Time-resolved laser spectroscopy of nonreactive processes in ionic liquids and their binary mixtures with organic solvents and CO2

被引:3
作者
Ernsting, N. P. [1 ]
Lenzer, T. [2 ]
Oum, K. [2 ]
机构
[1] Humboldt Univ, Inst Chem, D-12489 Berlin, Germany
[2] Univ Siegen, D-57076 Siegen, Germany
关键词
Ionic liquids; Time-resolved laser spectroscopy; Solvation dynamics; Polarity; COMPLETE SOLVATION RESPONSE; INTERNAL-CONVERSION LIFETIME; STATIC DIELECTRIC-CONSTANT; ULTRAFAST SOLVATION; GRATING TECHNIQUE; COUMARIN; 153; DYNAMICS; TEMPERATURE; RELAXATION; POLARITY;
D O I
10.1016/j.molliq.2013.08.010
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
Nonreactive dynamics of molecules in ionic liquids (ILs) have been investigated in various environments, such as in neat aprotic and protic ILs, as well as in binary mixtures of ILs with polar organic solvents and CO2. Transient broadband absorption and fluorescence spectroscopic techniques on timescales from femto-seconds to milliseconds have been applied to elucidate the importance of different types of solute-solvent interactions in these media. Molecular probes such a 12 '-apo-beta-carotenoic-12 '-acid and Coumarin C153 have been used as reporter molecules for ionic liquid solvation dynamics, micropolarity, hydrogen-bonding and collisional relaxation. With Coumarin C153 in ILs, the relationship between the complete salvation response and microwave-terahertz absorption measurements of the neat liquid was explored quantitatively. A reduced value for the conductivity plays a key role in such salvation experiments. Aprotic ILs exhibit a micropolarity larger than expected from their static dielectric constants, whereas the local polarity of protic alkylammonium formate ILs appears to be similar to that of alcohols having comparable dielectric constants. In IL mixtures with organic solvents or CO2, there is no indication for differences in the bulk composition and the local composition around the molecular probe. Collisional relaxation processes in ILs take place on similar timescales as in dipolar organic solvents. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 93
页数:7
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