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

Author:

Ki Hosung12,Kim Tae Wu3ORCID,Moon Jiwon4,Kim Jungmin12,Lee Yunbeom12,Heo Jun12,Kim Kyung Hwan5,Kong Qingyu6,Khakhulin Dmitry7,Newby Gemma8,Kim Joonghan4ORCID,Kim Jeongho9ORCID,Wulff Michael8,Ihee Hyotcherl12ORCID

Affiliation:

1. Center for Advanced Reaction Dynamics, Institute for Basic Science (IBS), Daejeon 34141, Republic of Korea

2. Department of Chemistry and KI for the BioCentury, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea

3. Department of Chemistry, Mokpo National University, Muan-gun, Jeollanam-do 58554, Republic of Korea

4. Department of Chemistry, The Catholic University of Korea, Bucheon 14662, Republic of Korea

5. Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea

6. Synchrotron Soleil, L’Orme des Merisiers, Saint-Aubin, BP 48, 91192 Gif-sur-Yvette Cedex, France

7. European XFEL, Holzkoppel 4, 22869 Schenefeld, Germany

8. European Synchrotron Radiation Facility, BP 220, 38043 Grenoble Cedex, France

9. Department of Chemistry, Inha University, Incheon 22212, Republic of Korea

Abstract

Photoactivation mechanism of triosmium dodecacarbonyl is elucidated via time-resolved X-ray liquidography, identifying two pathways, vibrational relaxation and ligand dissociation.

Funder

Institute for Basic Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

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