In a recent paper, Lessing and von Jena claim that certain results reported by Shank and Ippen are incorrect. This reply IS to point out that their claim is ill-founded and that the original results are correct.
Separation of rotational diffusion and level kinetics in transient absorption spectroscopy
β Scribed by H.E. Lessing; A. Von Jena
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 502 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Transient absorption spectroscopy on electronic levels of molecules in the liquid phase is governed by population kinetics as well as rotational diffusion. The goal of transient absorption experiments has been the true level kinetics free of rotation. hforeover, to extract the rotational relAy.uation time from transient photodichroism experiments the knowledge of true population kmetics is instrument& Three methods for separating rotationai and level kinetics are described theoretically, and one of them is performed experimentally using a repetitive picosecond spectrometer for the measurement of rotational behaviour of fluorcsccin 27 in solvents of different viscosity.
π SIMILAR VOLUMES
The rotational diffusion time constants of tetrachlorotetraiodotluorescein in a series of low viscosity, hydrogen bonding solvents have been determined by picosecond time-resolved fluorescence depolarisation spectroscopy. Steady state measurements of this dye and rhodamine 6G have been used to obtai
## Abstract We explain the transient absorption kinetics (E. Romero, I. H. M. van Stokkum, V. I. Novoderezhkin, J. P. Dekker, R. van Grondelle, __Biochemistry__ **2010**, __49__, 4300) measured for isolated reaction centers of photosystem II at 77 K upon excitation of the primary donor band (680 nm