Abstract
Photophysical and photochemical properties of phenothiazine and N-alkylphenothiazines (alkyl ≡ methyl, ethyl, isobutyl, phenyl, benzyl) in acetonitrile were studied by means of nanosecond laser flash photolysis. Transient absorption measurements showed that the excited triplet state, radical cation, neutral radical, dimeric radical cation and dimeric dication were formed during the photolysis. The kinetics of the formation and conversion of the transient species was investigated. The deprotonation of the phenothiazine radical cation (PTH-+ ) to give the neutral radical PT+ was prevented by the presence of tetracyanoethylene (TCNE). The mechanism of the interaction of phenothiazines and TCNE is discussed.
Original language | English |
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Pages (from-to) | 27-31 |
Number of pages | 5 |
Journal | Journal of Photochemistry and Photobiology A: Chemistry |
Volume | 93 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 4 1996 |
Externally published | Yes |
ASJC Scopus Subject Areas
- General Chemistry
- General Chemical Engineering
- General Physics and Astronomy
Keywords
- Excited triplet state
- Laser flash photolysis
- Phenothiazine derivatives
- Radical cation
- TCNE