Title of article
Time-resolved fluorescence spectroscopy for illuminating complex systems Review Article
Author/Authors
Frank V. Bright، نويسنده , , Chase A Munson، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2003
Pages
34
From page
71
To page
104
Abstract
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 (TCSPC) 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.
Keywords
Time-resolved , Fluorescence spectroscopy , Photophysics
Journal title
Analytica Chimica Acta
Serial Year
2003
Journal title
Analytica Chimica Acta
Record number
1030317
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