Structural and molecular recognition studies with acyclic anion receptors

被引：708

作者：

Gale, Philip A. ^{[1
]}

机构：

[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England

来源：

ACCOUNTS OF CHEMICAL RESEARCH | 2006年 / 39卷 / 07期

关键词：

D O I：

10.1021/ar040237q

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Acyclic molecules containing amides, ureas, and pyrrole groups have proven to be effective and selective anion-binding agents. In this Account, the structural chemistry of isophthalamide anion complexes, ortho-phenylenediamine based bis-ureas, and amidopyrroles, as well as anion-triggered deprotonation processes in neutral anion receptor systems, are discussed.

引用

页码：465 / 475

页数：11

共 41 条

[1]

Ashcroft F.M., 2000, Ion Channels and Disease

[2]

ASHNAGAR A, 1984, BIOCHIM BIOPHYS ACTA, V801, P351, DOI 10.1016/0304-4165(84)90138-7

[3] Anion-induced urea deprotonation [J].

Boiocchi, M ;

Del Boca, L ;

Esteban-Gómez, D ;

Fabbrizzi, L ;

Licchelli, M ;

Monzani, E .

CHEMISTRY-A EUROPEAN JOURNAL, 2005, 11 (10) :3097-3104

[4] Electrochemical measurement of switchable hydrogen bonding in an anthraquinone-based anion receptor [J].

Brooks, SJ ;

Birkin, PR ;

Gale, PA .

ELECTROCHEMISTRY COMMUNICATIONS, 2005, 7 (12) :1351-1356

[5] ortho-Phenylenediamine bis-urea-carboxylate:: a new reliable supramolecular synthon [J].

Brooks, SJ ;

Gale, PA ;

Light, ME .

CRYSTENGCOMM, 2005, 7 :586-591

[6] 'Twisted' isophthalamide analogues [J].

Brooks, SJ ;

Evans, LS ;

Gale, PA ;

Hursthouse, MB ;

Light, ME .

CHEMICAL COMMUNICATIONS, 2005, (06) :734-736

[7] Carboxylate complexation by a family of easy-to-make ortho-phenylenediamine based bis-ureas:: studies in solution and the solid state [J].

Brooks, SJ ;

Edwards, PR ;

Gale, PA ;

Light, ME .

NEW JOURNAL OF CHEMISTRY, 2006, 30 (01) :65-70

[8] Carboxylate complexation by 1,1′-(1,2-phenylene)bis(3-phenylurea) in solution and the solid state [J].

Brooks, SJ ;

Gale, PA ;

Light, ME .

CHEMICAL COMMUNICATIONS, 2005, (37) :4696-4698

[9] CYTOKININ ACTIVITY OF SOME SUBSTITUTED AREAS AND THIOUREAS [J].

BRUCE, MI ;

ZWAR, JA .

PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1966, 165 (999) :245-+

[10] 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

← 1 2 3 4 5 →