Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5400522 | Journal of Luminescence | 2014 | 6 Pages |
Abstract
The synthesis, structure and photoluminescence of a group of substituted 2-pyrazolylquinolines, including a spin-labelled derivative, are described. A comparative study of photoluminescence from the synthesized compounds demonstrates that introduction of a nitronyl nitroxide radical group results not only in the expected reduction in photoluminescence from the pyrazolylquinoline moiety, but also gives rise to a new red photoluminescence band (maximum at 692Â nm in acetonitrile) from the radical fragment.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Evgeny V. Tretyakov, Victor F. Plyusnin, Anastasiya O. Suvorova, Stanislav V. Larionov, Sergey A. Popov, Olga V. Antonova, Ekaterina M. Zueva, Dmitry V. Stass, Artem S. Bogomyakov, Galina V. Romanenko, Victor I. Ovcharenko,