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Updated: Nov 2, 2025

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
Reversible cooperative dihydrogen binding and transfer with a bis-phosphenium complex of chromium
Nicholas Birchall1, Christoph M Feil1, Michael Gediga1
1Institute of Inorganic Chemistry, University of Stuttgart Pfaffenwaldring 55 70550 Stuttgart Germany gudat@iac.uni-stuttgart.de.
Abstract:
The reversible reaction of H2 with a bis-phosphenium complex of chromium provides a rare example of 3d transition metal/phosphenium cooperativity. Photolysis induces the activation of H2 and yields a spectroscopically detectable phosphenium-stabilized (σ-H2)-complex, readily showing exchange with gaseous H2 and D2. Further reaction of this complex affords a phosphine-functionalized metal hydride, representing a unique example of reversible H2 cleavage across a 3d M[double bond, length as m-dash]P bond. The same species is also accessible via stepwise H+/H- transfer to the bis-phosphenium complex, and releases H2 upon heating or irradiation. Dihydrogen transfer from the H2-complex to styrene is exploited to demonstrate the first example of promoting hydrogenation with a phosphenium complex.
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