When Applying the Mercury Poisoning Test to Palladacycle-Catalyzed Reactions, One Should Not Consider the Common Misconception of Mercury(0) Selectivity

The aim of this study was to demonstrate the absolute necessity of control experiments for a correct interpretation of mercury drop test results when applied to mechanistic studies of palladacycle-catalyzed reactions. It was shown that the interaction of diverse azapalladacycles with metallic mercury leads to the formation of organomercuric chlorides during the redox-transmetalation process. The structure of these organomercurials was confirmed by elemental analysis, 1H, 13C{1H}, and 199Hg{1H} NMR spectra, X-ray diffraction analysis, and DFT calculations. The behavior and properties of C,N-mercuracycles bearing the weak and labile N···Hg bond are discussed on the basis of the temperature dependence of the NMR spectra and calculated thermodynamic parameters of the dechelation process. © 2018 American Chemical Society.

Авторы
Gorunova O.N.1 , Novitskiy I.M.2 , Grishin Y.K.2 , Gloriozov I.P.2 , Roznyatovsky V.A.2 , Khrustalev V.N. 3, 4 , Kochetkov K.A.1 , Dunina V.V.2
Журнал
Издательство
American Chemical Society
Номер выпуска
17
Язык
Английский
Страницы
2842-2858
Статус
Опубликовано
Том
37
Год
2018
Организации
  • 1 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciencies, Vavilova St. 28, Moscow, 119991, Russian Federation
  • 2 Department of Chemistry, M. V. Lomonosov Moscow State University, Lenin Hills, Moscow, 119991, Russian Federation
  • 3 Inorganic Chemistry Department, Peoples' Friendship University of Russia, Miklukho-Maklay Street 6, Moscow, 117198, Russian Federation
  • 4 National Research Center, Kurchatov Institute, Acad. Kurchatov Sq. 1, Moscow, 123182, Russian Federation
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6420/
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