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Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines

Stepwise oxidation of 1,8-bis(diphenylphosphino)naphthalene and a series of (oligo)methylene-linked diphosphines with XeF(2) followed by fluoride abstraction yields a family of compounds featuring phosphine, phosphonium and phosphorane moieties in close proximity. The bisphosphonium ions [(C(10)H(6)...

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Detalles Bibliográficos
Autores principales: Holthausen, Michael H., Hiranandani, Rashi R., Stephan, Douglas W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496503/
https://www.ncbi.nlm.nih.gov/pubmed/28717457
http://dx.doi.org/10.1039/c5sc00051c
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author Holthausen, Michael H.
Hiranandani, Rashi R.
Stephan, Douglas W.
author_facet Holthausen, Michael H.
Hiranandani, Rashi R.
Stephan, Douglas W.
author_sort Holthausen, Michael H.
collection PubMed
description Stepwise oxidation of 1,8-bis(diphenylphosphino)naphthalene and a series of (oligo)methylene-linked diphosphines with XeF(2) followed by fluoride abstraction yields a family of compounds featuring phosphine, phosphonium and phosphorane moieties in close proximity. The bisphosphonium ions [(C(10)H(6))(Ph(2)PF)(2)](2+) (5) and [CH(2)(Ph(2)PF)(2)](2+) (9a) exhibit remarkable Lewis acidity arising from the proximity of the phosphonium centers. The effectiveness of bisphosphonium dications (5, 9a–e) is examined in a series of Lewis acid catalysed transformations.
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spelling pubmed-54965032017-07-17 Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines Holthausen, Michael H. Hiranandani, Rashi R. Stephan, Douglas W. Chem Sci Chemistry Stepwise oxidation of 1,8-bis(diphenylphosphino)naphthalene and a series of (oligo)methylene-linked diphosphines with XeF(2) followed by fluoride abstraction yields a family of compounds featuring phosphine, phosphonium and phosphorane moieties in close proximity. The bisphosphonium ions [(C(10)H(6))(Ph(2)PF)(2)](2+) (5) and [CH(2)(Ph(2)PF)(2)](2+) (9a) exhibit remarkable Lewis acidity arising from the proximity of the phosphonium centers. The effectiveness of bisphosphonium dications (5, 9a–e) is examined in a series of Lewis acid catalysed transformations. Royal Society of Chemistry 2015-03-01 2015-01-27 /pmc/articles/PMC5496503/ /pubmed/28717457 http://dx.doi.org/10.1039/c5sc00051c Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Holthausen, Michael H.
Hiranandani, Rashi R.
Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
title Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
title_full Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
title_fullStr Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
title_full_unstemmed Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
title_short Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
title_sort electrophilic bis-fluorophosphonium dications: lewis acid catalysts from diphosphines
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496503/
https://www.ncbi.nlm.nih.gov/pubmed/28717457
http://dx.doi.org/10.1039/c5sc00051c
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