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室温离子液体中二碘阴离子自由基的扩散系数和双分子反应速率的电荷效应

Charge effect on the diffusion coefficient and the bimolecular reaction rate of diiodide anion radical in room temperature ionic liquids.

作者信息

Nishiyama Yoshio, Terazima Masahide, Kimura Yoshifumi

机构信息

Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.

出版信息

J Phys Chem B. 2009 Apr 16;113(15):5188-93. doi: 10.1021/jp811306b.

Abstract

The diffusion coefficients of diiodide anion radical, I(2)(-), in room temperature ionic liquids (RTILs) were determined by the transient grating (TG) method using the photochemical reaction of iodide. The diffusion coefficients we obtained were larger in RTILs than the theoretical predictions by the Stokes-Einstein relation, whereas both values are similar in conventional solvents. By comparison with the diffusion coefficients of neutral molecules, it was suggested that the Coulomb interaction between I(2)(-) and constituent ions of RTILs strongly affects the diffusion coefficients. The bimolecular reaction rates between I(2)(-) were calculated by the Debye-Smoluchowski equation using the experimentally determined diffusion coefficients. These calculated reaction rate were much smaller than the experimentally determined rates (Takahashi, K.; et al. J. Phys. Chem. B 2007, 111, 4807), indicating the charge screening effect of RTILs.

摘要

通过碘化物的光化学反应,采用瞬态光栅(TG)法测定了二碘阴离子自由基I₂⁻在室温离子液体(RTILs)中的扩散系数。我们得到的扩散系数在RTILs中比通过斯托克斯-爱因斯坦关系的理论预测值要大,而在传统溶剂中这两个值相似。通过与中性分子的扩散系数比较,表明I₂⁻与RTILs的组成离子之间的库仑相互作用强烈影响扩散系数。使用实验测定的扩散系数,通过德拜-斯莫卢霍夫斯基方程计算了I₂⁻之间的双分子反应速率。这些计算得到的反应速率比实验测定的速率小得多(高桥,K.等人,《物理化学杂志B》,2007年,111卷,4807页),表明RTILs的电荷屏蔽效应。

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