STUDY ON VIBRATIONAL RELAXATION DYNAMICS OF PHENOL-WATER COMPLEX BY PICOSECOND TIME-RESOLVED IR-UV PUMP-PROBE SPECTROSCOPY IN A SUPERSONIC MOLECULAR BEAM

Chemical physics Volume 419 Page 205-211 published_at 2013-06-20
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Title ( eng )
STUDY ON VIBRATIONAL RELAXATION DYNAMICS OF PHENOL-WATER COMPLEX BY PICOSECOND TIME-RESOLVED IR-UV PUMP-PROBE SPECTROSCOPY IN A SUPERSONIC MOLECULAR BEAM
Creator
Miyazaki Yasunori
Petković Milena
Source Title
Chemical physics
Volume 419
Start Page 205
End Page 211
Abstract
A comparative study of vibrational energy relaxation (VER) between the monohydrated complexes of phenol-d0 and phenol-d1 is investigated in a supersonic molecular beam. The direct time-resolved measurement of energy redistribution from the phenolic OH/OD stretching mode of the phenol-d0-H2O/phenol-d1-D2O is performed by picosecond IR-UV pump-probe spectroscopy. Two complexes follow the same relaxation process that begins with the intramolecular vibrational energy redistribution (IVR) and the intermolecular vibrational energy redistribution (IVR), which is followed by the vibrational predissociation (VP). The difference in the relaxation lifetimes between them is discussed by anharmonic force field and RRKM calculations. Anharmonic analysis implies that intra- (IVR) and intermolecular (IVR) relaxations occur in parallel in the complexes. The RRKM-predicted dissociation (VP) lifetimes show qualitative agreement with the observed results, suggesting that VP takes place after the statistical energy distribution in the complexes.
Descriptions
This work is supported by MEXT for the Scientific Research on Priority Area “Molecular Science for Supra Functional Systems” (No. 477).
This is a postprint of an article published by Elsevier B.V. in Chemical physics, 2013, available online: http://www.sciencedirect.com/science/article/pii/S0301010413001201
NDC
Chemistry [ 430 ]
Language
eng
Resource Type journal article
Publisher
Elsevier B.V.
Date of Issued 2013-06-20
Rights
Copyright (c) 2013 Elsevier B.V.
Publish Type Author’s Original
Access Rights open access
Source Identifier
[ISSN] 0301-0104
[NCID] AA00602111
[DOI] 10.1016/j.chemphys.2013.02.023
[DOI] http://dx.doi.org/10.1016/j.chemphys.2013.02.023 isVersionOf