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Non-radiative deactivation via biradicaloid charge-transfer states in oxazine and thiazine dyes

✍ Scribed by Martin Vogel; Wolfgang Rettig; U. Fiedeldei; H. Baumgärtel


Book ID
103023603
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
446 KB
Volume
148
Category
Article
ISSN
0009-2614

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✦ Synopsis


Oxazine and thiazine dyes with dialkylamino (NR2) substituents exhibit a temperature/viscosity-dependent intramolecular fluorescence quenching which is absent if the substituents are NH2 and is especially fast for piperidino substituent groups. These results suggest that the driving force for this process is intramolecular donor-acceptor interaction (formation of a biradicaloid charge-transfer (BCT) state) which involves amino group twisting. Low-temperature studies reveal fluorescence risetimes and suggest there is an additional much faster relaxation process preceding BCT-state formation.


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