Synthesis of new terpolymers with heterocyclic pendant groups

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(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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Detalles Bibliográficos
Autores principales: Vega, I.N., Sánchez, L., D'Accorso, N.B.
Formato: JOUR
Materias:
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
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_0022152X_v44_n2_p389_Vega
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id todo:paper_0022152X_v44_n2_p389_Vega
record_format dspace
spelling todo:paper_0022152X_v44_n2_p389_Vega2023-10-03T14:27:49Z Synthesis of new terpolymers with heterocyclic pendant groups Vega, I.N. Sánchez, L. D'Accorso, N.B. 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar 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
Vega, I.N.
Sánchez, L.
D'Accorso, N.B.
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.
format JOUR
author Vega, I.N.
Sánchez, L.
D'Accorso, N.B.
author_facet Vega, I.N.
Sánchez, L.
D'Accorso, N.B.
author_sort Vega, I.N.
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
url http://hdl.handle.net/20.500.12110/paper_0022152X_v44_n2_p389_Vega
work_keys_str_mv AT vegain synthesisofnewterpolymerswithheterocyclicpendantgroups
AT sanchezl synthesisofnewterpolymerswithheterocyclicpendantgroups
AT daccorsonb synthesisofnewterpolymerswithheterocyclicpendantgroups
_version_ 1807314405512183808

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