Time-resolved fluorescence spectroscopy for illuminating complex systems

被引:49
作者
Bright, FV [1 ]
Munson, CA [1 ]
机构
[1] SUNY Buffalo, Dept Chem, Buffalo, NY 14260 USA
关键词
time-resolved; fluorescence spectroscopy; photophysics;
D O I
10.1016/S0003-2670(03)00723-2
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Over the years, the emissive characteristics (spectral, temporal, and polarization) of fluorophores have been widely used to probe a wide variety of systems. Fluorescence lifetime and rotational reorientation time measurements, in particular, offer a means to elucidate key details about complex systems. Further, because fluorescence occurs on the nanosecond (10(-9) s) timescale, competing or perturbing kinetic processes like collisional quenching, solvent relaxation, energy transfer, and rotational reorientation can affect the fluorescence and hence be quantified. Thus, a carefully chosen and "placed" fluorophore can serve as an reporter on a wide range of nanosecond or faster events. This contribution is divided into three sections. The Theory section discusses time-resolved anisotropy and intensity decay kinetics (time and frequency domains), pump-probe spectroscopy, and up-conversion. The second section describes time-correlated single photon counting (TC-SPC) and multifrequency phase-modulation fluorescence instruments. The final section is divided into subsections on the use of time-resolved fluorescence: (1) to study solvation dynamics, biochemical systems, polymer photophysics, and organized media; (2) as a tool in the separation sciences, microscopy, and sensing; and (3) coupled with multiphoton excitation strategies. (C) 2003 Elsevier B.V All rights reserved.
引用
收藏
页码:71 / 104
页数:34
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