INTRAMOLECULAR EXCIMER FORMATION AND MOLECULAR RECOGNITION OF MODIFIED CYCLODEXTRINS APPENDED BY 2 NAPHTHALENE RINGS

被引:20
作者
MINATO, S
OSA, T
MORITA, M
NAKAMURA, A
IKEDA, H
TODA, F
UENO, A
机构
[1] TOHOKU UNIV,INST PHARMACEUT,SENDAI,MIYAGI 980,JAPAN
[2] TOKYO INST TECHNOL,FAC BIOSCI & BIOTECHNOL,DEPT BIOENGN,MIDORI KU,YOKOHAMA,KANAGAWA 227,JAPAN
关键词
D O I
10.1111/j.1751-1097.1991.tb02061.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The intramolecular excimer formation of 6A,6B-, 6A,6C-, 6A,6D-, and 6A,6E-bis(2-naphthyl-sulfonyl)-gamma-cyclodextrins (1, 2, 3, and 4, respectively) and 6A,6B-, 6A,6C-, and 6A,6D-bis(2-naphthyl-sulfonyl)-beta-cyclodextrins (5, 6, and 7, respectively) has been studied in 10% ethylene glycol aqueous solution. The two naphthyl rings are co-included in the gamma-cyclodextrin cavities of 1-4, and marked excimer emission was observed for 2, 3, and 4. On the other hand, almost pure monomer emission was observed for 5, 6, and 7 due to inclusion of one of two naphthyl rings in the beta-cyclodextrin cavities. Compounds 2, 3, 6, and 7 showed remarkable guest-induced enhancement in the excimer emission, and this property was used for detecting several organic compounds with remarkable molecular recognition.
引用
收藏
页码:593 / 597
页数:5
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