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Nickel Complexes of Allyl and Vinyldiphenylphosphine

[Image: see text] Monodentate phosphine-ligated nickel compounds, e.g., [Ni(PPh(3))(4)] are relevant as active catalysts across a broad range of reactions. This report expands upon the coordination chemistry of this family, offering the reactivity of allyl- and vinyl-substituted diphenylphosphine (P...

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Autores principales: Clapson, Marissa L., Nelson, David J., Drover, Marcus W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401672/
https://www.ncbi.nlm.nih.gov/pubmed/37545661
http://dx.doi.org/10.1021/acsorginorgau.3c00010
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author Clapson, Marissa L.
Nelson, David J.
Drover, Marcus W.
author_facet Clapson, Marissa L.
Nelson, David J.
Drover, Marcus W.
author_sort Clapson, Marissa L.
collection PubMed
description [Image: see text] Monodentate phosphine-ligated nickel compounds, e.g., [Ni(PPh(3))(4)] are relevant as active catalysts across a broad range of reactions. This report expands upon the coordination chemistry of this family, offering the reactivity of allyl- and vinyl-substituted diphenylphosphine (PPh(2)R) with [Ni(COD)(2)] (COD = 1,5-cyclooctadiene). These reactions provide three-coordinate dinickelacycles that are intermolecularly tethered through adjacent {Ni}-olefin interactions. The ring conformation of such cycles has been studied in the solid-state and using theoretical calculations. Here, a difference in reaction outcome is linked to the presence of an allyl vs vinyl group, where the former is observed to undergo rearrangement, bringing about challenges in clean product isolation.
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spelling pubmed-104016722023-08-05 Nickel Complexes of Allyl and Vinyldiphenylphosphine Clapson, Marissa L. Nelson, David J. Drover, Marcus W. ACS Org Inorg Au [Image: see text] Monodentate phosphine-ligated nickel compounds, e.g., [Ni(PPh(3))(4)] are relevant as active catalysts across a broad range of reactions. This report expands upon the coordination chemistry of this family, offering the reactivity of allyl- and vinyl-substituted diphenylphosphine (PPh(2)R) with [Ni(COD)(2)] (COD = 1,5-cyclooctadiene). These reactions provide three-coordinate dinickelacycles that are intermolecularly tethered through adjacent {Ni}-olefin interactions. The ring conformation of such cycles has been studied in the solid-state and using theoretical calculations. Here, a difference in reaction outcome is linked to the presence of an allyl vs vinyl group, where the former is observed to undergo rearrangement, bringing about challenges in clean product isolation. American Chemical Society 2023-05-11 /pmc/articles/PMC10401672/ /pubmed/37545661 http://dx.doi.org/10.1021/acsorginorgau.3c00010 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clapson, Marissa L.
Nelson, David J.
Drover, Marcus W.
Nickel Complexes of Allyl and Vinyldiphenylphosphine
title Nickel Complexes of Allyl and Vinyldiphenylphosphine
title_full Nickel Complexes of Allyl and Vinyldiphenylphosphine
title_fullStr Nickel Complexes of Allyl and Vinyldiphenylphosphine
title_full_unstemmed Nickel Complexes of Allyl and Vinyldiphenylphosphine
title_short Nickel Complexes of Allyl and Vinyldiphenylphosphine
title_sort nickel complexes of allyl and vinyldiphenylphosphine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401672/
https://www.ncbi.nlm.nih.gov/pubmed/37545661
http://dx.doi.org/10.1021/acsorginorgau.3c00010
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