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Rhenium Complexes Bearing Tridentate and Bidentate Phosphinoamine Ligands in the Production of Biofuel Alcohols via the Guerbet Reaction
[Image: see text] We report a variety of rhenium complexes supported by bidentate and tridentate phosphinoamine ligands and their use in the formation of the advanced biofuel isobutanol from methanol and ethanol. Rhenium pincer complexes 1–3 are effective catalysts for this process, with 2 giving is...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8411595/ https://www.ncbi.nlm.nih.gov/pubmed/34483434 http://dx.doi.org/10.1021/acs.organomet.1c00313 |
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author | King, Ashley M. Wingad, Richard L. Pridmore, Natalie E. Pringle, Paul G. Wass, Duncan F. |
author_facet | King, Ashley M. Wingad, Richard L. Pridmore, Natalie E. Pringle, Paul G. Wass, Duncan F. |
author_sort | King, Ashley M. |
collection | PubMed |
description | [Image: see text] We report a variety of rhenium complexes supported by bidentate and tridentate phosphinoamine ligands and their use in the formation of the advanced biofuel isobutanol from methanol and ethanol. Rhenium pincer complexes 1–3 are effective catalysts for this process, with 2 giving isobutanol in 35% yields, with 97% selectivity in the liquid fraction, over 16 h with catalyst loadings as low as 0.07 mol %. However, these catalysts show poorer overall selectivity, with the formation of a significant amount of carboxylate salt solid byproduct also being observed. Production of the active catalyst 1d has been followed by (31)P NMR spectroscopy, and the importance of the presence of base and elevated temperatures to catalyst activation has been established. Complexes supported by diphosphine ligands are inactive for Guerbet chemistry; however, complexes supported by bidentate phosphinoamine ligands show greater selectivity for isobutanol formation over carboxylate salts. The novel complex 7 was able to produce isobutanol in 28% yield over 17 h. The importance of the N–H moiety to the catalytic performance has also been established, giving further weight to the hypothesis that these catalysts operate via a cooperative mechanism. |
format | Online Article Text |
id | pubmed-8411595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-84115952021-09-03 Rhenium Complexes Bearing Tridentate and Bidentate Phosphinoamine Ligands in the Production of Biofuel Alcohols via the Guerbet Reaction King, Ashley M. Wingad, Richard L. Pridmore, Natalie E. Pringle, Paul G. Wass, Duncan F. Organometallics [Image: see text] We report a variety of rhenium complexes supported by bidentate and tridentate phosphinoamine ligands and their use in the formation of the advanced biofuel isobutanol from methanol and ethanol. Rhenium pincer complexes 1–3 are effective catalysts for this process, with 2 giving isobutanol in 35% yields, with 97% selectivity in the liquid fraction, over 16 h with catalyst loadings as low as 0.07 mol %. However, these catalysts show poorer overall selectivity, with the formation of a significant amount of carboxylate salt solid byproduct also being observed. Production of the active catalyst 1d has been followed by (31)P NMR spectroscopy, and the importance of the presence of base and elevated temperatures to catalyst activation has been established. Complexes supported by diphosphine ligands are inactive for Guerbet chemistry; however, complexes supported by bidentate phosphinoamine ligands show greater selectivity for isobutanol formation over carboxylate salts. The novel complex 7 was able to produce isobutanol in 28% yield over 17 h. The importance of the N–H moiety to the catalytic performance has also been established, giving further weight to the hypothesis that these catalysts operate via a cooperative mechanism. American Chemical Society 2021-08-04 2021-08-23 /pmc/articles/PMC8411595/ /pubmed/34483434 http://dx.doi.org/10.1021/acs.organomet.1c00313 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | King, Ashley M. Wingad, Richard L. Pridmore, Natalie E. Pringle, Paul G. Wass, Duncan F. Rhenium Complexes Bearing Tridentate and Bidentate Phosphinoamine Ligands in the Production of Biofuel Alcohols via the Guerbet Reaction |
title | Rhenium Complexes Bearing Tridentate and Bidentate
Phosphinoamine Ligands in the Production of Biofuel Alcohols via the
Guerbet Reaction |
title_full | Rhenium Complexes Bearing Tridentate and Bidentate
Phosphinoamine Ligands in the Production of Biofuel Alcohols via the
Guerbet Reaction |
title_fullStr | Rhenium Complexes Bearing Tridentate and Bidentate
Phosphinoamine Ligands in the Production of Biofuel Alcohols via the
Guerbet Reaction |
title_full_unstemmed | Rhenium Complexes Bearing Tridentate and Bidentate
Phosphinoamine Ligands in the Production of Biofuel Alcohols via the
Guerbet Reaction |
title_short | Rhenium Complexes Bearing Tridentate and Bidentate
Phosphinoamine Ligands in the Production of Biofuel Alcohols via the
Guerbet Reaction |
title_sort | rhenium complexes bearing tridentate and bidentate
phosphinoamine ligands in the production of biofuel alcohols via the
guerbet reaction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8411595/ https://www.ncbi.nlm.nih.gov/pubmed/34483434 http://dx.doi.org/10.1021/acs.organomet.1c00313 |
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