Diphosphaenones: beyond the phosphorus analogue of enones†
Abstract
Phosphaenones, like their carbon analogue enones (C
C–C
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
P–C(O)–NHV]. X-ray diffraction methods allowed determination of the structures, which show a central planar trans P
P–C
O configuration. Compound 3a behaves like classical enones and shows 1,4-addition across the P
P–C
O unit, which proceeds in a stepwise manner. In contrast, 3a exhibits also 1,2-addition across the P
P but not the C
O double bond, which differentiates it from enones.
- This article is part of the themed collection: Celebrating the 100th Anniversary of Sun Yat-Sen University

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