Relaxation processes of the singlet excited states of carotenoids containing a carbonyl group were investigated in relation to the molecular structure around the carbonyl group. The relative quantum yield of fluorescence from the allowed Sz state to the forbidden S, state follows the energy gap law
Quantitative analysis of the solvent effect on the relaxation processes of carotenoids showing dual emissive characteristics
โ Scribed by Mamoru Mimuro; Umpei Nagashima; Shin-ichi Nagaoka; Yoshinobu Nishimura; Shinichi Takaichi; Tetzuya Katoh; Iwao Yamazaki
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 354 KB
- Volume
- 191
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
The solvent effect on the fluorescence quantum yields of St (~1) and $2 (ยข~2) states of carotenoids containing a keto group is examined. The relative yields (~b2/~1) are expressed exponentially as a function of the reciprocal of the dielectric constants of several non-polar solvents. This relationship can be explained by the energy gap law of internal conversion from the second excited state of carotenoids. This leads to the first quantitative study of solvent effects on the relaxation process of carotenoids.
๐ SIMILAR VOLUMES
13C spin-lattice relaxation time measurements of buckminsterfullerene were performed in mixtures of protonated and deuterated toluene to determine the magnitude of the intermolecular contribution. Results show that a small but measurable contribution can be attributed to this mechanism. Inclusion of