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Synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates
Naturally occurring phyllosilicate minerals such as talc and vermiculite in conjunction with n-tetra butyl ammonium bromide (TBAB) co-catalyst were found to be efficient in the coupling of CO(2) with epoxides to form cyclic carbonates. The reaction was carried out in a pressurized autoclave reactor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576757/ https://www.ncbi.nlm.nih.gov/pubmed/33094290 http://dx.doi.org/10.1186/s13065-020-00713-2 |
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author | Nakibuule, Fiona Nyanzi, Steven Allan Oshchapovsky, Igor Wendt, Ola F. Tebandeke, Emmanuel |
author_facet | Nakibuule, Fiona Nyanzi, Steven Allan Oshchapovsky, Igor Wendt, Ola F. Tebandeke, Emmanuel |
author_sort | Nakibuule, Fiona |
collection | PubMed |
description | Naturally occurring phyllosilicate minerals such as talc and vermiculite in conjunction with n-tetra butyl ammonium bromide (TBAB) co-catalyst were found to be efficient in the coupling of CO(2) with epoxides to form cyclic carbonates. The reaction was carried out in a pressurized autoclave reactor at moderate pressures of 10–35 bars and temperatures of 100–150 °C. The optimized catalyst system exhibited > 90% conversion of the epoxides and > 90% selectivity for the desired cyclic carbonates, in the presence or absence of a solvent. The selectivity of the catalytic system could be improved with heat pre-treatment of the phyllosilicates albeit this resulted in slightly lower epoxide conversion. The results obtained using the heat treated phyllosilicates strongly support the hydrogen bond assisted mechanism for the cycloaddition of epoxides and CO(2). The cycloaddition reaction could also be carried out in the absence of TBAB, although lower cyclic carbonate yields were observed. The phyllosilicate part of the catalyst system is heterogeneous, easy to separate after completion of reactions and reusable a number of runs without loss of activity. |
format | Online Article Text |
id | pubmed-7576757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-75767572020-10-21 Synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates Nakibuule, Fiona Nyanzi, Steven Allan Oshchapovsky, Igor Wendt, Ola F. Tebandeke, Emmanuel BMC Chem Research Article Naturally occurring phyllosilicate minerals such as talc and vermiculite in conjunction with n-tetra butyl ammonium bromide (TBAB) co-catalyst were found to be efficient in the coupling of CO(2) with epoxides to form cyclic carbonates. The reaction was carried out in a pressurized autoclave reactor at moderate pressures of 10–35 bars and temperatures of 100–150 °C. The optimized catalyst system exhibited > 90% conversion of the epoxides and > 90% selectivity for the desired cyclic carbonates, in the presence or absence of a solvent. The selectivity of the catalytic system could be improved with heat pre-treatment of the phyllosilicates albeit this resulted in slightly lower epoxide conversion. The results obtained using the heat treated phyllosilicates strongly support the hydrogen bond assisted mechanism for the cycloaddition of epoxides and CO(2). The cycloaddition reaction could also be carried out in the absence of TBAB, although lower cyclic carbonate yields were observed. The phyllosilicate part of the catalyst system is heterogeneous, easy to separate after completion of reactions and reusable a number of runs without loss of activity. Springer International Publishing 2020-10-20 /pmc/articles/PMC7576757/ /pubmed/33094290 http://dx.doi.org/10.1186/s13065-020-00713-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Nakibuule, Fiona Nyanzi, Steven Allan Oshchapovsky, Igor Wendt, Ola F. Tebandeke, Emmanuel Synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates |
title | Synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates |
title_full | Synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates |
title_fullStr | Synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates |
title_full_unstemmed | Synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates |
title_short | Synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates |
title_sort | synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by talc and other phyllosilicates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576757/ https://www.ncbi.nlm.nih.gov/pubmed/33094290 http://dx.doi.org/10.1186/s13065-020-00713-2 |
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