Fundamental investigations into the free‐radical copolymerization of N ‐phenylmaleimide and norbornene
Abstract
ABSTRACT A fundamental investigation into the copolymerization of N ‐phenylmaleimide and norbornene via conventional free‐radical polymerization techniques was conducted. Reaction conditions were optimized for molecular weight and percent yield by tuning overall concentration and initiator loading. The copolymerization kinetics were monitored using in‐situ , variable temperature nuclear magnetic resonance and first‐order behavior was observed with respect to each monomer. Although the related copolymerization of norbornene and maleic anhydride was well‐known to proceed in a perfectly alternating manner, the copolymerization of norbornene and N ‐phenylmaleimide was found to deviate from strictly alternating copolymerization behavior, producing significant amounts of sequentially enchained N ‐phenylmaleimide units within the polymeric backbone. This deviation from perfectly alternating behavior was confirmed by analysis of individual monomer conversion rates and by measurement of monomer reactivity ratios using the Mayo–Lewis graphical analysis method. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54 , 985–991
- Authors:
-
- Department of Chemistry University of Tennessee Knoxville Tennessee 37996‐1600
- Publication Date:
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 1400526
- Resource Type:
- Publisher's Accepted Manuscript
- Journal Name:
- Journal of Polymer Science. Part A, Polymer Chemistry
- Additional Journal Information:
- Journal Name: Journal of Polymer Science. Part A, Polymer Chemistry Journal Volume: 54 Journal Issue: 7; Journal ID: ISSN 0887-624X
- Publisher:
- Wiley Blackwell (John Wiley & Sons)
- Country of Publication:
- United States
- Language:
- English
Citation Formats
Gmernicki, Kevin R., Cameron, Matthew, and Long, Brian K. Fundamental investigations into the free‐radical copolymerization of N ‐phenylmaleimide and norbornene. United States: N. p., 2015.
Web. doi:10.1002/pola.27934.
Gmernicki, Kevin R., Cameron, Matthew, & Long, Brian K. Fundamental investigations into the free‐radical copolymerization of N ‐phenylmaleimide and norbornene. United States. https://doi.org/10.1002/pola.27934
Gmernicki, Kevin R., Cameron, Matthew, and Long, Brian K. Thu .
"Fundamental investigations into the free‐radical copolymerization of N ‐phenylmaleimide and norbornene". United States. https://doi.org/10.1002/pola.27934.
@article{osti_1400526,
title = {Fundamental investigations into the free‐radical copolymerization of N ‐phenylmaleimide and norbornene},
author = {Gmernicki, Kevin R. and Cameron, Matthew and Long, Brian K.},
abstractNote = {ABSTRACT A fundamental investigation into the copolymerization of N ‐phenylmaleimide and norbornene via conventional free‐radical polymerization techniques was conducted. Reaction conditions were optimized for molecular weight and percent yield by tuning overall concentration and initiator loading. The copolymerization kinetics were monitored using in‐situ , variable temperature nuclear magnetic resonance and first‐order behavior was observed with respect to each monomer. Although the related copolymerization of norbornene and maleic anhydride was well‐known to proceed in a perfectly alternating manner, the copolymerization of norbornene and N ‐phenylmaleimide was found to deviate from strictly alternating copolymerization behavior, producing significant amounts of sequentially enchained N ‐phenylmaleimide units within the polymeric backbone. This deviation from perfectly alternating behavior was confirmed by analysis of individual monomer conversion rates and by measurement of monomer reactivity ratios using the Mayo–Lewis graphical analysis method. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54 , 985–991},
doi = {10.1002/pola.27934},
journal = {Journal of Polymer Science. Part A, Polymer Chemistry},
number = 7,
volume = 54,
place = {United States},
year = {Thu Oct 22 00:00:00 EDT 2015},
month = {Thu Oct 22 00:00:00 EDT 2015}
}
https://doi.org/10.1002/pola.27934
Web of Science
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