Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9577580 | Chemical Physics Letters | 2005 | 6 Pages |
Abstract
Solvent-dependent intra- and intermolecular vibrational energy transfer from the triply degenerate CO stretch mode of W(CO)6 is observed in nine alkanes (CnH2n + 2, n = 5-13) with single-color sub-picosecond time-resolved infrared spectroscopy. In all the solvents, the vibrational relaxation process is well characterized by three time constants: Ï1 (<1 ps), Ï2 (3-13 ps) and Ï3 (124-160 ps). The solvent dependence of Ï2 and Ï3 cannot be explained by the macroscopic properties of the solvent. In particular, the longest time constant Ï3 shows the minimum value of 124 ps in decane among the nine alkanes. The rate of the vibrational energy relaxation is a sensitive measure of the microscopic environments.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Motohiro Banno, Shin Sato, Koichi Iwata, Hiro-o Hamaguchi,