Просмотреть запись

(1-(4-(5-Phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-Bisfunctionalized 3- and 4-PEG: Synthesis and Photophysical Studies

Электронный научный архив УРФУ

Информация об архиве | Просмотр оригинала
 
 
Поле Значение
 
Заглавие (1-(4-(5-Phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-Bisfunctionalized 3- and 4-PEG: Synthesis and Photophysical Studies
 
Автор Mohammed, M. S.
Kovalev, I. S.
Slovesnova, N. V.
Sadieva, L. K.
Platonov, V. A.
Kim, G. A.
Aluru, R.
Novikov, A. S.
Taniya, O. S.
Charushin, V. N.
 
Тематика BOLA MOLECULES
FLUORESCENCE
FLUORESCENCE QUENCHING
HG2+
NITRO-EXPLOSIVE COMPONENTS
OXADIAZOLE
PEGS
PENTAERYTHRITOL TETRANITRATE
SENSOR
“CLICK” REACTIONS
EXPLOSIVE
TRINITROTOLUENE
EXPLOSIVE AGENTS
TRINITROTOLUENE
 
Описание Two new azaheterocycle-based bolas, such as (1-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-bisfunctionalized PEGs, were prepared via Cu-catalyzed click reaction between 2-(4-azidophenyl)-5-(aryl)-oxadiazole-1,3,4 and terminal ethynyls derived from PEG-3 and PEG-4. Due to the presence of two heteroaromatic cores and a PEG linker, these bola molecules are considered as promising fluorescent chemosensors for electron-deficient species. As a result of a well-pronounced “turn-off” fluorescence response towards common nitro-explosive components, such as 2,4-dinitrotoluene (DNT) and 2,4,6-trinitrotoluene (TNT), hard-to-detect pentaerythritol tetranitrate (PETN), as well as Hg2+ cation was observed. © 2023 by the authors.
Russian Academy of Sciences, РАН; Ministry of Education and Science of the Russian Federation, Minobrnauka: 075-15-2022-1118; RUDN University
The quantum chemical calculations were supported by the RUDN University Strategic Academic Leadership Program; the absolute quantum yields were measured using the equipment of the Center for Joint Use “Spectroscopy and Analysis of Organic Compounds” at the Postovsky Institute of Organic Synthesis of the Russian Academy of Sciences (Ural Branch).
This research was funded by the Ministry of Science and Higher Education of the Russian Federation (Reference # 075-15-2022-1118, dated 29 June 2022).
 
Дата 2024-04-05T16:28:05Z
2024-04-05T16:28:05Z
2023
 
Тип Article
Journal article (info:eu-repo/semantics/article)
|info:eu-repo/semantics/publishedVersion
 
Идентификатор Mohammed, MS, Kovalev, IS, Slovesnova, NV, Sadieva, LK, Platonov, VA, Kim, GA, Aluru, R, Novikov, AS, Taniya, OS & Charushin, VN 2023, '(1-(4-(5-Phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-Bisfunctionalized 3- and 4-PEG: Synthesis and Photophysical Studies', Molecules, Том. 28, № 13, 5256. https://doi.org/10.3390/molecules28135256
Mohammed, M. S., Kovalev, I. S., Slovesnova, N. V., Sadieva, L. K., Platonov, V. A., Kim, G. A., Aluru, R., Novikov, A. S., Taniya, O. S., & Charushin, V. N. (2023). (1-(4-(5-Phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-Bisfunctionalized 3- and 4-PEG: Synthesis and Photophysical Studies. Molecules, 28(13), [5256]. https://doi.org/10.3390/molecules28135256
1420-3049
Final
All Open Access, Gold, Green
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85164843919&doi=10.3390%2fmolecules28135256&partnerID=40&md5=16403e33c88c0989509b05254b581003
https://www.mdpi.com/1420-3049/28/13/5256/pdf?version=1688729188
http://elar.urfu.ru/handle/10995/130640
10.3390/molecules28135256
85164843919
001030864500001
 
Язык en
 
Права Open access (info:eu-repo/semantics/openAccess)
cc-by
https://creativecommons.org/licenses/by/4.0/
 
Формат application/pdf
 
Издатель Multidisciplinary Digital Publishing Institute (MDPI)
 
Источник Molecules
Molecules