Solvation dynamics in the water pool of an aerosol-OT microemulsion. Effect of sodium salicylate and sodium cholate

被引:54
作者
Dutta, P [1 ]
Sen, P [1 ]
Mukherjee, S [1 ]
Halder, A [1 ]
Bhattacharyya, K [1 ]
机构
[1] Indian Assoc Cultivat Sci, Dept Chem Phys, Kolkata 700032, W Bengal, India
关键词
D O I
10.1021/jp030083g
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
The effect of sodium salicylate (Na-sal) and sodium cholate (Na-cholate) on the solvation dynamics in the water pool of aerosol-OT (AOT, sodium dioctylsulfosuccinate) microemulsion in n-heptane is reported. In the absence of any additive, the solvation dynamics of 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran (DCM) in AOT microemulsions is found to be biexponential with an average solvation time (tau(s)) of 710 ps. In the water pool, <tau(s)> decreases to 330 ps on addition of 1 mM Na-sal and increases to 3050 ps in the presence of 100 mM Na-cholate. The spectral width (F) of the time-resolved emission spectra of DCM in the water pool is found to be time dependent. This is ascribed to diffusion of the probe (DCM). The Na-sal-induced acceleration of the solvation dynamics is ascribed to the increase in the size of the water pool. In bulk water, in the presence of 100 mM Na-cholate (a bile salt), (tau(s)) is similar to830 ps. This is 4 times shorter than T, in the presence of Na-cholate in the water pool. This is ascribed to extreme crowding in the water pool because of the presence of Na-cholate aggregates. In bulk water, the emission spectral width displays a very small time dependence in the presence of Na-cholate aggregates. This suggests that in this case self-diffusion is unimportant and the slow solvation arises entirely from the dynamic exchange.
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页码:10815 / 10822
页数:8
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