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Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids

The synthesis and catalytic reactivity of a class of water-tolerant cationic phosphorus-based Lewis acids is reported. Corrole-based phosphorus(v) cations of the type [ArP(cor)][B(C(6)F(5))(4)] (Ar = C(6)H(5), 3,5-(CF(3))(2)C(6)H(3); cor = 5,10,15-(C(6)H(5))(3)corrolato(3–), 5,10,15-(C(6)F(5))(3)cor...

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Autores principales: Gilhula, James C., Radosevich, Alexander T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685354/
https://www.ncbi.nlm.nih.gov/pubmed/31588285
http://dx.doi.org/10.1039/c9sc02463h
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author Gilhula, James C.
Radosevich, Alexander T.
author_facet Gilhula, James C.
Radosevich, Alexander T.
author_sort Gilhula, James C.
collection PubMed
description The synthesis and catalytic reactivity of a class of water-tolerant cationic phosphorus-based Lewis acids is reported. Corrole-based phosphorus(v) cations of the type [ArP(cor)][B(C(6)F(5))(4)] (Ar = C(6)H(5), 3,5-(CF(3))(2)C(6)H(3); cor = 5,10,15-(C(6)H(5))(3)corrolato(3–), 5,10,15-(C(6)F(5))(3)corrolato(3–)) were synthesized and characterized by NMR and X-ray diffraction. The visible electronic absorption spectra of these cationic phosphacorroles depend strongly on the coordination environment at phosphorus, and their Lewis acidities are quantified by spectrophotometric titrations. DFT analyses establish that the character of the P-acceptor orbital comprises P–N antibonding interactions in the basal plane of the phosphacorrole. Consequently, the cationic phosphacorroles display unprecedented stability to water and alcohols while remaining highly active and robust Lewis acid catalysts for carbonyl hydrosilylation, C(sp(3))–H bond functionalization, and carbohydrate deoxygenation reactions.
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spelling pubmed-66853542019-10-04 Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids Gilhula, James C. Radosevich, Alexander T. Chem Sci Chemistry The synthesis and catalytic reactivity of a class of water-tolerant cationic phosphorus-based Lewis acids is reported. Corrole-based phosphorus(v) cations of the type [ArP(cor)][B(C(6)F(5))(4)] (Ar = C(6)H(5), 3,5-(CF(3))(2)C(6)H(3); cor = 5,10,15-(C(6)H(5))(3)corrolato(3–), 5,10,15-(C(6)F(5))(3)corrolato(3–)) were synthesized and characterized by NMR and X-ray diffraction. The visible electronic absorption spectra of these cationic phosphacorroles depend strongly on the coordination environment at phosphorus, and their Lewis acidities are quantified by spectrophotometric titrations. DFT analyses establish that the character of the P-acceptor orbital comprises P–N antibonding interactions in the basal plane of the phosphacorrole. Consequently, the cationic phosphacorroles display unprecedented stability to water and alcohols while remaining highly active and robust Lewis acid catalysts for carbonyl hydrosilylation, C(sp(3))–H bond functionalization, and carbohydrate deoxygenation reactions. Royal Society of Chemistry 2019-06-18 /pmc/articles/PMC6685354/ /pubmed/31588285 http://dx.doi.org/10.1039/c9sc02463h Text en This journal is © The Royal Society of Chemistry 2019 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Gilhula, James C.
Radosevich, Alexander T.
Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids
title Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids
title_full Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids
title_fullStr Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids
title_full_unstemmed Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids
title_short Tetragonal phosphorus(v) cations as tunable and robust catalytic Lewis acids
title_sort tetragonal phosphorus(v) cations as tunable and robust catalytic lewis acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685354/
https://www.ncbi.nlm.nih.gov/pubmed/31588285
http://dx.doi.org/10.1039/c9sc02463h
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