Issue 47, 2024

Diphosphaenones: beyond the phosphorus analogue of enones

Abstract

Phosphaenones, like their carbon analogue enones (C[double bond, length as m-dash]C–C[double bond, length as m-dash]O), are promising building blocks for synthetic chemistry and materials science. However, in contrast to the α- and β-phosphaenones, structurally and spectroscopically well-defined diphosphaenones (DPEs) are rare. In this study, we disclose the isolation and spectroscopic characterization of N-heterocyclic vinyl (NHV) substituted acyclic DPEs 3a,b [NHV–P[double bond, length as m-dash]P–C(O)–NHV]. X-ray diffraction methods allowed determination of the structures, which show a central planar trans P[double bond, length as m-dash]P–C[double bond, length as m-dash]O configuration. Compound 3a behaves like classical enones and shows 1,4-addition across the P[double bond, length as m-dash]P–C[double bond, length as m-dash]O unit, which proceeds in a stepwise manner. In contrast, 3a exhibits also 1,2-addition across the P[double bond, length as m-dash]P but not the C[double bond, length as m-dash]O double bond, which differentiates it from enones.

Graphical abstract: Diphosphaenones: beyond the phosphorus analogue of enones

Supplementary files

Article information

Article type
Edge Article
Submitted
24 Sept. 2024
Accepted
09 Nov. 2024
First published
11 Nov. 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, 20030-20038

Diphosphaenones: beyond the phosphorus analogue of enones

J. Lin, S. Liu, S. Zheng, H. Grützmacher, C. Su and Z. Li, Chem. Sci., 2024, 15, 20030 DOI: 10.1039/D4SC06462C

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