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Updated: Jul 5, 2025

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
Access to ligand-stabilized PH-containing phosphenium complexes
David Biskup1, Gregor Schnakenburg1, Arturo Espinosa Ferao2
1Institut für Anorganische Chemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhard-Domagk-Str. 1, 53121 Bonn, Germany. r.streubel@uni-bonn.de.
Abstract:
While the chemistry of phosphenium compounds, including metal complexes thereof, is very well established, few derivatives having a P-H bond have been described, yet. This work describes rational access to donor-stabilised phosphenium metal complexes possessing a P-H bond using protonation reactions of stable phosphinidene complex adducts. While most Brønsted-Lowry acids yield formal 1,1-addition products at the phosphorus centre under the loss of the donor, super-strong acids having weakly coordinating anions enable access to donor-stabilised P-H phosphenium complex salts. The latter possess N-methylimidazole as a donor (to phosphorus) and the N-P interaction has been studied theoretically.
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