Formation of triplets of aromatic hydrocarbons on quenching of excited singlet states by nitroxyl radicals
โ Scribed by V.A. Kuzmin; A.S. Tatikolov
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- English
- Weight
- 237 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
Quenching of aromatic excited singlet states (9,10-dimethyl anthracene, 9,10-diphenyl anthracene and perylene) by nitroxyl radical was studied by flash photolysis and fluorimetrically. It is established that the dominant quenching mechanism is enhanced intersystem crossing in the collision complex with the radical, but enhanced internal conversion also ccntributes to a significant extent (particularly in the case of 9.1~diphenyl anthracene and peryiene).
๐ SIMILAR VOLUMES
The mechanism of fluorescence quenching of anthracene by dimethylmercury, tetramethyllead end tetramethyltin has been examined by fluorescence and flash photolysis measurements. The increased rates OF SI -T, and TI -S6 Intersystem-crossings induced by the heavy-atom molecules are discussed
The dynamic nature of the quenching of the fluorescence of 1,4\_amino-and hydroxy-substituted 9, IO-anthraquinone, with benzene, alkylbenzenes and other aryl hydrocarbons as quenchers, indicates formation of exciplexes, where charge transfer (CT) occurs from the S, (quencher) to the S, (fluoropliore
Evidence rs presented that the excited singlet and triplet states of aromatic hydrocarbons are oxidised by methyi viologen (hlV2>. Rate constants for electron transfer from triplet naphthalene, anthracene, phenanthrene and fluoranthene are close to diffusion-controlled whereas those for triplet l-cy