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Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene

Igor Ivanovich Barabanov 1
Igor Ivanovich Barabanov
Alexander Valer'evich Polukhin 1
Alexander Valer'evich Polukhin
Valerii Vladimirovich Korolev 1, 2
Valerii Vladimirovich Korolev
Leonid Vasil'evich Kuibida 1, 2
Leonid Vasil'evich Kuibida
Andrey Alekseevich Nefedov 2, 3
Andrey Alekseevich Nefedov
Published 2015-07-08
CommunicationVolume 25, Issue 4, 260-261
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Barabanov I. I. et al. Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene // Mendeleev Communications. 2015. Vol. 25. No. 4. pp. 260-261.
GOST all authors (up to 50) Copy
Barabanov I. I., Polukhin A. V., Korolev V. V., Kuibida L. V., Nefedov A. A. Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene // Mendeleev Communications. 2015. Vol. 25. No. 4. pp. 260-261.
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TY - JOUR
DO - 10.1016/j.mencom.2015.07.008
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.008
TI - Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene
T2 - Mendeleev Communications
AU - Barabanov, Igor Ivanovich
AU - Polukhin, Alexander Valer'evich
AU - Korolev, Valerii Vladimirovich
AU - Kuibida, Leonid Vasil'evich
AU - Nefedov, Andrey Alekseevich
PY - 2015
DA - 2015/07/08
PB - Mendeleev Communications
SP - 260-261
IS - 4
VL - 25
ER -
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@article{2015_Barabanov,
author = {Igor Ivanovich Barabanov and Alexander Valer'evich Polukhin and Valerii Vladimirovich Korolev and Leonid Vasil'evich Kuibida and Andrey Alekseevich Nefedov},
title = {Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.008},
number = {4},
pages = {260--261},
doi = {10.1016/j.mencom.2015.07.008}
}
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Barabanov, Igor Ivanovich, et al. “Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene.” Mendeleev Communications, vol. 25, no. 4, Jul. 2015, pp. 260-261. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.008.

Abstract

Lead tetraacetate oxidation of pyrene followed by hydrolysis affords 1-hydroxypyrene whose esterification with 4-azidobenzoic acid gives a new bifunctional luminophore characterized by UV and luminescence spectroscopy.

References

1.
Barabanov I.I., Pritchina E.A., Takaya T., Gritsan N.P.
Mendeleev Communications, 2008
2.
Competitive singlet-singlet energy transfer and electron transfer activation of aryl azides: application to photo-cross-linking experiments
Shields C.J., Falvey D.E., Schuster G.B., Buchardt O., Nielsen P.E.
Journal of Organic Chemistry, 1988
3.
M. I. Dobrikov, S.A. Gaidamakov, A.A. Koshkin and V. V. Vlasov, Dokl. Akad. Nauk, 1996, 351, 687.(in Russian).
4.
Refined High-Field NMR Solution Structure of a Binary-Addressed Pyrene/Perfluoro-Azide Complementary DNA Oligonucleotide System Shows Extensive Distortion in the Central Nick Region
7.
Excited-State Dynamics in the Covalently Linked Systems: Pyrene−(CH2)n−Aryl Azide
Gritsan N.P., Pritchina E.A., Barabanov I.I., Burdzinski G.T., Platz M.S.
Journal of Physical Chemistry C, 2009
9.
W. H. Gumprecht, Org. Synth., 1973, coll. vol. 5, 632;
10.
3-HYDROXYPYRENE
Organic Syntheses, 1968
11.
W. Kern, U.S. Patent, 2018792, 1935.
12.
10.1016/j.mencom.2015.07.008_sbref0045d
Mataka
Rep. Inst. Adv. Mat. Study, 1996
13.
Pyrene-derived novel one- and two-component organogelators.
Babu P., Sangeetha N.M., Vijaykumar P., Maitra U., Rissanen K., Raju A.R.
Chemistry - A European Journal, 2003
15.
Pyrene-Labeled Poly(aryl ether) Monodendrons:  Synthesis, Characterization, Diffusion Coefficients, and Photophysical Studies
Riley J.M., Alkan S., Chen A., Shapiro M., Khan W.A., Murphy, W.R., Hanson J.E.
Macromolecules, 2001
16.
Methylation of Aromatic Nitro Compounds with Lead Tetraacetate
Fieser L.F., Clapp R.C., Daudt W.H.
Journal of the American Chemical Society, 1942
17.
Improved synthesis of benzo[a]pyren-1-ol and isolation of a covalent benzo[a]pyrene–lead compound
Harvey R.G., Cho H.
Journal of the Chemical Society Chemical Communications, 1975
18.
10.1016/j.mencom.2015.07.008_bib0060
El-Bayoumy
Cancer Res, 1983
19.
Immunochemical detection of metabolites of parent and nitro polycyclic aromatic hydrocarbons in urine samples from persons occupationally exposed to diesel exhaust
Scheepers P.T., Fijneman P.H., Beenakkers M.F., de Lepper A.J., Thuis H.J., Stevens D., Van Rooij J.G., Noordhoek J., Bos R.P.
Fresenius Journal of Analytical Chemistry, 1995
20.
Photochemical instability of 1-nitropyrene, 3-nitrofluoranthene, 1,8-dinitropyrene and their parent polycyclic aromatic hydrocarbons.
Holloway M.P., Biaglow M.C., McCoy E.C., Anders M., Rosenkranz H.S., Howard P.C.
Mutation Research/Genetic Toxicology, 1987
21.
A CONVENIENT METHOD FOR THE SYNTHESIS OF CARBOXYLIC ESTERS
Mukaiyama T., Usui M., Shimada E., Saigo K.
Chemistry Letters, 1975
22.
10.1016/j.mencom.2015.07.008_bib0080
Birks
Photophysics of Aromatic Molecules, 1969