| topic_facet |
amidoxime nitrile 2 chlorophenyl 1,2,4 oxadiazole terpolymer amidoxime nitrile 3 methyl 1,2,4 oxadiazole terpolymer amidoxime nitrile 4 nitrophenyl 1,2,4 oxadiazole terpolymer amidoxime nitrile phenyl 1,2,4 oxadiazole oxadiazole derivative polyacrylonitrile tetrazole nitrile 2 hydroxyphenyl 1,3,4 oxadiazole tetrazole nitrile n aminophenyl 1,3,4 oxadiazole unclassified drug article chemical structure polymerization synthesis thermostability viscometry |
| description |
(Chemical Equation Presented) Chemical modifications of polyacrylonitrile (PAN), an inexpensive and commercial homopolymer, to obtain terpolymers containing 1,2,4 or 1,3,4 oxadiazolic pendant groups are described. These new materials are physically and spectroscopic ally characterized. |
| title |
Synthesis of new terpolymers with heterocyclic pendant groups |
| title_short |
Synthesis of new terpolymers with heterocyclic pendant groups |
| title_full |
Synthesis of new terpolymers with heterocyclic pendant groups |
| title_fullStr |
Synthesis of new terpolymers with heterocyclic pendant groups |
| title_full_unstemmed |
Synthesis of new terpolymers with heterocyclic pendant groups |
| title_sort |
synthesis of new terpolymers with heterocyclic pendant groups |
| publishDate |
2007 |
| url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v44_n2_p389_Vega http://hdl.handle.net/20.500.12110/paper_0022152X_v44_n2_p389_Vega |
| _version_ |
1768544118914416640 |