Issue 3, 2015

Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines

Abstract

Stepwise oxidation of 1,8-bis(diphenylphosphino)naphthalene and a series of (oligo)methylene-linked diphosphines with XeF2 followed by fluoride abstraction yields a family of compounds featuring phosphine, phosphonium and phosphorane moieties in close proximity. The bisphosphonium ions [(C10H6)(Ph2PF)2]2+ (5) and [CH2(Ph2PF)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.

Graphical abstract: Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines

Supplementary files

Article information

Article type
Edge Article
Submitted
06 Jan 2015
Accepted
27 Jan 2015
First published
27 Jan 2015
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2015,6, 2016-2021

Author version available

Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines

M. H. Holthausen, R. R. Hiranandani and D. W. Stephan, Chem. Sci., 2015, 6, 2016 DOI: 10.1039/C5SC00051C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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