FT-Raman study of ionic interactions in lithium and silver tetrafluoroborate solutions in acrylonitrile

被引:46
作者
Alia, JM
Edwards, HGM
机构
[1] Univ Castilla La Mancha, Dept Quim Fis, EUITA, E-13071 Ciudad Real, Spain
[2] Univ Bradford, Dept Chem & Forens Sci, Bradford BD7 1DP, W Yorkshire, England
关键词
solvation; ionic pairing; FT-Raman spectroscopy; silver tetrafluoroborate; lithium tetrafluoroborate;
D O I
10.1023/A:1005144113352
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
Solutions of silver and lithium tetrafluoroborate in acrylonitrile, over a range of concentrations between 0.5 and 4 mol-kg(-1), have been studied by Fourier-transform Raman spectroscopy. The spectral regions studied include the solvent v(C drop N) fundamental and the anion B-F symmetric stretching band. In AgBF4 solutions the absence of ionic pairing was demonstrated and the anion v(1)(A(1)) remains as single narrow band located at 764.7+/-0.1 cm(-1). Consequently, the silver ion solvation number does not change in the range of concentrations studied, having a constant value of 3.54+/-0.10. However, a high level of ionic pairing was observed in the corresponding solutions of LiBF4. Three components were detected in the tetrafluoroborate v(1)(A(1)) band located at 766.0+/-0.4, 773.4+/-1.1, and 782.7+/-0.9 cm(-1), and assigned to spectroscopically free anions, ion pairs, and dimers, respectively. The solvation number of the lithium ion, which should be three in the limit of infinite dilution, decreases as the salt concentration increases as a result of the ionic pairing. However, the ionic pairing of LiBF4 in acrylonitrile is less than that previously observed in lithium trifluoromethanesulfonate (triflate) or lithium perchlorate.
引用
收藏
页码:781 / 797
页数:17
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