Oligosaccharide binding to a boronic-acid-appended phenanthroline-Cu(I) complex which creates superstructural helicates and catenates

被引:20
作者
Yamamoto, M [1 ]
Takeuchi, M [1 ]
Shinkai, S [1 ]
机构
[1] Kyushu Univ, Grad Sch Engn, Dept Chem & Biochem, Fukuoka 8128581, Japan
关键词
superstructural helicates and catenates; helicity; oligosaccharide binding;
D O I
10.1016/S0040-4020(02)00786-X
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Compound 2 bearing two boronic acid moieties at two sides of a 1,10-phenanthroline moiety was synthesized. 2 forms a 1:2 complex with Cu(I) and four boronic acid groups are arranged in the peripheral positions around the central metal chelate. When a saccharide guest links two boronic acid groups in the different ligands, the resultant structure is classified into a helicate, whereas when a saccharide guest links two boronic acid groups in the same ligands, the resultant structure is classified into a catenate. Careful examination of the CD spectra of 2(2).Cu(I) complex with saccharides established that (i) the D-glucose complex gives the helicate with P-helicity, (ii) the maltose complex give the helicate with M-helicity, (iii) the maltopentaose and maltohexaose complexes give the catenate with P-helicity, and (iv) maltotriose and maltotetraose cannot provide the stable complex with 2(2).Cu(I). The results indicate that 22-Cu(I) can act as a versatile core to create various superstructures using a boronic acid-saccharide interaction. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:7251 / 7258
页数:8
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