Pasgreta Ewa, Puchta Ralph, Galle Michael, van Eikema Hommes Nico, Zahl Achim, van Eldik Rudi
Institute for Inorganic Chemistry, University of Erlangen-Nürnberg, 91058 Erlangen, Germany.
Chemphyschem. 2007 Jun 25;8(9):1315-20. doi: 10.1002/cphc.200600624.
Solutions of LiClO(4) in solvent mixtures consisting of dimethylsulfoxide (DMSO) and water, or DMSO and gamma-butyrolactone, were studied by (7)Li NMR spectroscopy (for complexation by cryptands in gamma-butyrolactone as a solvent, see: E. Pasgreta, R. Puchta, M. Galle, N. J. R. van Eikema Hommes, A. Zahl, R. van Eldik, J. Incl. Phen., 2007, 58, 81-88). Chemical shifts indicate that the Li(+) ion is coordinated by four DMSO molecules. In the binary solvent mixture of water and DMSO, no selective solvation is detected, thus indicating that on increasing the water content of the solvent mixture, DMSO is gradually displaced by water in the coordination sphere of Li(+). The ligand-exchange mechanism of Li(+) ions solvated by DMSO and water/DMSO mixtures was studied using DFT calculations. Ligand exchange on Li(DMSO)(4) was found to follow a limiting associative (A) mechanism. The displacement of coordinated H(2)O by DMSO in Li(H(2)O)(4) follows an associative interchange mechanism. The suggested mechanisms are discussed in reference to available experimental and theoretical data.
通过⁷Li核磁共振光谱研究了高氯酸锂在由二甲基亚砜(DMSO)和水或DMSO和γ-丁内酯组成的溶剂混合物中的溶液(关于γ-丁内酯作为溶剂时穴状配体的络合情况,见:E. Pasgreta,R. Puchta,M. Galle,N. J. R. van Eikema Hommes,A. Zahl,R. van Eldik,J. Incl. Phen.,2007,58,81 - 88)。化学位移表明Li⁺离子由四个DMSO分子配位。在水和DMSO的二元溶剂混合物中,未检测到选择性溶剂化,因此表明随着溶剂混合物中水含量的增加,DMSO在Li⁺的配位球中逐渐被水取代。使用密度泛函理论计算研究了由DMSO以及水/DMSO混合物溶剂化的Li⁺离子的配体交换机制。发现[Li(DMSO)₄]⁺上的配体交换遵循极限缔合(A)机制。在[Li(H₂O)₄]⁺中,DMSO取代配位的H₂O遵循缔合交换机制。参考现有的实验和理论数据对所提出的机制进行了讨论。