Kang, Jongmin In, Sungjae Cho, Seung Joo 2024-01-21T00:34:43Z 2024-01-21T00:34:43Z 2021-09-05 2007-08 1061-0278 https://pubs.kist.re.kr/handle/201004/134231 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. English TAYLOR & FRANCIS LTD RHENIUM(I) BIPYRIDYL LIQUID-CRYSTALLINITY BINDING-PROPERTIES RECOGNITION CLIPS COORDINATION CHEMISTRY RUTHENIUM(II) COBALTOCENIUM POLYROTAXANE Anion receptors with glycoluril molecular scaffold Article 10.1080/10610270701358491 1 SUPRAMOLECULAR CHEMISTRY, v.19, no.4-5, pp.243 - 249 SUPRAMOLECULAR CHEMISTRY 19 4-5 243 249 scie scopus 000250011300004 2-s2.0-34547996927 Chemistry, Multidisciplinary Chemistry Article RHENIUM(I) BIPYRIDYL LIQUID-CRYSTALLINITY BINDING-PROPERTIES RECOGNITION CLIPS COORDINATION CHEMISTRY RUTHENIUM(II) COBALTOCENIUM POLYROTAXANE glycoluril anion receptor synthetic receptor molecular scaffold