It is found that the triplet-triplet energy transfer (ET) reaction between triplet benzophenone ('BP\*) and l-naphthol (ROH) is competitive with the hydrogen atom abstraction (HA) reaction. The rate constant of ET is enhanced with an increase of solvent polarity while that of HA is reduced. A possib
Solvent dependence of interactions between triplet benzophenone and N,N-dimethylaminonaphthalene studied by laser flash photolysis
โ Scribed by Minoru Yamaji; Tatsuya Kiyota; Haruo Shizuka
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 514 KB
- Volume
- 226
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
It is found by nanosecond laser flash photolysis at 355 nm that triplet energy transfer from triplet benzophenone ('BP*) to N,Ndimethylaminonaphthalene (RNMe,) occurs to yield triplet RNMe, with an efftciency of 0.58 in acetonitrile ( ACN) whereas electron transfer from RNMea to 3BP* takes place to produce the benzophenone anion and RNMe, cation radicals with an efftciency of 1 .O in ACN: Ha0 (4: 1 v/v) at 295 K. A possible mechanism for electron transfer of the BP-RNMe, system in the presence of Ha0 is discussed.
๐ SIMILAR VOLUMES
Laboratory-synthesized meso-tetrakis(rl-carboxyphenyl)porphyrin (TPPC) binds with the water-soluble polymer poly( N-vinyl-2-pyrrolidone) (PVP) at pH 10, with a binding constant K=3.7~ 10" M-'. The fluorescence lifetime of TPPC becomes biexponential in the polymer matrix. Generation of a radical-ion