Fluorescent sensors for molecules. Guest-responsive monomer and excimer fluorescence of 6A,6B-; 6A,6C-; 6A,6D-; and 6A,6E-bis(2-naphthylsulfonyl)-gamma-cyclodextrins

被引:31
作者
Hamada, F
Minato, S
Osa, T
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
10.1246/bcsj.70.1339
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Flexible hosts, 6A,6B-; 6A,6C-; 6A,6D-; and 6A,6E-bis(2-naphthylsulfonyl)-gamma-cyclodextrins (gamma-1, gamma-2, gamma-3, and gamma-4, respectively) were used as fluorescent sensors with which a variety of organic compounds were detected by naphthalene excimer and monomer emissions. In a 10 vol% ethylene glycol aqueous solution, gamma-1 exhibits almost pure monomer fluorescence while gamma-2, gamma-3, and gamma-4 exhibit both monomer and excimer emissions. The intensities of the emissions changed upon addition of guest species, particularly in the case of gamma-2 and gamma-3, and the guest-induced intensity variations were used as sensitivity factors of the sensors. When (-)-borneol (5), cyclohexanol (6), cyclododecanol (7), and 1-adamantanecarboxylic acid (8) were added to each host solution, gamma-2, gamma-3, and gamma-4 increased the excimer emission intensity but decreased the monomer one, the absolute intensity variations being 6 < 5 approximate to 8 < 7. When geraniol (9), nerol (10), and (-)-menthol (11) were added, the hosts decreased intensities in both monomer and excimer emissions for 9 and 10 while their emission variations for 11 were similar to those of 5. For steroids such as cholic acid (12), deoxycholic acid (13), chenodeoxycholic acid (14), and ursodeoxycholic acid (15), gamma-4 showed depression in the excimer emission and enhancement in the monomer one while gamma-2 and gamma-3 showed complicated features in which the excimer emission was enhanced with the order of 15 < 14 < 13 approximate to 12 but the monomer one was depressed or enhanced depending on the hosts. All these data demonstrate that the hosts can be used as sensors for molecular recognition.
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页码:1339 / 1346
页数:8
相关论文
共 25 条
[1]  
Bender M.L., 1977, CYCLODEXTRIN CHEM
[2]  
CZARNIK AW, 1991, FRONTIERS SUPRAMOLEC, P109
[3]   Fluorescent amino acids as reporter systems in peptido-cyclodextrin inclusion compounds [J].
Eddaoudi, M ;
ParrotLopez, H ;
deLamotte, SP ;
Ficheux, D ;
Prognon, P ;
Coleman, AW .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1996, (08) :1711-1715
[4]   MOLECULAR-RECOGNITION AND SENSORY SYSTEM OF GAMMA-CYCLODEXTRIN CAPPED BY SODIUM ANTHRANILATE [J].
HAMADA, F ;
ISHIKAWA, K ;
TAMURA, I ;
UENO, A .
ANALYTICAL SCIENCES, 1995, 11 (06) :935-939
[5]   HOST-GUEST SENSORY SYSTEM OF SODIUM ANTHRANILATE-MODIFIED BETA-CYCLODEXTRIN - MOLECULAR RECOGNITION PROPERTIES [J].
HAMADA, F ;
KONDO, Y ;
ISHIKAWA, K ;
ITO, H ;
SUZUKI, I ;
OSA, T ;
UENO, A .
JOURNAL OF INCLUSION PHENOMENA AND MOLECULAR RECOGNITION IN CHEMISTRY, 1994, 17 (03) :267-275
[6]  
HAMADA F, 1993, J INCLUS PHENOM MOL, V15, P273
[7]  
HAMADA F, 1995, J INCLUSION PHENOM, V20, P43
[8]  
Harada N., 1982, CIRCULAR DICHROIC SP
[9]   INCLUSION COMPLEX-FORMATION OF GAMMA-CYCLODEXTRIN - ONE HOST-2 GUEST COMPLEXATION WITH WATER-SOLUBLE DYES IN GROUND-STATE [J].
HIRAI, H ;
TOSHIMA, N ;
UENOYAMA, S .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1985, 58 (04) :1156-1164
[10]   Synthesis and characterization of dicyanoanthracene-tethered beta-cyclodextrins [J].
Hubbard, BK ;
Beilstein, LA ;
Heath, CE ;
Abelt, CJ .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1996, (05) :1005-1009