Relaxation dynamics of inhomogeneous spectral width in binary solvents studied by transient hole-burning spectroscopy

被引:42
作者
Nishiyama, K
Okada, T [1 ]
机构
[1] Osaka Univ, Dept Chem, Grad Sch Engn Sci, Osaka 5608531, Japan
[2] Osaka Univ, KYOKUGEN, Osaka 5608531, Japan
[3] Osaka Univ, Venture Business Lab, Osaka 5650871, Japan
关键词
D O I
10.1021/jp983025h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have performed transient hole-burning spectroscopy of cresyl violet in binary solvents of different polarity components in order to detect the relaxation of inhomogeneous spectral bandwidths (relaxation of dispersion around average energy) in addition to that of spectral peak shift (relaxation of average energy). We proposed in our previous paper (J. Phys. Chem. A 1997, 101, 5729) that the relaxation process of spectral width and that of average energy of the system should be characterized by different relaxation modes of solvent molecules. In the binary solvents a slow relaxation process was observed especially for the spectral width, which was assigned to the translational diffusion of polar component of solvent molecules. On the other hand, the relaxation of average energy was not effectively affected by the solvent mixing, which could be attributed mainly to fast relaxation processes, the libration and/or rotational diffusion of solvent molecules in the closest solvation shell. Even if the distribution of the solvent shell would be disturbed by the slower translational diffusion mode of polar solvent molecules, the average energy could be immediately compensated by the fast relaxation of solvent surroundings. The developments of the molecular theory on the translational dynamics should be necessary for essential understanding of the results obtained here.
引用
收藏
页码:9729 / 9733
页数:5
相关论文
共 30 条
[1]   THEORY OF THE TIME DEVELOPMENT OF THE STOKES SHIFT IN POLAR MEDIA [J].
BAGCHI, B ;
OXTOBY, DW ;
FLEMING, GR .
CHEMICAL PHYSICS, 1984, 86 (03) :257-267
[2]  
Barbara P. F., 1990, ADV PHOTOCHEM, V15, P1, DOI [DOI 10.1002/9780470133453.CHL, DOI 10.1103/PhysRevLett.88.158101]
[3]   Solvation dynamics in monohydroxy alcohols: Agreement between theory and different experiments [J].
Biswas, R ;
Nandi, N ;
Bagchi, B .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (15) :2968-2979
[4]   SOLVATION DYNAMICS FOR AN ION-PAIR IN A POLAR-SOLVENT - TIME-DEPENDENT FLUORESCENCE AND PHOTOCHEMICAL CHARGE-TRANSFER [J].
CARTER, EA ;
HYNES, JT .
JOURNAL OF CHEMICAL PHYSICS, 1991, 94 (09) :5961-5979
[5]   ULTRAFAST SOLVENT DYNAMICS - CONNECTION BETWEEN TIME RESOLVED FLUORESCENCE AND OPTICAL KERR MEASUREMENTS [J].
CHO, MH ;
ROSENTHAL, SJ ;
SCHERER, NF ;
ZIEGLER, LD ;
FLEMING, GR .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (07) :5033-5038
[6]   Interaction-site-model description of collective excitations in classical molecular fluids [J].
Chong, SH ;
Hirata, F .
PHYSICAL REVIEW E, 1998, 57 (02) :1691-1701
[7]   Solvation dynamics in mixtures of polar and nonpolar solvents [J].
Cichos, F ;
Willert, A ;
Rempel, U ;
vonBorczyskowski, C .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (44) :8179-8185
[8]   SPECTRAL HOLE BURNING IN LARGE MOLECULES PROBED WITH 10 FS OPTICAL PULSES [J].
CRUZ, CHB ;
FORK, RL ;
KNOX, WH ;
SHANK, CV .
CHEMICAL PHYSICS LETTERS, 1986, 132 (4-5) :341-344
[9]   Ion solvation dynamics in binary mixtures [J].
Day, TJF ;
Patey, GN .
JOURNAL OF CHEMICAL PHYSICS, 1997, 106 (07) :2782-2791
[10]  
Eyring H., 1980, Basic Chemical Kinetics