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Anthracene-Based Cyclophanes with Selective Fluorescent Responses for TTP and GTP: Insights into Recognition and Sensing Mechanisms Научная публикация

Журнал Chemistry - A European Journal
ISSN: 0947-6539 , E-ISSN: 1521-3765
Вых. Данные Год: 2019, Том: 25, Номер: 14, Страницы: 3541-3549 Страниц : 9 DOI: 10.1002/chem.201806130
Ключевые слова fluorescence; host–guest systems; macrocycles; nucleotide recognition; receptors; sensors
Авторы Agafontsev A.M. 1,2,3 , Shumilova T.A. 1 , Ruffer T. 1 , Lang H. 1 , Kataev E.A. 1
Организации
1 (Scopus) Institute of Chemistry, Technische Universit?t Chemnitz, Chemnitz, 09107, Germany
2 (Scopus) N.N. Vorozhtsov Institute of Organic Chemistry SB RAS, 9 Lavrentiev Avenue, Novosibirsk, 630090, Russian Federation
3 (Scopus) Novosibirsk State University, Pirogova St. 1, Novosibirsk, 630090, Russian Federation

Реферат: Three anthracene-based cyclophanes were synthesized and their binding properties towards nucleoside triphosphates were studied. A new polycyclic amine derived from dearomatized anthracene was identified as a major side product in the cyclization reaction between 9,10-anthracenedicarboxaldehyde and diethylenetriamine. Its structure was determined by single-crystal X-ray analysis. The cyclophanes were found to form 1:1 complexes with all nucleoside triphosphates as well as with pyrophosphate in a buffered aqueous solution at pH 6.2. A turn-on fluorescence response was observed for all nucleotides except for GTP, which demonstrated strong fluorescence quenching. The strongest turn-on fluorescence was observed for the largest receptor 3 in the presence of thymidine triphosphate (TTP). Based on the NMR and fluorescence experiments, two major binding modes for nucleotide complexes were identified. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Библиографическая ссылка: Agafontsev A.M. , Shumilova T.A. , Ruffer T. , Lang H. , Kataev E.A.
Anthracene-Based Cyclophanes with Selective Fluorescent Responses for TTP and GTP: Insights into Recognition and Sensing Mechanisms
Chemistry - A European Journal. 2019. V.25. N14. P.3541-3549. DOI: 10.1002/chem.201806130 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована online: 19 февр. 2019 г.
Опубликована в печати: 7 мар. 2019 г.
Идентификаторы БД:
Web of science: WOS:000460692100018
Scopus: 2-s2.0-85061919443
РИНЦ: 38649069
OpenAlex: W2909358018
Цитирование в БД:
БД Цитирований
Scopus 13
Web of science 11
OpenAlex 12
Альметрики: