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We report the isolation and characterization of a singlet organophosphinidene, suggesting new insights into phosphinidene behavior.
We report the isolation and characterization of a singlet organophosphinidene supported by a rigid 1,8-disubstituted anthracenyl group. This ligand scaffold weakly stabilizes the P(+1) state through weak, ultralong intramolecular P···N interactions among the two flanking amines and the central P atom. The electronic structure and phosphinidene nature of the compound are described by an in-depth computational analysis and targeted reactivity studies, which reveal behavior closely analogous to that of singlet phosphinidene sources.
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Bourque et al. (2026) studied this question.
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