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Electronic relaxation in aza derivatives of 1,2-benzanthracene and their protonated forms. A comparative study of the quantum yield of triplet-state formation

✍ Scribed by Andrzej Mordzinski; Stanisław J. Komorowski


Publisher
Elsevier Science
Year
1985
Tongue
English
Weight
526 KB
Volume
114
Category
Article
ISSN
0009-2614

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✦ Synopsis


Sl+

SO internal conversion (Jqd and S1 -+ T1 (JqSC) intersystem crossing rate constants were determined and compared in the group of mono-and di-aza derivatives of 1 ,Zbcnzanthracene.

Quantum y~clds of triplet formation (Uqsc) were obtained from puked photoacoustic measurements. The extremely fast k1SC = 4 X 10" s-l was found for 1 ,a-benzphenazinc in aprotic solvents. kIc of free bases and monoprotonated spenes are two orders of magnitude greater than that of the parent hydrocarbon.