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Lewis Base Adducts of Phosphine-Stabilized Pb(II) Cations: Synthesis and Catalytic Hydroamination of Alkynes Научная публикация

Журнал Inorganic Chemistry
ISSN: 0020-1669 , E-ISSN: 1520-510X
Вых. Данные Год: 2022, Том: 61, Номер: 40, Страницы: 16156-16162 Страниц : 7 DOI: 10.1021/acs.inorgchem.2c02727
Авторы Chandran Aswin 1 , Léon Baeza José Miguel 2,1 , Timofeeva Vladislava 1,3 , Nougué Raphael 1 , Takahashi Shintaro 1 , Ohno Ryoma 4 , Baceiredo Antoine 1 , Rojas Guerrero Rene Segundo 2 , Syroeshkin Mikhail 3 , Matsuo Tsukasa 4 , Saffon-Merceron Nathalie 5 , Kato Tsuyoshi 1
Организации
1 Laboratoire Hétérochimie Fondamentale et Appliquée (UMR 5069), Université de Toulouse, CNRS, 118 route de Narbonne, F-31062 Toulouse, France
2 Departamento de Química Inorganica, Facultad de Química, Pontificia Universidad Catolica de Chile, Casilla 306, Santiago 3580000, Chile
3 N. D. Zelinsky Institute of Organic Chemistry, Leninsky prosp. 47, 119991 Moscow, Russia
4 Department of Applied Chemistry, Faculty of Science and Engineering, Kindai University, 3-4-1 Kowakae, Higashi-Osaka, Osaka 577-8502, Japan
5 Institut de Chimie de Toulouse (UAR 2599), Université de Toulouse, CNRS, 118 route de Narbonne, F-31062 Toulouse, France

Реферат: Phosphine-stabilized Pb(II) cations, generated by chloride abstraction from chloroplumbylene 1, readily react with Lewis bases (L) such as phosphines and amines to give the corresponding donor–acceptor complexes 3. These complexes 3 react with phenylacetlylene via alkyne insertion into the Pb–L bond to afford the corresponding vinylplumbylenes 4. Of particular interest, the stable complex 4-HNiPr2 (with a secondary amine) can be used as a hydroamination catalyst of phenylacetylene.
Библиографическая ссылка: Chandran A. , Léon Baeza J.M. , Timofeeva V. , Nougué R. , Takahashi S. , Ohno R. , Baceiredo A. , Rojas Guerrero R.S. , Syroeshkin M. , Matsuo T. , Saffon-Merceron N. , Kato T.
Lewis Base Adducts of Phosphine-Stabilized Pb(II) Cations: Synthesis and Catalytic Hydroamination of Alkynes
Inorganic Chemistry. 2022. V.61. N40. P.16156-16162. DOI: 10.1021/acs.inorgchem.2c02727 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000868142200001
Scopus: 2-s2.0-85139433197
OpenAlex: W4297961903
Цитирование в БД:
БД Цитирований
OpenAlex 9
Scopus 10
Web of science 9
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