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Reductive Elimination from Sterically Encumbered Ni–Polypyridine Complexes
[Image: see text] Herein we disclose the synthesis of sterically encumbered dialkylnickel(II) complexes bearing 2,9-dimethyl-1,10-phenanthroline ligands. A comparison with their unsubstituted analogues by both X-ray crystallography and theoretical calculations revealed significant distortions in the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554914/ https://www.ncbi.nlm.nih.gov/pubmed/36249447 http://dx.doi.org/10.1021/acs.organomet.2c00362 |
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author | Day, Craig S. Ton, Stephanie J. McGuire, Ryan T. Foroutan-Nejad, Cina Martin, Ruben |
author_facet | Day, Craig S. Ton, Stephanie J. McGuire, Ryan T. Foroutan-Nejad, Cina Martin, Ruben |
author_sort | Day, Craig S. |
collection | PubMed |
description | [Image: see text] Herein we disclose the synthesis of sterically encumbered dialkylnickel(II) complexes bearing 2,9-dimethyl-1,10-phenanthroline ligands. A comparison with their unsubstituted analogues by both X-ray crystallography and theoretical calculations revealed significant distortions in their molecular structures. Eyring plots along with stoichiometric and photoexcitation studies revealed that sterically encumbered dialkylnickel(II) complexes enable facile C(sp(3))–C(sp(3)) reductive elimination, thus offering an improved understanding of Ni catalysis. |
format | Online Article Text |
id | pubmed-9554914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95549142022-10-13 Reductive Elimination from Sterically Encumbered Ni–Polypyridine Complexes Day, Craig S. Ton, Stephanie J. McGuire, Ryan T. Foroutan-Nejad, Cina Martin, Ruben Organometallics [Image: see text] Herein we disclose the synthesis of sterically encumbered dialkylnickel(II) complexes bearing 2,9-dimethyl-1,10-phenanthroline ligands. A comparison with their unsubstituted analogues by both X-ray crystallography and theoretical calculations revealed significant distortions in their molecular structures. Eyring plots along with stoichiometric and photoexcitation studies revealed that sterically encumbered dialkylnickel(II) complexes enable facile C(sp(3))–C(sp(3)) reductive elimination, thus offering an improved understanding of Ni catalysis. American Chemical Society 2022-09-21 2022-10-10 /pmc/articles/PMC9554914/ /pubmed/36249447 http://dx.doi.org/10.1021/acs.organomet.2c00362 Text en © 2022 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 | Day, Craig S. Ton, Stephanie J. McGuire, Ryan T. Foroutan-Nejad, Cina Martin, Ruben Reductive Elimination from Sterically Encumbered Ni–Polypyridine Complexes |
title | Reductive
Elimination from Sterically Encumbered Ni–Polypyridine
Complexes |
title_full | Reductive
Elimination from Sterically Encumbered Ni–Polypyridine
Complexes |
title_fullStr | Reductive
Elimination from Sterically Encumbered Ni–Polypyridine
Complexes |
title_full_unstemmed | Reductive
Elimination from Sterically Encumbered Ni–Polypyridine
Complexes |
title_short | Reductive
Elimination from Sterically Encumbered Ni–Polypyridine
Complexes |
title_sort | reductive
elimination from sterically encumbered ni–polypyridine
complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554914/ https://www.ncbi.nlm.nih.gov/pubmed/36249447 http://dx.doi.org/10.1021/acs.organomet.2c00362 |
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