UV-visible, 1H and 13C NMR spectroscopic studies on the interaction between protons or alkaline earth metal ions and the benzoate ion in acetonitrile

被引:14
作者
Hojo, Masashi [1 ]
Ueda, Tadaharu [1 ]
Ike, Michitaka [1 ]
Kobayashi, Masato [2 ]
Nakai, Hiromi [2 ]
机构
[1] Kochi Univ, Dept Chem, Fac Sci, Akebono, Kochi 7808520, Japan
[2] Waseda Univ, Dept Chem & Biochem, Sch Adv Sci & Engn, Tokyo 1698555, Japan
基金
日本学术振兴会;
关键词
Protonated benzoic acid; Hofmeister series; Magnesium benzoate; Density functional theory; TRITYL CHLORIDES; CHEMICAL-SHIFTS; CARBOCATIONS; ACIDS; COMPLEXES; CATIONS; LITHIUM; RATES; PERCHLORATES; ELUCIDATION;
D O I
10.1016/j.molliq.2008.06.004
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
The interaction between protons (H+) or alkaline earth metal ions (Mg2+, Ba2+) and the benzoate ion has been examined in acetonitrile by means of UV-visible, H-1 and C-13 NMR spectroscopy. The assignments of C-13 NMR spectra for the benzoate ion (L-), benzoic acid (HL), and the protonated benzoic acid (H2L+) in acetonitrile were properly performed by means of theoretical calculations, including the influence of the acetonitrile solvent by using the self-consistent isodensity polarized continuum model and the polarized continuum model. It is demonstrated that "strong" interactions of alkaline earth metal ions (M2+=Mg2+, Ba2+) with the benzoate ion (L-) lead to the formation of mono-charged species, ML+, as well as non-charged species, ML2, in acetonitrile solution: the strong ability in coordination for alkaline earth metal ions is verified. (C) 2008 Elsevier B.V. All rights reserved.
引用
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页码:152 / 157
页数:6
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