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Copolymerization of Phenylselenide-Substituted Maleimide with Styrene and Its Oxidative Elimination Behavior

Selenium-containing monomer monophenyl maleimide selenide (MSM) was synthesized and copolymerized with styrene (St) using reversible addition-fragmentation chain transfer (RAFT) polymerization. Copolymers with controlled molecular weight and narrow molecular weight distribution were obtained. The st...

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Detalles Bibliográficos
Autores principales: Liu, Qian, Lv, Xinghua, Li, Na, Pan, Xiangqiang, Zhu, Jian, Zhu, Xiulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415178/
https://www.ncbi.nlm.nih.gov/pubmed/30966356
http://dx.doi.org/10.3390/polym10030321
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author Liu, Qian
Lv, Xinghua
Li, Na
Pan, Xiangqiang
Zhu, Jian
Zhu, Xiulin
author_facet Liu, Qian
Lv, Xinghua
Li, Na
Pan, Xiangqiang
Zhu, Jian
Zhu, Xiulin
author_sort Liu, Qian
collection PubMed
description Selenium-containing monomer monophenyl maleimide selenide (MSM) was synthesized and copolymerized with styrene (St) using reversible addition-fragmentation chain transfer (RAFT) polymerization. Copolymers with controlled molecular weight and narrow molecular weight distribution were obtained. The structure of the copolymer was characterized by nuclear magnetic resonance, matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrum, Fourier transform infrared spectroscopy (FT-IR) and Ultraviolet–visible spectroscopy (UV-vis) spectroscopy. The copolymer can be oxidized by H(2)O(2) to form carbon-carbon double bonds within the main chain due to the unique sensitivity of selenide groups in the presence of oxidants. Such structure changing resulted in an interesting concentration-related photoluminescence emission enhancement.
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spelling pubmed-64151782019-04-02 Copolymerization of Phenylselenide-Substituted Maleimide with Styrene and Its Oxidative Elimination Behavior Liu, Qian Lv, Xinghua Li, Na Pan, Xiangqiang Zhu, Jian Zhu, Xiulin Polymers (Basel) Article Selenium-containing monomer monophenyl maleimide selenide (MSM) was synthesized and copolymerized with styrene (St) using reversible addition-fragmentation chain transfer (RAFT) polymerization. Copolymers with controlled molecular weight and narrow molecular weight distribution were obtained. The structure of the copolymer was characterized by nuclear magnetic resonance, matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrum, Fourier transform infrared spectroscopy (FT-IR) and Ultraviolet–visible spectroscopy (UV-vis) spectroscopy. The copolymer can be oxidized by H(2)O(2) to form carbon-carbon double bonds within the main chain due to the unique sensitivity of selenide groups in the presence of oxidants. Such structure changing resulted in an interesting concentration-related photoluminescence emission enhancement. MDPI 2018-03-15 /pmc/articles/PMC6415178/ /pubmed/30966356 http://dx.doi.org/10.3390/polym10030321 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Qian
Lv, Xinghua
Li, Na
Pan, Xiangqiang
Zhu, Jian
Zhu, Xiulin
Copolymerization of Phenylselenide-Substituted Maleimide with Styrene and Its Oxidative Elimination Behavior
title Copolymerization of Phenylselenide-Substituted Maleimide with Styrene and Its Oxidative Elimination Behavior
title_full Copolymerization of Phenylselenide-Substituted Maleimide with Styrene and Its Oxidative Elimination Behavior
title_fullStr Copolymerization of Phenylselenide-Substituted Maleimide with Styrene and Its Oxidative Elimination Behavior
title_full_unstemmed Copolymerization of Phenylselenide-Substituted Maleimide with Styrene and Its Oxidative Elimination Behavior
title_short Copolymerization of Phenylselenide-Substituted Maleimide with Styrene and Its Oxidative Elimination Behavior
title_sort copolymerization of phenylselenide-substituted maleimide with styrene and its oxidative elimination behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415178/
https://www.ncbi.nlm.nih.gov/pubmed/30966356
http://dx.doi.org/10.3390/polym10030321
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