Dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane

In the crystal structure of the title compound, C(39)H(54)BCl(2)P, the phospho­rus atom is coordinated by a dichloro­phenyl­borane unit. The substituted biphenyl group and the two cyclo­hexyl groups at the phospho­rus atom are arranged in such a way to avoid steric crowding in the mol­ecule as far a...

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Detalles Bibliográficos
Autores principales: Braunschweig, Holger, Dewhurst, Rian D., Radacki, Krzysztof, Wagner, Katharina
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971049/
https://www.ncbi.nlm.nih.gov/pubmed/21578380
http://dx.doi.org/10.1107/S1600536809041865
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author Braunschweig, Holger
Dewhurst, Rian D.
Radacki, Krzysztof
Wagner, Katharina
author_facet Braunschweig, Holger
Dewhurst, Rian D.
Radacki, Krzysztof
Wagner, Katharina
author_sort Braunschweig, Holger
collection PubMed
description In the crystal structure of the title compound, C(39)H(54)BCl(2)P, the phospho­rus atom is coordinated by a dichloro­phenyl­borane unit. The substituted biphenyl group and the two cyclo­hexyl groups at the phospho­rus atom are arranged in such a way to avoid steric crowding in the mol­ecule as far as possible.
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spelling pubmed-29710492010-12-30 Dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane Braunschweig, Holger Dewhurst, Rian D. Radacki, Krzysztof Wagner, Katharina Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(39)H(54)BCl(2)P, the phospho­rus atom is coordinated by a dichloro­phenyl­borane unit. The substituted biphenyl group and the two cyclo­hexyl groups at the phospho­rus atom are arranged in such a way to avoid steric crowding in the mol­ecule as far as possible. International Union of Crystallography 2009-10-17 /pmc/articles/PMC2971049/ /pubmed/21578380 http://dx.doi.org/10.1107/S1600536809041865 Text en © Braunschweig et al. 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Braunschweig, Holger
Dewhurst, Rian D.
Radacki, Krzysztof
Wagner, Katharina
Dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane
title Dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane
title_full Dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane
title_fullStr Dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane
title_full_unstemmed Dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane
title_short Dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane
title_sort dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine–dichlorophenylborane
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971049/
https://www.ncbi.nlm.nih.gov/pubmed/21578380
http://dx.doi.org/10.1107/S1600536809041865
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