Competition Between Energy Transfer Quenching and Chelation Enhanced Fluorescence in a Cu (II) Coordinated Conjugated Polymer System

被引:13
作者
Fan, Li-Juan [1 ,2 ]
Martin, Justin J. [2 ]
Jones, Wayne E., Jr. [2 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat, Key Lab Organ Synth Jiangsu Prov, Suzhou 215123, Peoples R China
[2] SUNY Binghamton, Dept Chem, Binghamton, NY 13902 USA
关键词
Conjugated polymer; Fluorescent chemosensor; Chelation enhanced fluorescence; Energy transfer quenching; Dexter (double-electron exchange) energy transfer; PHOTOINDUCED ELECTRON-TRANSFER; MOLECULAR WIRE APPROACH; TRANSFER MECHANISMS; TRANSITION-METALS; CHEMICAL SENSORS; CHEMOSENSORS; SWITCHES; LUMINESCENCE; MIGRATION;
D O I
10.1007/s10895-008-0444-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An investigation of the mechanism of the fluorescence quenching by Cu(2+) for a conjugated polymer system initially designed as a fluorescence "turn-on" chemosensor based on chelation enhanced fluorescence (CHEF) is described in this paper. Unlike all other metal cations tested, the polymer/Cu(2+) hybrid system with a 1:1 ratio between the receptor and Cu(2+) has only weak fluorescence with lambda(max) = 490 nm and a quantum yield of 0.004 in THF at room temperature. In solvent glasses at 77 K the fluorescence remained quenched suggesting that the quenching mechanism was due to energy transfer between the Cu(2+) and the conjugated polymer backbone. The energy transfer quenching competes effectively with the electron transfer involved in the CHEF resulting in a more selective chemosensory system.
引用
收藏
页码:555 / 559
页数:5
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