Probing the scale of local density augmentation in supercritical fluids: A picosecond rotational reorientation study

被引:58
作者
Heitz, MP [1 ]
Bright, FV [1 ]
机构
[1] SUNY BUFFALO,DEPT CHEM,BUFFALO,NY 14260
关键词
D O I
10.1021/jp953589a
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 report on the rotational reorientation kinetics of N,N '-bis-(2,5-tert-butylphenyl)-3,4,9,10-perylene- carboxodiimide (BTBP) in several liquids and in three supercritical fluids (fluoroform, carbon dioxide, and ethane). In liquids, BTBP follows near perfect Debye-Stokes-Einstein (DSE) behavior under sticky boundary conditions. However, in supercritical fluids the rotational dynamics of BTBP are distinctly different. In close proximity to the critical density (rho(I) approximate to 1), the recovered rotational reorientation times are up to 12-fold greater than predicted by simple DSE theory with sticky boundary conditions. Upon increasing the fluid density, the recovered rotational reorientation times steadily decrease until they fall within hydrodynamic predictions (i.e., DSE theory). This extraordinary behavior is explained in terms of local solute-fluid density augmentation which is a feature particular only to supercritical fluids. The local density augmentation surrounding the solute is quantified in several ways. By using a model recently developed by Anderton and Kauffman (J. Phys. Chem. 1995, 99, 13759), the local fluid density is found to exceed the bulk by up to 300%. Upon increasing the pressure and moving away from the high compressibility region we see that the extent of local density augmentation decreases to a value approaching the bulk density. In an alternative interpretation, we explain the observed rotational reorientation dynamics in terms of the size of the solute-fluid cluster. At low fluid density (near the critical density) the radius of the ''solute-fluid cluster'' is a factor of 2 greater than the solute alone. Again, as pressure is increased, there is a decrease in the cluster size and the radius of the reorienting species (BTBP + clustered fluid molecules) approaches the predicted value based on DSE theory using friction/boundary terms determined for BTBP in normal liquid solvents.
引用
收藏
页码:6889 / 6897
页数:9
相关论文
共 79 条
[1]   TEMPERATURE-DEPENDENT ROTATIONAL RELAXATION OF DIPHENYLBUTADIENE IN N-ALCOHOLS - A TEST OF THE QUASI-HYDRODYNAMIC FREE-SPACE MODEL [J].
ANDERTON, RM ;
KAUFFMAN, JF .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (47) :12117-12124
[2]   ROTATIONAL RELAXATION IN THE COMPRESSIBLE REGION OF CO2 - EVIDENCE FOR SOLUTE-INDUCED CLUSTERING IN SUPERCRITICAL-FLUID SOLUTIONS [J].
ANDERTON, RM ;
KAUFFMAN, JF .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (38) :13759-13762
[3]  
Beechem J. M., 2002, TOPICS FLUORESCENCE, P241, DOI DOI 10.1007/0-306-47058-6_5
[4]   THE SOLUTE SIZE EFFECT IN ROTATIONAL DIFFUSION EXPERIMENTS - A TEST OF MICROSCOPIC FRICTION THEORIES [J].
BENAMOTZ, D ;
DRAKE, JM .
JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (02) :1019-1029
[5]   MICROSCOPIC FRICTIONAL FORCES ON MOLECULAR-MOTION IN LIQUIDS - PICOSECOND ROTATIONAL DIFFUSION IN ALKANES AND ALCOHOLS [J].
BENAMOTZ, D ;
SCOTT, TW .
JOURNAL OF CHEMICAL PHYSICS, 1987, 87 (07) :3739-3748
[6]   SPECTROSCOPIC DETERMINATION OF SOLUTE FLUID CLUSTER SIZE IN SUPERCRITICAL N2O [J].
BETTS, TA ;
ZAGROBELNY, J ;
BRIGHT, FV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (21) :8163-8171
[7]  
BETTS TA, 1992, THESIS SUNY BUFFALO
[8]  
BETTS TA, 1991, J SUPERCRIT FLUID, V5, P48
[9]  
BETTS TA, 1990, APPL SPECTROSC, V44, P1190