Issue 47, 2022

Bisstibane–distibane conversion via consecutive single-electron oxidation and reduction reaction

Abstract

peri-Substituted naphthalene complexes (Trip2Pn)2Naph (Pn = Sb 1, Bi 2) were synthesised and their redox behaviour investigated. Oxidation of 1 with [Fc][BArF] (BArF = B(C6F5)4) yielded [(Trip2Sb)(TripSb)Naph][BArF] (3) containing the stibane-coordinated stibenium cation [(Trip2Sb)(TripSb)Naph]+. Subsequent reduction of 3 with KC8 yielded distibane (TripSb)2Naph (4). 1–4 were characterised by NMR (1H, 13C) and IR spectroscopy as well as single-crystal X-ray diffraction (sc-XRD), while their electronic structures were analysed by quantum chemical computations.

Graphical abstract: Bisstibane–distibane conversion via consecutive single-electron oxidation and reduction reaction

Supplementary files

Article information

Article type
Communication
Submitted
07 Apr 2022
Accepted
10 May 2022
First published
12 May 2022
This article is Open Access
Creative Commons BY license

Chem. Commun., 2022,58, 6682-6685

Bisstibane–distibane conversion via consecutive single-electron oxidation and reduction reaction

A. Gehlhaar, H. M. Weinert, C. Wölper, N. Semleit, G. Haberhauer and S. Schulz, Chem. Commun., 2022, 58, 6682 DOI: 10.1039/D2CC01986H

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