Issue 53, 2022

Photoactivation of triosmium dodecacarbonyl at 400 nm probed with time-resolved X-ray liquidography

Abstract

The photoactivation mechanism of Os3(CO)12 at 400 nm is examined with time-resolved X-ray liquidography. The data reveal two pathways: the vibrational relaxation following an internal conversion to the electronic ground state and the ligand dissociation to form Os3(CO)11 with a ligand vacancy at the axial position.

Graphical abstract: Photoactivation of triosmium dodecacarbonyl at 400 nm probed with time-resolved X-ray liquidography

Supplementary files

Article information

Article type
Communication
Submitted
02 May 2022
Accepted
07 Jun 2022
First published
08 Jun 2022
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2022,58, 7380-7383

Photoactivation of triosmium dodecacarbonyl at 400 nm probed with time-resolved X-ray liquidography

H. Ki, T. W. Kim, J. Moon, J. Kim, Y. Lee, J. Heo, K. H. Kim, Q. Kong, D. Khakhulin, G. Newby, J. Kim, J. Kim, M. Wulff and H. Ihee, Chem. Commun., 2022, 58, 7380 DOI: 10.1039/D2CC02438A

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