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 (10-9s) 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.
| Original language | English |
|---|---|
| Pages (from-to) | 71-104 |
| Number of pages | 34 |
| Journal | Analytica Chimica Acta |
| Volume | 500 |
| Issue number | 1-2 |
| DOIs | |
| State | Published - Dec 19 2003 |
Keywords
- Fluorescence spectroscopy
- Photophysics
- Time-resolved
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