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MO: Fachverband Molekülphysik
MO 2: Photochemistry
MO 2.3: Vortrag
Montag, 6. März 2023, 11:30–11:45, F142
Ultrafast Photochemistry of Metallo-Nitrenes — •Markus Bauer1, Till Schmidt-Räntsch2, Luis Domenianni1, Sven Schneider2, and Peter Vöhringer1 — 1Clausius Institut für physikalische Chemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Deutschland — 2Institut für Anorganische Chemie, Georg-August-Universität Göttingen, Deutschland
Metallo-nitrenes, formed by the photochemical decomposition of metallo-azides, have recently shown to be promising complexes for chemical catalysis, specifically for nucleophilic metallo-nitrene C-H insertion.[1] The exact reaction pathways, as well as the electronic structures of intermediate species remain so far largely unknown.
In this work, the photochemistry of the square-planar [M(N3)(PNP)] (PNP=N(CHCHPtBu2)2, M=Pd, Pt) complexes after excitation with 320 nm light were investigated using ultrafast UV-pump mIR-probe and time resolved Fourier transform IR-spectroscopy.
The data reveal that dinitrogen cleavage from the photolabile azide group occurs from the triplet state on a time scale in excess of 1 ns. The quantum yield for nitrene formation depends on the nature of the metal.
[1] T. Schmidt-Räntsch, H. Verplancke, J. N. Lienert, S. Demeshko, M. Otte, G. P. Van Trieste, K. A. Reid, J. H. Reibenspies, D. C. Powers, M. C. Holthausen, S. Schneider, Angew. Chem. Int. Ed. 2022, 61, e202115626;