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Copolymerization of CO(2) and epoxides mediated by zinc organyls

Herein we report the copolymerization of CHO with CO(2) in the presence of various zinc compounds R(2)Zn (R = Et, Bu, iPr, Cy and Ph). Several zinc organyls proved to be efficient catalysts for this reaction in the absence of water and co-catalyst. Notably, readily available Bu(2)Zn reached a TON up...

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Autores principales: Wulf, Christoph, Doering, Ulrike, Werner, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077689/
https://www.ncbi.nlm.nih.gov/pubmed/35542906
http://dx.doi.org/10.1039/c7ra12535f
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author Wulf, Christoph
Doering, Ulrike
Werner, Thomas
author_facet Wulf, Christoph
Doering, Ulrike
Werner, Thomas
author_sort Wulf, Christoph
collection PubMed
description Herein we report the copolymerization of CHO with CO(2) in the presence of various zinc compounds R(2)Zn (R = Et, Bu, iPr, Cy and Ph). Several zinc organyls proved to be efficient catalysts for this reaction in the absence of water and co-catalyst. Notably, readily available Bu(2)Zn reached a TON up to 269 and an initial TOF up to 91 h(−1). The effect of various parameters on the reaction outcome has been investigated. Poly(ether)carbonates with molecular weights up to 79.3 kg mol(−1) and a CO(2) content of up to 97% were obtained. Under standard reaction conditions (100 °C, 2.0 MPa, 16 h) the influence of commonly employed co-catalysts such as PPNCl and TBAB has been investigated in the presence of Et(2)Zn (0.5 mol%). The reaction of other epoxides (e.g. propylene and styrene oxide) under these conditions led to no significant conversion or to the formation of the respective cyclic carbonate as the main product.
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spelling pubmed-90776892022-05-09 Copolymerization of CO(2) and epoxides mediated by zinc organyls Wulf, Christoph Doering, Ulrike Werner, Thomas RSC Adv Chemistry Herein we report the copolymerization of CHO with CO(2) in the presence of various zinc compounds R(2)Zn (R = Et, Bu, iPr, Cy and Ph). Several zinc organyls proved to be efficient catalysts for this reaction in the absence of water and co-catalyst. Notably, readily available Bu(2)Zn reached a TON up to 269 and an initial TOF up to 91 h(−1). The effect of various parameters on the reaction outcome has been investigated. Poly(ether)carbonates with molecular weights up to 79.3 kg mol(−1) and a CO(2) content of up to 97% were obtained. Under standard reaction conditions (100 °C, 2.0 MPa, 16 h) the influence of commonly employed co-catalysts such as PPNCl and TBAB has been investigated in the presence of Et(2)Zn (0.5 mol%). The reaction of other epoxides (e.g. propylene and styrene oxide) under these conditions led to no significant conversion or to the formation of the respective cyclic carbonate as the main product. The Royal Society of Chemistry 2018-01-18 /pmc/articles/PMC9077689/ /pubmed/35542906 http://dx.doi.org/10.1039/c7ra12535f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Wulf, Christoph
Doering, Ulrike
Werner, Thomas
Copolymerization of CO(2) and epoxides mediated by zinc organyls
title Copolymerization of CO(2) and epoxides mediated by zinc organyls
title_full Copolymerization of CO(2) and epoxides mediated by zinc organyls
title_fullStr Copolymerization of CO(2) and epoxides mediated by zinc organyls
title_full_unstemmed Copolymerization of CO(2) and epoxides mediated by zinc organyls
title_short Copolymerization of CO(2) and epoxides mediated by zinc organyls
title_sort copolymerization of co(2) and epoxides mediated by zinc organyls
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077689/
https://www.ncbi.nlm.nih.gov/pubmed/35542906
http://dx.doi.org/10.1039/c7ra12535f
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