Home / Publications / Acid-controlled photoreactivity of 9-(4’-azidophenyl)acridine

Acid-controlled photoreactivity of 9-(4’-azidophenyl)acridine

Mikhail Fedorovich Budyka 1
Mikhail Fedorovich Budyka
, 
Natalya Vladimirovna Biktimirova 1
Natalya Vladimirovna Biktimirova
, 
Tatyana Nikolaevna Gavrishova 1
Tatyana Nikolaevna Gavrishova
, 
Olga Dmitrievna Laukhina 1
Olga Dmitrievna Laukhina
10.1070/MC2004v014n03ABEH001868
Published 2004-05-27
Communication , Volume 14, Issue 3, 119-121
8
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Budyka M. F. et al. Acid-controlled photoreactivity of 9-(4’-azidophenyl)acridine // Mendeleev Communications. 2004. Vol. 14. No. 3. pp. 119-121.
GOST all authors (up to 50) Copy
Budyka M. F., Biktimirova N. V., Gavrishova T. N., Laukhina O. D. Acid-controlled photoreactivity of 9-(4’-azidophenyl)acridine // Mendeleev Communications. 2004. Vol. 14. No. 3. pp. 119-121.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1070/MC2004v014n03ABEH001868
UR - https://mendcomm.colab.ws/publications/10.1070/MC2004v014n03ABEH001868
TI - Acid-controlled photoreactivity of 9-(4’-azidophenyl)acridine
T2 - Mendeleev Communications
AU - Budyka, Mikhail Fedorovich
AU - Biktimirova, Natalya Vladimirovna
AU - Gavrishova, Tatyana Nikolaevna
AU - Laukhina, Olga Dmitrievna
PY - 2004
DA - 2004/05/27
PB - Mendeleev Communications
SP - 119-121
IS - 3
VL - 14
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2004_Budyka,
author = {Mikhail Fedorovich Budyka and Natalya Vladimirovna Biktimirova and Tatyana Nikolaevna Gavrishova and Olga Dmitrievna Laukhina},
title = {Acid-controlled photoreactivity of 9-(4’-azidophenyl)acridine},
journal = {Mendeleev Communications},
year = {2004},
volume = {14},
publisher = {Mendeleev Communications},
month = {May},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2004v014n03ABEH001868},
number = {3},
pages = {119--121},
doi = {10.1070/MC2004v014n03ABEH001868}
}
MLA
Cite this
MLA Copy
Budyka, Mikhail Fedorovich, et al. “Acid-controlled photoreactivity of 9-(4’-azidophenyl)acridine.” Mendeleev Communications, vol. 14, no. 3, May. 2004, pp. 119-121. https://mendcomm.colab.ws/publications/10.1070/MC2004v014n03ABEH001868.

Abstract

The possibility to control the photodissociation quantum yield of aromatic azide within two orders of magnitude by varying acid concentration is demonstrated using 9-(4’-azidophenyl)acridine as an example.

References

1.
10.1070/MC2004v014n03ABEH001868_bib1_1
Azides and Nitrenes, 1984
2.
10.1070/MC2004v014n03ABEH001868_bib1_2
Budyka
Zh. Fiz. Khim., 2000
3.
10.1070/MC2004v014n03ABEH001868_bib2
Budyka
Khim. Geterotsikl. Soedin., 1997
4.
Thermal and Photochemical Reactions of 10-Methyl-9-phenylacridinium Chloride in Alcohols
Zhou B., Kano K., Hashimoto S.
Bulletin of the Chemical Society of Japan, 1988
5.
Quenching of the excited singlet state of acridine and 10-methylacridinium cation by thio-organic compounds in aqueous solution
Pedzinski T., Marciniak B., Hug G.L.
Journal of Photochemistry and Photobiology A: Chemistry, 2002
6.
Theoretical investigation of azido group dissociation in aromatic azides
Budyka M.F., Zyubina T.S.
Journal of Molecular Structure THEOCHEM, 1997
7.
10.1070/MC2004v014n03ABEH001868_bib5_1
Stewart
J. Comput. Chem., 1989
8.
Optimization of parameters for semiempirical methods II. Applications
Stewart J.J.
Journal of Computational Chemistry, 1989
9.
Excited State Electron and Proton Transfers
Kosower E.M., Huppert D.
Annual Review of Physical Chemistry, 1986