Solvation dynamics and rotation of coumarin 153 in alkylphosphonium ionic liquids

被引:233
作者
Ito, N
Arzhantsev, S
Heitz, M
Maroncelli, M [1 ]
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] SUNY Coll Brockport, Dept Chem, Brockport, NY 14420 USA
关键词
D O I
10.1021/jp0499575
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
Solvation and rotational dynamics of coumarin 153 (C153) were measured in a series of phosphonium ionic liquids consisting of the trihexyl(tetradecyl)phosphonium cation and the anions Br-, Cl-, dicyanamide(-), bis(trifluoromethylsulfonyl)imide(-), and BF4-. None of these liquids display a prominent ultrafast solvation component comparable to the one observed in imidizalium ionic liquids. The solvation dynamics observed on the nanosecond time scale are also 5-fold slower than those in imidazolium liquids of comparable viscosities. Both rotation and solvation are highly nonexponential functions of time and can be represented by stretched-exponential decays with exponents near 0.5. Characteristic times of these processes track solvent viscosity. A number of similarities between the dynamics observed in these ionic liquids and supercooled glass-forming liquids are noted.
引用
收藏
页码:5771 / 5777
页数:7
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