Three pulse photon echo studies of nondipolar solvation: Comparison with a viscoelastic model

被引:90
作者
Larsen, DS [1 ]
Ohta, K
Fleming, GR
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Berkeley, CA 94720 USA
关键词
D O I
10.1063/1.480240
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
Three pulse stimulated photon echo peak shift (3PEPS) measurements were used to probe the solvation of a quadrupolar solute in three room temperature nondipolar solvents; benzene, CCl4, and CS2, and the results were compared with those for two polar solvents, methanol and acetonitrile, and one weakly polar solvent, toluene. Our data reveal three distinct solvent dynamical time scales; a sub-100 fs ultrafast component attributed to inertial motions, a slow (similar to 2-3 ps) component attributed to structural relaxation, and an intermediate time scale (similar to 600 fs) of uncertain origin. The six solvents were chosen to reflect a range of possible interactions, but exhibit similar dynamics, suggesting that similar mechanisms may be at work or that different mechanisms may exist, but occur on similar time scales. A viscoelastic continuum solvation model proposed to describe nonpolar solvation [J. Phys. Chem. A 102, 17 (1998)] was used for a preliminary analysis of our data. (C) 1999 American Institute of Physics. [S0021-9606(99)50643-0].
引用
收藏
页码:8970 / 8979
页数:10
相关论文
共 76 条
[1]   On the validity of electrostatic linear response in polar solvents [J].
Aqvist, J ;
Hansson, T .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (22) :9512-9521
[2]   MOLECULAR THEORY OF NONPOLAR SOLVATION DYNAMICS [J].
BAGCHI, B .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (09) :6658-6664
[3]   COMPARISON OF A VISCOELASTIC THEORY OF SOLVATION DYNAMICS TO TIME-RESOLVED EXPERIMENTS IN A NONPOLAR SOLUTION [J].
BERG, M .
CHEMICAL PHYSICS LETTERS, 1994, 228 (4-5) :317-322
[4]   Viscoelastic continuum model of nonpolar solvation. 1. Implications for multiple time scales in liquid dynamics [J].
Berg, M .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (01) :17-30
[5]   Vibrational energy relaxation, nonpolar solvation dynamics and instantaneous normal modes: Role of binary interaction in the ultrafast response of a dense liquid [J].
Biswas, R ;
Bhattacharyya, S ;
Bagchi, B .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (12) :4963-4971
[6]   Molecular dynamics simulation study of polarizable solute solvation in water .1. Equilibrium solvent structure and solute rotational dynamics [J].
Bursulaya, BD ;
Zichi, DA ;
Kim, HJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (04) :1392-1405
[7]   ROLE OF SOLUTE ELECTRONIC POLARIZABILITY IN SOLVATION DYNAMICS [J].
BURSULAYA, BD ;
ZICHI, DA ;
KIM, HJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (25) :10069-10074
[8]   Solvent dynamics derived from optical Kerr effect, dielectric dispersion, and time-resolved Stokes shift measurements: An empirical comparison [J].
Castner, EW ;
Maroncelli, M .
JOURNAL OF MOLECULAR LIQUIDS, 1998, 77 (1-3) :1-36
[9]   DIELECTRIC-RELAXATION OF DIPOLAR LIQUIDS [J].
CHANDRA, A ;
WEI, DQ ;
PATEY, GN .
JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (03) :2068-2073
[10]   MICROSCOPIC THEORY OF SOLVATION DYNAMICS IN DIPOLAR LIQUIDS [J].
CHANDRA, A ;
WEI, DQ ;
PATEY, GN .
JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (07) :4926-4931