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Reversible cooperative dihydrogen binding and transfer with a bis-phosphenium complex of chromium
Authors:Nicholas Birchall  Christoph M Feil  Michael Gediga  Martin Nieger  Dietrich Gudat
Institution:Institute of Inorganic Chemistry, University of Stuttgart, Pfaffenwaldring 55, 70550 Stuttgart Germany.; Department of Chemistry, P.O. Box 55, 00014 University of Helsinki Finland
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 Created by potrace 1.16, written by Peter Selinger 2001-2019 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.

Photolysis of a phosphenium complex enables reversible activation of H2 to yield a dihydrogen complex which stimulates H2 cleavage or catalytic hydrogenation.
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