Calix[4]pyrrole as a chloride anion receptor: Solvent and countercation effects

被引:316
作者
Sessler, Jonathan L.
Gross, Dustin E.
Cho, Won-Seob
Lynch, Vincent M.
Schmidtchen, Franz P.
Bates, Gareth W.
Light, Mark E.
Gale, Philip A.
机构
[1] Univ Texas, Dept Chem & Biochem, Inst Mol & Cellular Biol, Austin, TX 78712 USA
[2] Tech Univ Munich, Dept Chem, D-85747 Garching, Germany
[3] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1021/ja064012h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interaction of calixpyrrole with several chloride salts has been studied in the solid state by X-ray crystallography as well as in solution by isothermal titration calorimetry (ITC) and H-1 NMR spectroscopic titrations. The titration results in dimethylsulfoxide, acetonitrile, nitromethane, 1,2-dichloroethane, and dichloromethane, carried out using various chloride salts, specifically tetraethylammonium (TEA), tetrapropylammonium (TPA), tetrabutylammonium (TBA), tetraethylphosphonium (TEP), tetrabutylphosphonium (TBP), and tetraphenylphosphonium (TPhP), showed no dependence on method of measurement. The resulting affinity constants (K-a), on the other hand, were found to be highly dependent on the choice of solvent with K-a's ranging from 10(2)-10(5) M-1 being recorded in the test solvents used for this study. In dichloromethane, a strong dependence on the countercation was also seen, with the Ka's for the interaction with chloride ranging from 10(2)-10(4) M-1. In the case of TPA, TBA, and TBP, the ITC data could not be fit to a 1:1 binding profile.
引用
收藏
页码:12281 / 12288
页数:8
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