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Mechanistic Investigation and New Catalyst Design in Palladium- and Platinum-Catalyzed Se−Se Bond Addition to Alkynes Научная публикация

Журнал Organometallics
ISSN: 1520-6041 , E-ISSN: 0276-7333
Вых. Данные Год: 2003, Том: 22, Номер: 7, Страницы: 1414-1421 Страниц : 8 DOI: 10.1021/om0205391
Авторы Ananikov Valentine P. 1 , Beletskaya Irina P. 2 , Aleksandrov Grigory G. 3 , Eremenko Igor L. 3
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Leninsky Prospect 47, Moscow 119991, Russia
2 M. V. Lomonosov Moscow State University, Moscow 119899, Russia
3 N. S. Kurnakov Institute of General and Inorganic Chemistry, Leninsky Prospect 31, Moscow 117907, Russia

Реферат: The present study explains the different catalytic activities of platinum and palladium in Se−Se addition reactions with alkynes. Under the catalytic conditions cis-[Pt(SePh)2(PPh3)2] undergoes fast isomerization to the trans isomer, which does not react with alkynes. Palladium complexes maintain their catalytic activity, due to the formation of the dinuclear structure [Pd2(SePh)4(PPh3)2]. It was shown that the palladium intermediate involved in the catalytic cycle can be prepared directly in the reaction mixture starting from the simple [PdCl2(PPh3)2] precursor, thus allowing replacement for the traditional Pd(PPh3)4 catalyst. X-ray analysis shows that the products of Se−Se addition reactions with alkynes possess the necessary geometry parameters for coordination as bidentate ligands.
Библиографическая ссылка: Ananikov V.P. , Beletskaya I.P. , Aleksandrov G.G. , Eremenko I.L.
Mechanistic Investigation and New Catalyst Design in Palladium- and Platinum-Catalyzed Se−Se Bond Addition to Alkynes
Organometallics. 2003. V.22. N7. P.1414-1421. DOI: 10.1021/om0205391 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000181902400012
Scopus: 2-s2.0-0037474822
OpenAlex: W2035195284
Цитирование в БД:
БД Цитирований
OpenAlex 96
Scopus 104
Web of science 97
Альметрики: