Journal
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Volume 325, Issue -, Pages 13-21Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2016.03.027
Keywords
Photosolvation; Chain photochemical processes; Primary photochemical process; Electron transfer; Hexachloroplatinate(IV); Laser flash photolysis; Ultrafast kinetic spectroscopy
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Funding
- Russian Science Foundation [15-13-10012]
- Russian Science Foundation [15-13-10012] Funding Source: Russian Science Foundation
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Photosolvation of hexachloroplatinate(IV) in acetonitrile with the formation of the (PtCl5)-Cl-IV(CH3CN)(-) complex was studied in the time range from hundreds of femtoseconds to seconds. The primary Pt(III) intermediate was recorded and interpreted as the primary Adamson radical pair [(PtCl52-)-Cl-III(C-4v)center dot center dot center dot Cl-center dot], which then accepts an electron from a solvent molecule. Two successive Pt(III) intermediates recorded in time range from microseconds to tens of milliseconds were interpreted as (PtCl52-)-Cl-III(C-4V) and (PtCl4-)-Cl-III complexes. (PtCl4-)-Cl-III was proposed to be a chain carrier in the chain photosolvation process. Dependencies of quantum yield of photosolvation on the initial complex concentration and excited light intensity were fitted in the framework of the proposed chain mechanism. Rate constants of the reactions of intermediates were determined. (C) 2016 Elsevier B.V. All rights reserved.
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