Solvation of α-hydroxydiphenylmethyl radical in room temperature ionic liquids studied by transient FT-EPR spectroscopy

被引:31
作者
Kawai, A [1 ]
Hidemori, T [1 ]
Shibuya, K [1 ]
机构
[1] Tokyo Inst Technol, Grad Sch Sci & Engn, Dept Chem, Meguro Ku, Tokyo 1528551, Japan
关键词
D O I
10.1016/j.cplett.2005.08.030
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
To understand solvation in room temperature ionic liquids (RTILs), an FT-EPR spectrum of alpha-hydroxydiphenylmethyl (HDPM) radical was measured in several RTILs of tert-alkylammonium or alkylimidazolium salts with anions of PF6-, BF4- (CF3SO2)(2)N-, CF3SO3-, WO42-, Cl- and Br-. The hyperfine coupling constant of the hydroxyl proton depends on Gutmann's donor number of the anion S, while the constants of phenyl alpha-protons are essentially the same for these RTILs. This result suggests the electron donor character of anions is important in HDPM solvation in RTILs through the anion-OH group hydrogen-bond. (c) 2005 Elsevier B.V.. All rights reserved.
引用
收藏
页码:378 / 383
页数:6
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