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Vibrational coherence transfer in the ultrafast intersystem crossing of a diplatinum complex in solution
- 1.0490769 - ÚFCH JH 2019 RIV US eng J - Článek v odborném periodiku
Monni, R. - Capano, G. - Auböck, G. - Gray, H. B. - Vlček, Antonín - Tavernelli, I.
Vibrational coherence transfer in the ultrafast intersystem crossing of a diplatinum complex in solution.
Proceedings of the National Academy of Sciences of the United States of America. Roč. 115, č. 28 (2018), E6396-E6403. ISSN 0027-8424. E-ISSN 1091-6490
Grant CEP: GA ČR GA17-01137S
Grant ostatní: COST(XE) CM1202; COST(XE) CM1405
Institucionální podpora: RVO:61388955
Klíčová slova: ultrafast * intersystem crossing * vibrational coherence
Obor OECD: Physical chemistry
Impakt faktor: 9.580, rok: 2018
Způsob publikování: Open access
We investigate the ultrafast transient absorption response of tetrakis(mu-pyrophosphito) diplatinate(II), [Pt-2(mu-P2O5H2)(4)](4-) [hereafter abbreviated Pt(pop)], in acetonitrile upon excitation of its lowest singlet (1)A(2u) state. Compared with previously reported solvents [van der Veen RM, Cannizzo A, vanMourik F, Vlcek A, Jr, CherguiM(2011) J Am Chem Soc 133:305-315], a significant shortening of the intersystem crossing (ISC) time (<1 ps) from the lowest singlet to the lowest triplet state is found, allowing for a transfer of vibrational coherence, observed in the course of an ISC in a polyatomic molecule in solution. Density functional theory (DFT) quantum mechanical/molecular mechanical (QM/MM) simulations of Pt( pop) in acetonitrile and ethanol show that high-lying, mostly triplet, states are strongly mixed and shifted to lower energies due to interactions with the solvent, providing an intermediate state (or manifold of states) for the ISC. This suggests that the larger the solvation energies of the intermediate state(s), the shorter the ISC time. Because the latter is smaller than the pure dephasing time of the vibrational wave packet, coherence is conserved during the spin transition. These results underscore the crucial role of the solvent in directing pathways of intramolecular energy flow.
Trvalý link: http://hdl.handle.net/11104/0285564
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