Diphosphaenones: beyond the phosphorus analogue of enones†
Abstract
Phosphaenones, like their carbon analogue enones (CC–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