Strapped and other topographically nonplanar calixpyrrole analogues. Improved anion receptors

被引:216
作者
Lee, Chang-Hee [1 ,2 ]
Miyaji, Hidekazu [1 ]
Yoon, Dae-Wi [1 ]
Sessler, Jonathan L. [1 ,2 ]
机构
[1] Kangwon Natl Univ, Dept Chem, Chunchon, South Korea
[2] Univ Texas, Inst Mol & Cellular Biol, Dept Chem & Biochem, Austin, TX 78712 USA
关键词
D O I
10.1039/b713183f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Calixpyrroles and related macrocycles are non-aromatic synthetic anion receptors that have attracted considerable attention in recent years. The unfunctionalized, parent calix[4] pyrrole system, also known as octamethylporphyrinogen, may be prepared in one step and in high yield from pyrrole and acetone, and is an effective anion receptor, showing a preference for fluoride, phosphate, carboxylate and chloride anions in organic media. Efforts to improve the anion binding affinity of calix[4] pyrrole and to modify its inherent selectivity have led to the synthesis of a variety of new, modified calixpyrroles. Among the most effective of these are derivatives that contain bridging "straps''. In this Feature Article, the preparation and properties of these and other topographically nonplanar calixpyrrole analogues are reviewed from the perspective of the anion recognition chemist.
引用
收藏
页码:24 / 34
页数:11
相关论文
共 48 条
[1]   DEMONSTRATION THAT CFTR IS A CHLORIDE CHANNEL BY ALTERATION OF ITS ANION SELECTIVITY [J].
ANDERSON, MP ;
GREGORY, RJ ;
THOMPSON, S ;
SOUZA, DW ;
PAUL, S ;
MULLIGAN, RC ;
SMITH, AE ;
WELSH, MJ .
SCIENCE, 1991, 253 (5016) :202-205
[2]   Calix[4]pyrroles containing deep cavities and fixed walls.: Synthesis, structural studies, and anion binding properties of the isomeric products derived from the condensation of p-hydroxyacetophenone and pyrrole [J].
Anzenbacher, P ;
Jursíková, K ;
Lynch, VM ;
Gale, PA ;
Sessler, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (47) :11020-11021
[3]  
BLANCHI A, 1997, SUPRAMOLECULAR CHEM
[4]   Engineering Deinococcus radiodurans for metal remediation in radioactive mixed waste environments [J].
Brim, H ;
McFarlan, SC ;
Fredrickson, JK ;
Minton, KW ;
Zhai, M ;
Wackett, LP ;
Daly, MJ .
NATURE BIOTECHNOLOGY, 2000, 18 (01) :85-90
[5]   First cryptand-like calixpyrrole: Synthesis, X-ray structure, and anion binding properties of a bicyclic[3,3,3]nonapyrrole [J].
Bucher, C ;
Zimmerman, RS ;
Lynch, V ;
Sessler, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (39) :9716-9717
[6]   Synthesis and X-ray structure of a three dimensional calixphyrin [J].
Bucher, C ;
Zimmerman, RS ;
Lynch, V ;
Sessler, JL .
CHEMICAL COMMUNICATIONS, 2003, (14) :1646-1647
[7]   ARGININE-MEDIATED RNA RECOGNITION - THE ARGININE FORK [J].
CALNAN, BJ ;
TIDOR, B ;
BIANCALANA, S ;
HUDSON, D ;
FRANKEL, AD .
SCIENCE, 1991, 252 (5009) :1167-1171
[8]   Fluoride recognition in 'super-extended cavity' calix[4]pyrroles [J].
Camiolo, S ;
Gale, PA .
CHEMICAL COMMUNICATIONS, 2000, (13) :1129-1130
[9]   ANION-BINDING SITES IN PROTEIN STRUCTURES [J].
CHAKRABARTI, P .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 234 (02) :463-482
[10]  
Colton R., 1965, The Chemistry of Rhenium and Technetium