A novel fluorescent 2,2′-bipyridine derivative prepared by coupling to a fluorescent aminophenazine-fluorescence properties and response toward various cations

被引:29
作者
Choi, CS [1 ]
Mutai, T [1 ]
Arita, S [1 ]
Araki, K [1 ]
机构
[1] Univ Tokyo, Inst Ind Sci, Minato Ku, Tokyo 1068558, Japan
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2 | 2000年 / 02期
关键词
D O I
10.1039/a908122d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
2,2'-Bipyridine (bpy), a non-fluorescent but good metal-chelating unit, and 2-aminophenazine (2-aphz), a good fluorescent unit, are integrated to give 7-aminodipyrido[3,2-a:2',3'-c]phenazine (7-amino-dppz) 1. Compound 1 exhibits an efficient fluorescence at 517 nm (Phi = 0.24, dichloromethane), which is similar to the parent 2-aphz. It is suggested that the orbitals involved in the photoexcitation process are mostly localized on the phenazine unit. However, addition of divalent metal ions such as Mg2+, Ca2+ and Cu2+ causes a noticeable fluorescence response, which is attributed to coordination of these cations to the bpy chelation site of 1. This behaviour indicates that sufficient electronic communication exists between the bpy chelation site and the phenazine fluorophore. 7-(4-tert-Butylbenzoylamino)dppz 2 also showed a fluorescence response towards divalent metal ions.
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页码:243 / 247
页数:5
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