Ultrafast solvation dynamics and charge transfer reactions in room temperature ionic liquids

被引:37
作者
Nagasawa, Yutaka [1 ,2 ,3 ]
Miyasaka, Hiroshi [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Div Frontier Mat Sci, Toyonaka, Osaka 5608531, Japan
[2] Osaka Univ, Ctr Quantum Sci & Technol Extreme Condit, Toyonaka, Osaka 5608531, Japan
[3] Japan Sci & Technol Agcy JST, PRESTO, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
INTRAMOLECULAR ELECTRON-TRANSFER; ECHO PEAK SHIFT; WAVELENGTH-DEPENDENT FLUORESCENCE; KERR-EFFECT SPECTRA; SOLUTE-SOLVENT INTERACTION; PROTON-TRANSFER REACTION; EXCITED-STATE DYNAMICS; ALKYL CHAIN-LENGTH; MOLECULAR-DYNAMICS; PHOTON-ECHO;
D O I
10.1039/c3cp55465a
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
Room temperature ionic liquids (ILs) are a new type of solvent with peculiar properties. ILs are usually composed of an anion and a bulky cation with one or more alkyl chains to decrease the melting point. These structural peculiarities lead to the high viscosity and the heterogeneity of ILs, which could affect chemical reactions. In the present perspective, we will first introduce the experimentally observed nature of the heterogeneous liquid structure and then introduce recent developments in the study on electron transfer (ET) and charge transfer (CT) reactions in relation with the solvation and the heterogeneity of ILs. Because of the high viscosity of ILs, diffusive solvation is expected to be slow which could be the rate-limiting factor for ET and CT processes. However, ILs could provide a unique reaction field depending on the location of the solute within the heterogeneous liquid structure and the reaction could be faster than that expected from the bulk viscosity due to the fast fluctuation of the local environment.
引用
收藏
页码:13008 / 13026
页数:19
相关论文
共 208 条
[1]   Three pulse photon echo peak shift study of the B800 band of the LH2 complex of Rps. acidophila at room temperature:: A coupled master equation and nonlinear optical response function approach [J].
Agarwal, R ;
Yang, M ;
Xu, QH ;
Fleming, GR .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (09) :1887-1894
[2]   PICOSECOND EXCITED-STATE SOLVATION DYNAMICS OF 9,9'-BIANTHRYL IN ALCOHOL-SOLUTIONS [J].
ANTHON, DW ;
CLARK, JH .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (13) :3530-3536
[3]   Ionic liquids for the convenient synthesis of functional nanoparticles and other inorganic nanostructures [J].
Antonietti, M ;
Kuang, DB ;
Smarsly, B ;
Yong, Z .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (38) :4988-4992
[4]  
Armand M, 2009, NAT MATER, V8, P621, DOI [10.1038/NMAT2448, 10.1038/nmat2448]
[5]   Observing the complete solvation response of DCS in imidazolium. ionic liquids, from the femtosecond to nanosecond regimes [J].
Arzhantsev, S ;
Jin, H ;
Ito, N ;
Maroncelli, M .
CHEMICAL PHYSICS LETTERS, 2006, 417 (4-6) :524-529
[6]   Solvation dynamics of coumarin 153 in several classes of ionic liquids: cation dependence of the ultrafast component [J].
Arzhantsev, S ;
Ito, N ;
Heitz, M ;
Maroncelli, M .
CHEMICAL PHYSICS LETTERS, 2003, 381 (3-4) :278-286
[7]   Measurements of the complete solvation response in ionic liquids [J].
Arzhantsev, Sergei ;
Jin, Hui ;
Baker, Gary A. ;
Maroncelli, Mark .
JOURNAL OF PHYSICAL CHEMISTRY B, 2007, 111 (18) :4978-4989
[8]   The smallest amphiphiles: Nanostructure in protic room-temperature ionic liquids with short alkyl groups [J].
Atkin, Rob ;
Warr, Gregory G. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (14) :4164-4166
[9]   Structure in confined room-temperature ionic liquids [J].
Atkin, Rob ;
Warr, Gregory G. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (13) :5162-5168
[10]   An in situ STM/AFM and impedance spectroscopy study of the extremely pure 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl) trifluorophosphate/Au(111) interface: potential dependent solvation layers and the herringbone reconstruction [J].
Atkin, Rob ;
Borisenko, Natalia ;
Drueschler, Marcel ;
El Abedin, Sherif Zein ;
Endres, Frank ;
Hayes, Robert ;
Huber, Benedikt ;
Roling, Bernhard .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (15) :6849-6857