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Temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates
We report the alternating copolymerization of caprolactone and epoxide through the in situ formation of pre-sequenced spiroorthoester monomer. The reaction is catalyzed by the temperature triggered, bifunctional cationic indium complex (±)-[(NN(i)O(tBu))In(CH(2)SiMe(3))][B(C(6)F(5))(4)] (1). 1 can c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966630/ https://www.ncbi.nlm.nih.gov/pubmed/35432898 http://dx.doi.org/10.1039/d1sc06634j |
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author | Jung, Hyuk-Joon Goonesinghe, Chatura Mehrkhodavandi, Parisa |
author_facet | Jung, Hyuk-Joon Goonesinghe, Chatura Mehrkhodavandi, Parisa |
author_sort | Jung, Hyuk-Joon |
collection | PubMed |
description | We report the alternating copolymerization of caprolactone and epoxide through the in situ formation of pre-sequenced spiroorthoester monomer. The reaction is catalyzed by the temperature triggered, bifunctional cationic indium complex (±)-[(NN(i)O(tBu))In(CH(2)SiMe(3))][B(C(6)F(5))(4)] (1). 1 can catalyze the coupling of epoxide and lactone to form spiroorthoester at 60 °C and its double ring-opening polymerization at 110 °C to form poly(ether-alt-ester). The post-polymerization modification and degradation of the poly(ether-alt-ester) are further investigated. |
format | Online Article Text |
id | pubmed-8966630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-89666302022-04-14 Temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates Jung, Hyuk-Joon Goonesinghe, Chatura Mehrkhodavandi, Parisa Chem Sci Chemistry We report the alternating copolymerization of caprolactone and epoxide through the in situ formation of pre-sequenced spiroorthoester monomer. The reaction is catalyzed by the temperature triggered, bifunctional cationic indium complex (±)-[(NN(i)O(tBu))In(CH(2)SiMe(3))][B(C(6)F(5))(4)] (1). 1 can catalyze the coupling of epoxide and lactone to form spiroorthoester at 60 °C and its double ring-opening polymerization at 110 °C to form poly(ether-alt-ester). The post-polymerization modification and degradation of the poly(ether-alt-ester) are further investigated. The Royal Society of Chemistry 2022-03-16 /pmc/articles/PMC8966630/ /pubmed/35432898 http://dx.doi.org/10.1039/d1sc06634j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Jung, Hyuk-Joon Goonesinghe, Chatura Mehrkhodavandi, Parisa Temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates |
title | Temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates |
title_full | Temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates |
title_fullStr | Temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates |
title_full_unstemmed | Temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates |
title_short | Temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates |
title_sort | temperature triggered alternating copolymerization of epoxides and lactones via pre-sequenced spiroorthoester intermediates |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966630/ https://www.ncbi.nlm.nih.gov/pubmed/35432898 http://dx.doi.org/10.1039/d1sc06634j |
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