Reactivity of Diaryl Bismuth Cations toward a Platinum(0) Complex: Oxidative Aryl Transfer

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Authors: Johannes Schwarzmann, Cissie Slopianka, Crispin Lichtenberg
Cited by: 2
References: 85

Abstract

High Resolution Image Download MS PowerPoint Slide Reactions of three aryl-substituted bismuth cations, [BiPh 2 (SbF 6 )], [BiMes 2 (SbF 6 )], and [BiDipp 2 (SbF 6 )], with the Pt 0 complex Pt(PCy 3 ) 2 have been investigated (Mes = 2,4,6-trimethyl-phenyl; Dipp = 2,6-di- iso -propyl-phenyl; Cy = cyclohexyl). Unexpectedly, and in contrast with the reactivity of the recently reported methyl analogue [BiMe 2 (SbF 6 )], the formation of isolable metal-only Lewis pairs [(Cy 3 P) 2 Pt→BiAr 2 (SbF 6 )] is not observed (Ar = aryl). Instead, an unprecedented bismuth-to-platinum oxidative aryl transfer is witnessed to give the Pt II complexes [PtAr(PCy 3 ) 2 (SbF 6 )], along with the suggested bismuthinidene intermediates BiAr. Attempts to trap these fleeting intermediates with an ortho -quinone led to a Pt II semiquinone radical complex.

Fields of Study & Subjects

Synthesis and characterization of novel inorganic/organometallic compounds Organometallic Complex Synthesis and Catalysis Organoboron and organosilicon chemistry

Publication details

Journal / source
Organometallics
Publisher
American Chemical Society (ACS)
Volume
45
Issue
2
Pages
188–196
Publication date
6 January 2026
Language
EN