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
相关论文
共 42 条
[1]   Binding of neutral substrates by calix[4]pyrroles [J].
Allen, WE ;
Gale, PA ;
Brown, CT ;
Lynch, VM ;
Sessler, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (49) :12471-12472
[2]   Reactivity of ions and ion pairs in the nucleophilic substitution reaction on methyl p-nitrobenzenesulfonate [J].
Alunni, S ;
Pero, A ;
Reichenbach, G .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1998, (08) :1747-1750
[3]  
Anzenbacher P, 2000, J AM CHEM SOC, V122, P10268
[4]  
Baeyer A., 1886, Ber. Dtsch. Chem. Ges, V19, P2184, DOI [10.1002/cber.188601902121, DOI 10.1002/CBER.188601902121]
[5]   Ionic liquid-calix[4]pyrrole complexes: pyridinium inclusion in the calixpyrrole cup [J].
Bates, Gareth W. ;
Gale, Philip A. ;
Light, Mark E. .
CRYSTENGCOMM, 2006, 8 (04) :300-302
[6]   Organic salt inclusion:: the first crystal structures of anion complexes of N-confused calix[4] pyrrole [J].
Bates, Gareth W. ;
Kostermans, Maarten ;
Dehaen, Wim ;
Gale, Philip A. ;
Light, Mark E. .
CRYSTENGCOMM, 2006, 8 (06) :444-447
[7]   Theoretical study of anion binding to calix[4]pyrrole:: the effects of solvent, fluorine substitution, cosolute, and water traces [J].
Blas, JR ;
Márquez, M ;
Sessler, JL ;
Luque, FJ ;
Orozco, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (43) :12796-12805
[8]   The complexation of halide ions by a calix[6]pyrrole [J].
Cafeo, G ;
Kohnke, FH ;
La Torre, GL ;
White, AJP ;
Williams, DJ .
CHEMICAL COMMUNICATIONS, 2000, (13) :1207-1208
[9]   Solution and solid-state studies of 3,4-dichloro-2,5-diamidopyrroles: formation of an unusual anionic narcissistic dimer [J].
Camiolo, S ;
Gale, PA ;
Hursthouse, MB ;
Light, ME ;
Shi, AJ .
CHEMICAL COMMUNICATIONS, 2002, (07) :758-759
[10]   Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonation [J].
Camiolo, S ;
Gale, PA ;
Hursthouse, MB ;
Light, ME .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2003, 1 (04) :741-744