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Self-quenching in the stepwise photocyclization of 1,4-bis(diphenylamino)butane to 1,4-dicarbazolylbutane

Mikhail Fedorovich Budyka 1
Mikhail Fedorovich Budyka
Olga Dmitrievna Laukhina 1
Olga Dmitrievna Laukhina
Tatyana Nikolaevna Gavrishova 1
Tatyana Nikolaevna Gavrishova
Published 1998-04-28
CommunicationVolume 8, Issue 2, 59-60
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Budyka M. F., Laukhina O. D., Gavrishova T. N. Self-quenching in the stepwise photocyclization of 1,4-bis(diphenylamino)butane to 1,4-dicarbazolylbutane // Mendeleev Communications. 1998. Vol. 8. No. 2. pp. 59-60.
GOST all authors (up to 50) Copy
Budyka M. F., Laukhina O. D., Gavrishova T. N. Self-quenching in the stepwise photocyclization of 1,4-bis(diphenylamino)butane to 1,4-dicarbazolylbutane // Mendeleev Communications. 1998. Vol. 8. No. 2. pp. 59-60.
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TY - JOUR
DO - 10.1070/MC1998v008n02ABEH000901
UR - https://mendcomm.colab.ws/publications/10.1070/MC1998v008n02ABEH000901
TI - Self-quenching in the stepwise photocyclization of 1,4-bis(diphenylamino)butane to 1,4-dicarbazolylbutane
T2 - Mendeleev Communications
AU - Budyka, Mikhail Fedorovich
AU - Laukhina, Olga Dmitrievna
AU - Gavrishova, Tatyana Nikolaevna
PY - 1998
DA - 1998/04/28
PB - Mendeleev Communications
SP - 59-60
IS - 2
VL - 8
ER -
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@article{1998_Budyka,
author = {Mikhail Fedorovich Budyka and Olga Dmitrievna Laukhina and Tatyana Nikolaevna Gavrishova},
title = {Self-quenching in the stepwise photocyclization of 1,4-bis(diphenylamino)butane to 1,4-dicarbazolylbutane},
journal = {Mendeleev Communications},
year = {1998},
volume = {8},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1998v008n02ABEH000901},
number = {2},
pages = {59--60},
doi = {10.1070/MC1998v008n02ABEH000901}
}
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Budyka, Mikhail Fedorovich, et al. “Self-quenching in the stepwise photocyclization of 1,4-bis(diphenylamino)butane to 1,4-dicarbazolylbutane.” Mendeleev Communications, vol. 8, no. 2, Apr. 1998, pp. 59-60. https://mendcomm.colab.ws/publications/10.1070/MC1998v008n02ABEH000901.

Abstract

The quantum yields of stepwise cyclization of the first and second diphenylamino groups in 1,4-bis(diphenylamino)butane are 0.3 and 0.02, respectively, which indicates quenching of the excited diphenylamino group by a carbazole unit in the asymmetric semicyclized compound.

References

1.
Reaction patterns and kinetics of the photoconversion of N-methyldiphenylamine to N-methylcarbazole
Foerster E.W., Grellmann K.H., Linschitz H.
Journal of the American Chemical Society, 1973
2.
Photochemical formation of dihydrocarbazoles from diphenylamines and their thermal rearrangement and disproportionation reactions
3.
Kinetics and mechanism of the photocyclization of diphenylamines. I. Photochemical primary processes of diphenylamines
Tanaka I., Shizuka H., Takayama Y., Morita T.
Journal of the American Chemical Society, 1970
4.
Effects of hydrogen bonding on the photocyclization of diphenylamines
Amano K., Hinohara T., Hoshino M.
Journal of Photochemistry and Photobiology A: Chemistry, 1991
6.
Intramolecular excimer formation in carbazole double molecules
7.
Intramolecular Excimers with α, ω-Diarylalkanes
Zachariasse K., Kühnle W.
Zeitschrift fur Physikalische Chemie, 1976
8.
Fluorescent excimer formation by α,ω-diaminoalkanes and related compounds
Beecroft R.A., Davidson R.S., Whelan T.D.
Journal of the Chemical Society Perkin Transactions 2, 1985
9.
Intramolecular excimer formation in bichromophoric molecules linked by a short flexible chain
De Schryver F.C., Collart P., Vandendriessche J., Goedeweeck R., Swinnen A.M., Van der Auweraer M.
Accounts of Chemical Research, 1987
11.
10.1070/MC1998v008n02ABEH000901_bib11
Budyka
Izv. Akad. Nauk, Ser. Khim., 1995
12.
Through-space and through-bond effects on exciton interactions in rigidly linked dinaphthyl molecules
Scholes G.D., Ghiggino K.P., Oliver A.M., Paddon-Row M.N.
Journal of the American Chemical Society, 1993
15.
Intramolecular triplet energy transfer. 3. A carbazole-naphthalene system having short chain length methylene spacer units
Haggquist G.W., Katayama H., Tsuchida A., Ito S., Yamamoto M.
The Journal of Physical Chemistry, 1993