Literature DB >> 25785571

Synthesis and Lewis acidity of fluorophosphonium cations.

Christopher B Caputo1, Daniel Winkelhaus, Roman Dobrovetsky, Lindsay J Hounjet, Douglas W Stephan.   

Abstract

A series of fluorophosphonium salts, [R3PF][X] (R = alkyl or aryl; X = FB(C6F5)3, [B(C6F5)4]), have been prepared by reactions of phosphine/borane frustrated Lewis pairs (FLPs) with XeF2 or difluorophosphoranes with [Et3Si][B(C6F5)4]. As the substituents bound to phosphorus become increasingly electron withdrawing, the corresponding fluorophosphonium salts are shown to be increasingly Lewis acidic. Calculations were also performed to determine the relative fluoride ion affinities (FIA) of these fluorophosphonium cations.

Entities:  

Year:  2015        PMID: 25785571     DOI: 10.1039/c5dt00217f

Source DB:  PubMed          Journal:  Dalton Trans        ISSN: 1477-9226            Impact factor:   4.390


  4 in total

1.  Carbodiphosphorane mediated synthesis of a triflyloxyphosphonium dication and its reactivity towards nucleophiles.

Authors:  S Yogendra; F Hennersdorf; A Bauzá; A Frontera; R Fischer; J J Weigand
Journal:  Chem Commun (Camb)       Date:  2017-03-07       Impact factor: 6.222

2.  Heterolytic Si-H Bond Cleavage at a Molybdenum-Oxido-Based Lewis Pair.

Authors:  Niklas Zwettler; Simon P Walg; Ferdinand Belaj; Nadia C Mösch-Zanetti
Journal:  Chemistry       Date:  2018-04-27       Impact factor: 5.236

3.  Phosphine and carbene azido-cations: [(L)N3]+ and [(L)2N3].

Authors:  Daniel Winkelhaus; Michael H Holthausen; Roman Dobrovetsky; Douglas W Stephan
Journal:  Chem Sci       Date:  2015-07-21       Impact factor: 9.825

4.  Synthesis and Structure of Mono-, Di-, and Trinuclear Fluorotriarylbismuthonium Cations.

Authors:  Jennifer Kuziola; Marc Magre; Nils Nöthling; Josep Cornella
Journal:  Organometallics       Date:  2022-05-09       Impact factor: 3.837

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.