1996 年 54 巻 4 号 p. 311-322
Artificial ribofuranoside receptors represent the molecular design and the synthetic strategy for our multi-functional artificial receptors. The design of the polypyridine-macrocyclic ribofuranoside receptors was based on the multipoint hydrogen bond complementarity between the receptors and methyl β- (D) -ribofuranoside. The binding affinity of the receptors for the ribofuranoside in CDCl3 was very high (up to Ka = 5.2 × 103M-1), so that even native ribose was extracted by them into such nonpolar solvents. Selective extraction of ribose by the receptors was observed. The selectivity is governed by the OH direction and the whole size of the sugars as well as their shapes. Furthermore, fluorescence emission of the receptors was largely enhanced in the presence of methyl β- (D) -ribofuranoside or ribose.