Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/111952
Title: Asymmetrically Functionalized 1,3-Di(2-pyridyl)benzenes: Synthesis and Photophysical Studies
Authors: Starnovskaya, E. S.
Kopchuk, D. S.
Shtaitz, Y. K.
Savchuk, M. I.
Nikonov, I. L.
Egorov, I. N.
Zyryanov, G. V.
Rusinov, V. L.
Chupakhin, O. N.
Issue Date: 2022
Publisher: Springer
Springer Science and Business Media LLC
Citation: Asymmetrically Functionalized 1,3-Di(2-pyridyl)benzenes: Synthesis and Photophysical Studies / E. S. Starnovskaya, D. S. Kopchuk, Y. K. Shtaitz et al. // Journal of Fluorescence. — 2022. — Vol. 32. — Iss. 1. — P. 125-133.
Abstract: A convenient synthetic approach to asymmetrically functionalized 1,3-di(2-pyridyl)benzenes starting from 3-(3-bromophenyl)-1,2,4-triazines using sequential aza-Diels–Alder reactions and Stille cross-coupling is reported. Photophysical properties of the obtained compounds are studied. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Keywords: 1,2,4-TRIAZINES
1,3-DI(2-PYRIDYL)BENZENES
AZA-DIELS–ALDER REACTION
CROSS-COUPLING
FLUORESCENCE
BENZENE
CHEMICAL REACTIONS
1,2,4-TRIAZINE
1,3-DI(2-PYRIDYL)BENZENE
AZA-DIELS–ALDER REACTION
CROSS-COUPLINGS
DIELS-ALDER REACTION
FUNCTIONALIZED
PHOTOPHYSICAL STUDIES
PYRIDYL
STILLE CROSS-COUPLING
SYNTHETIC APPROACH
FLUORESCENCE
ARTICLE
DIELS ALDER REACTION
FLUORESCENCE
STILLE REACTION
SYNTHESIS
URI: http://hdl.handle.net/10995/111952
Access: info:eu-repo/semantics/openAccess
SCOPUS ID: 85116515008
PURE ID: 29378886
ISSN: 1053-0509
metadata.dc.description.sponsorship: This work was supported by Russian Science Foundation (Grant № 19-73-10144) and Grants Council of the President of the Russian Federation (no. NSh-2700.2020.3). No other sources of funding were involved.
RSCF project card: 19-73-10144
Appears in Collections:Научные публикации, проиндексированные в SCOPUS и WoS CC

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