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Microscopic solvation environments in a prototype room-temperature ionic liquid as elucidated by resonance Raman spectroscopy of iodine and bromine.
Saha, Satyen; Okajima, Hajime; Homma, Osamu; Hamaguchi, Hiro-O.
Afiliação
  • Saha S; Department of Chemistry, Centre for Advanced Studies, Institute of Science, Banaras Hindu University, Varanasi 221005, India.
  • Okajima H; Institute of Molecular Science, National Chiao Tung University, 1001 Ta Hsueh Road, Hsinchu 300, Taiwan.
  • Homma O; Department of Chemistry, School of Science, The University of Tokyo, Hongo 7-3-1 Bunkyo-ku, Tokyo, 113-0033, Japan.
  • Hamaguchi HO; Institute of Molecular Science, National Chiao Tung University, 1001 Ta Hsueh Road, Hsinchu 300, Taiwan; Department of Chemistry, School of Science, The University of Tokyo, Hongo 7-3-1 Bunkyo-ku, Tokyo, 113-0033, Japan. Electronic address: hhama@chem.s.u-tokyo.ac.jp.
Article em En | MEDLINE | ID: mdl-28076768
ABSTRACT
Microscopic solvation environments in a prototype ionic liquid, bmimTf2N; 1-butyl-3-methyl-imidazolium-bis(trifluoromethanesulfonyl)imide, have been studied with the use of halides, X2 and Xn- (X=I, Br; n=3,5), as molecular probes. Resonance Raman spectroscopy has been used to detect these halogen species existing in bmimTf2N as well as in reference solvents including heptane, cyclohexane, KX/H2O and benzene. In heptane and cyclohexane, only free X2 species are detected. In KX/H2O, only Xn- and, in benzene, only benzene-X2 complexes are detected. On the contrary, free X2 and Xn- are concomitantly detected in bmimTf2N, indicating that there are two distinct solvation environments in bmimTf2N, non-polar environments that solvate free X2 and polar environments that stabilize Xn-. These two distinct solvation environments are most likely to arise from microscopic structural heterogeneity of ionic liquids.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article