Issue 14, 2024

Sequential radical and cationic reactivity at separated sites within one molecule in solution

Abstract

Distonic radical cations (DRCs) with spatially separated charge and radical sites are expected to show both radical and cationic reactivity at different sites within one molecule. However, such “dual” reactivity has rarely been observed in the condensed phase. Herein we report the isolation of crystalline 1λ2,3λ2-1-phosphonia-3-phosphinyl-cyclohex-4-enes 2a,b˙+, which can be considered delocalized DRCs and were completely characterized by crystallographic, spectroscopic, and computational methods. These DRCs contain a radical and cationic site with seven and six valence electrons, respectively, which are both stabilized via conjugation, yet remain spatially separated. They exhibit reactivity that differs from that of conventional radical cations (CRCs); specifically they show sequential radical and cationic reactivity at separated sites within one molecule in solution.

Graphical abstract: Sequential radical and cationic reactivity at separated sites within one molecule in solution

Supplementary files

Article information

Article type
Edge Article
Submitted
10 Jan 2024
Accepted
29 Feb 2024
First published
01 Mar 2024
This article is Open Access

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

Chem. Sci., 2024,15, 5376-5384

Sequential radical and cationic reactivity at separated sites within one molecule in solution

S. Liu, Y. Li, J. Lin, Z. Ke, H. Grützmacher, C. Su and Z. Li, Chem. Sci., 2024, 15, 5376 DOI: 10.1039/D4SC00201F

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