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

Journal Mendeleev Communications
ISSN: 0959-9436
Output data Year: 2015, Volume: 25, Number: 4, Pages: 260-261 Pages count : DOI: 10.1016/j.mencom.2015.07.008
Authors Barabanov Igor I. 1 , Polukhin Alexander V. 1 , Korolev Valerii V. 1,2 , Kuibida Leonid V. 1,2 , Nefedov Andrey A. 2,3
Affiliations
1 (Данные Web of science) Russian Acad Sci, VV Voevodsky Inst Chem Kinet & Combust, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
3 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

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.
Cite: 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. V.25. N4. P.260-261. DOI: 10.1016/j.mencom.2015.07.008 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Jul 1, 2015
Identifiers:
Web of science: WOS:000360416600008
Scopus: 2-s2.0-84938680552
Elibrary: 23996299
OpenAlex: W1629053122
Citing:
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Web of science 1
Scopus 1
Elibrary 1
OpenAlex 1
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