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Application of Green Solvents: PEG and scCO(2) in the Mono- or Biphasic Catalytic Systems for the Repetitive Batch Coupling of Vinylsilanes with Vinyl Boronates toward 1-Boryl-1-silylethenes
[Image: see text] A new method for the repetitive batch silylative coupling (trans-silylation) of vinylsilanes with vinyl boronates in the presence of Ru(CO)Cl(H)(PCy(3))(2) immobilized in poly(ethylene glycols) (PEGs) has been developed. Three PEGs (PEG600, PEG2000, and MPEG2000) with different mol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735702/ https://www.ncbi.nlm.nih.gov/pubmed/33232139 http://dx.doi.org/10.1021/acs.inorgchem.0c02796 |
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author | Ludwiczak, Monika Szyling, Jakub Garbicz, Adriana Sokolnicki, Tomasz Pyziak, Jadwiga Walkowiak, Jȩdrzej |
author_facet | Ludwiczak, Monika Szyling, Jakub Garbicz, Adriana Sokolnicki, Tomasz Pyziak, Jadwiga Walkowiak, Jȩdrzej |
author_sort | Ludwiczak, Monika |
collection | PubMed |
description | [Image: see text] A new method for the repetitive batch silylative coupling (trans-silylation) of vinylsilanes with vinyl boronates in the presence of Ru(CO)Cl(H)(PCy(3))(2) immobilized in poly(ethylene glycols) (PEGs) has been developed. Three PEGs (PEG600, PEG2000, and MPEG2000) with different molecular weights and end groups (MW = 600–2000) were tested as solvents and immobilization media, while an aliphatic solvent (n-hexane or n-heptane) or supercritical CO(2) was used for product extraction. By applying 2 mol % of the Ru–H catalyst, it was possible to carry out up to 15 complete runs, with the predominant formation of 1-boryl-1-silylethenes. This immobilization strategy permitted for catalyst reuse and obtaining higher TON values (approximately 660–734) compared to the reaction in conventional solvents (∼50). Detailed kinetic studies of the most effective catalytic system were performed to determine catalyst activity and stability. Moreover, the reactions were carried out in an MPEG2000/scCO(2) biphasic system, positively influencing the process sustainability. |
format | Online Article Text |
id | pubmed-7735702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77357022020-12-15 Application of Green Solvents: PEG and scCO(2) in the Mono- or Biphasic Catalytic Systems for the Repetitive Batch Coupling of Vinylsilanes with Vinyl Boronates toward 1-Boryl-1-silylethenes Ludwiczak, Monika Szyling, Jakub Garbicz, Adriana Sokolnicki, Tomasz Pyziak, Jadwiga Walkowiak, Jȩdrzej Inorg Chem [Image: see text] A new method for the repetitive batch silylative coupling (trans-silylation) of vinylsilanes with vinyl boronates in the presence of Ru(CO)Cl(H)(PCy(3))(2) immobilized in poly(ethylene glycols) (PEGs) has been developed. Three PEGs (PEG600, PEG2000, and MPEG2000) with different molecular weights and end groups (MW = 600–2000) were tested as solvents and immobilization media, while an aliphatic solvent (n-hexane or n-heptane) or supercritical CO(2) was used for product extraction. By applying 2 mol % of the Ru–H catalyst, it was possible to carry out up to 15 complete runs, with the predominant formation of 1-boryl-1-silylethenes. This immobilization strategy permitted for catalyst reuse and obtaining higher TON values (approximately 660–734) compared to the reaction in conventional solvents (∼50). Detailed kinetic studies of the most effective catalytic system were performed to determine catalyst activity and stability. Moreover, the reactions were carried out in an MPEG2000/scCO(2) biphasic system, positively influencing the process sustainability. American Chemical Society 2020-11-24 2020-12-07 /pmc/articles/PMC7735702/ /pubmed/33232139 http://dx.doi.org/10.1021/acs.inorgchem.0c02796 Text en © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Ludwiczak, Monika Szyling, Jakub Garbicz, Adriana Sokolnicki, Tomasz Pyziak, Jadwiga Walkowiak, Jȩdrzej Application of Green Solvents: PEG and scCO(2) in the Mono- or Biphasic Catalytic Systems for the Repetitive Batch Coupling of Vinylsilanes with Vinyl Boronates toward 1-Boryl-1-silylethenes |
title | Application of Green Solvents: PEG and scCO(2) in the Mono-
or Biphasic Catalytic Systems for the Repetitive Batch
Coupling of Vinylsilanes with Vinyl Boronates toward 1-Boryl-1-silylethenes |
title_full | Application of Green Solvents: PEG and scCO(2) in the Mono-
or Biphasic Catalytic Systems for the Repetitive Batch
Coupling of Vinylsilanes with Vinyl Boronates toward 1-Boryl-1-silylethenes |
title_fullStr | Application of Green Solvents: PEG and scCO(2) in the Mono-
or Biphasic Catalytic Systems for the Repetitive Batch
Coupling of Vinylsilanes with Vinyl Boronates toward 1-Boryl-1-silylethenes |
title_full_unstemmed | Application of Green Solvents: PEG and scCO(2) in the Mono-
or Biphasic Catalytic Systems for the Repetitive Batch
Coupling of Vinylsilanes with Vinyl Boronates toward 1-Boryl-1-silylethenes |
title_short | Application of Green Solvents: PEG and scCO(2) in the Mono-
or Biphasic Catalytic Systems for the Repetitive Batch
Coupling of Vinylsilanes with Vinyl Boronates toward 1-Boryl-1-silylethenes |
title_sort | application of green solvents: peg and scco(2) in the mono-
or biphasic catalytic systems for the repetitive batch
coupling of vinylsilanes with vinyl boronates toward 1-boryl-1-silylethenes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735702/ https://www.ncbi.nlm.nih.gov/pubmed/33232139 http://dx.doi.org/10.1021/acs.inorgchem.0c02796 |
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