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Formation of triplets of aromatic hydrocarbons on quenching of excited singlet states by nitroxyl radicals

โœ 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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โœฆ 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).


๐Ÿ“œ SIMILAR VOLUMES


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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