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Elevated reaction order of 1,3,5-tri-tert-butylbenzene bromination as evidence of a clustered polybromide transition state: a combined kinetic and computational study Научная публикация

Журнал Organic and Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539
Вых. Данные Год: 2019, Том: 17, Номер: 15, Страницы: 3781-3789 Страниц : 9 DOI: 10.1039/c9ob00607a
Авторы Shernyukov Andrey V. 1,2 , Genaev Alexander M. 1 , Salnikov George E. 1,2,3 , Shubin Vyacheslav G. 1 , Rzepa Henry S. 4
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Acad Lavrentiev Ave 9, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Pirogova 2, Novosibirsk 630090, Russia
3 (Данные Web of science) Int Tomog Ctr, Inst Skaya 3a, Novosibirsk 630090, Russia
4 (Данные Web of science) Imperial Coll London, MSRH, Dept Chem, 80 Wood Lane, London W12 0BZ, England

Реферат: The kinetics and mechanism of concurrent bromo-de-protonation and bromo-de-tert-butylation of 1,3,5-tri-tert-butylbenzene at different bromine concentrations were studied experimentally and theoretically. Both reactions have high order in bromine (experimental kinetic orders similar to 5 and similar to 7, respectively). According to quantum chemical DFT calculations, such high reaction orders are caused by participation of clustered polybromide anions Br-2n-1(-) in transition states. Bromo-de-tert-butylation has a higher order due to its bigger reaction center demanding clusters of extended size. A significant primary deuterium kinetic isotope effect (KIE) for bromo-de-protonation is measured indicating proton removal is rate limiting, as confirmed by computed DFT models. The latter predict a larger value for the KIE than measured and possible explanations for this are discussed.
Библиографическая ссылка: Shernyukov A.V. , Genaev A.M. , Salnikov G.E. , Shubin V.G. , Rzepa H.S.
Elevated reaction order of 1,3,5-tri-tert-butylbenzene bromination as evidence of a clustered polybromide transition state: a combined kinetic and computational study
Organic and Biomolecular Chemistry. 2019. V.17. N15. P.3781-3789. DOI: 10.1039/c9ob00607a WOS Scopus РИНЦ OpenAlex
Идентификаторы БД:
Web of science: WOS:000464584200013
Scopus: 2-s2.0-85064129451
РИНЦ: 38696141
OpenAlex: W2924322755
Цитирование в БД:
БД Цитирований
Web of science 8
Scopus 9
РИНЦ 5
OpenAlex 9
Альметрики: