Anion receptors with glycoluril molecular scaffold

Authors
Kang, JongminIn, SungjaeCho, Seung Joo
Issue Date
2007-08
Publisher
TAYLOR & FRANCIS LTD
Citation
SUPRAMOLECULAR CHEMISTRY, v.19, no.4-5, pp.243 - 249
Abstract
For a synthetic receptor with an amide group, the amide groups are arranged through a space in a rigid and convergent manner. This has been achieved by incorporating amide groups into various molecular scaffolds. The geometry of diphenylglycoluril allows the synthesis of concave molecular structures. In addition, the rigidity of the molecule provides a solid molecular scaffold to arrange suitable binding moieties such as hydrogen bonds. We have developed various anion receptors based on diphenylglycoluril. The association of these receptors with various anions reflects the shape, size and basicity of the anions.
Keywords
RHENIUM(I) BIPYRIDYL; LIQUID-CRYSTALLINITY; BINDING-PROPERTIES; RECOGNITION; CLIPS; COORDINATION; CHEMISTRY; RUTHENIUM(II); COBALTOCENIUM; POLYROTAXANE; RHENIUM(I) BIPYRIDYL; LIQUID-CRYSTALLINITY; BINDING-PROPERTIES; RECOGNITION; CLIPS; COORDINATION; CHEMISTRY; RUTHENIUM(II); COBALTOCENIUM; POLYROTAXANE; glycoluril; anion receptor; synthetic receptor; molecular scaffold
ISSN
1061-0278
URI
https://pubs.kist.re.kr/handle/201004/134231
DOI
10.1080/10610270701358491
Appears in Collections:
KIST Article > 2007
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