Palanquin-Like Cu4Na4 Silsesquioxane Synthesis (via Oxidation of 1,1-bis(Diphenylphosphino)methane), Structure and Catalytic Activity in Alkane or Alcohol Oxidation with Peroxides

Palanquin-Like Cu4Na4 Silsesquioxane Synthesis (via Oxidation of 1,1-bis(Diphenylphosphino)methane), Structure and Catalytic Activity in Alkane or Alcohol Oxidation with Peroxides Научная публикация

Журнал

Catalysts
ISSN: 2073-4344

Вых. Данные

Год: 2019, Том: 9, Номер: 2, Номер статьи : 154, Страниц : 13 DOI: 10.3390/catal9020154

Авторы

Kulakova Alena N. ^1,2 , Khrustalev Victor N. ^2,3 , Zubavichus Yan V. ^3,4 , Shul’pina Lidia S. ¹ , Shubina Elena S. ¹ , Levitsky Mikhail M. ¹ , Ikonnikov Nikolay S. ¹ , Bilyachenko Nikolay S. ^1,2 , Kozlov Yuriy N. ^5,6 , Shul'pin Georgiy B. ^2,5,6

Организации

1	Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova, 28, Moscow 119991, Russia
2	People’s Friendship University of Russia, ul. Miklukho-Maklaya, dom 6, Moscow 117198, Russia
3	National Research Center “Kurchatov Institute”, pl. Akad. Kurchatova, dom 1, Moscow 123182, Russia
4	Boreskov Institute of Catalysis SB RAS, prosp. Akad. Lavrentieva, dom 5, Novosibirsk 630090, Russia
5	Semenov Institute of Chemical Physics, Russian Academy of Sciences, ul. Kosygina, dom 4, Moscow 119991, Russia
6	Chair of Chemistry and Physics, Plekhanov Russian University of Economics, Stremyannyi pereulok, dom 36, Moscow 117997, Russia

The self-assembly synthesis of copper-sodium phenylsilsesquioxane in the presence of 1,1-bis(diphenylphosphino)methane (dppm) results in an unprecedented cage-like product: [(PhSiO1,5)6]2[CuO]4[NaO0.5]4[dppmO2]2 1. The most intriguing feature of the complex 1 is the presence of two oxidized dppm species that act as additional O-ligands for sodium ions. Two cyclic phenylsiloxanolate (PhSiO1,5)6 ligands coordinate in a sandwich manner with the copper(II)-containing layer of the cage. The structure of 1 was established by X-ray diffraction analysis. Complex 1 was shown to be a very good catalyst in the oxidation of alkanes and alcohols with hydrogen peroxide or tert-butyl hydroperoxide in acetonitrile solution. Thus, cyclohexane (CyH), was transformed into cyclohexyl hydroperoxide (CyOOH), which could be easily reduced by PPh3 to afford stable cyclohexanol with a yield of 26% (turnover number (TON) = 240) based on the starting cyclohexane. 1-Phenylethanol was oxidized by tert-butyl hydroperoxide to give acetophenone in an almost quantitative yield. The selectivity parameters of the oxidation of normal and branched alkanes led to the conclusion that the peroxides H2O2 and tert-BuOOH, under the action of compound (1), decompose to generate the radicals HO• and tert-BuO• which attack the C-H bonds of the substrate.

Kulakova A.N. , Khrustalev V.N. , Zubavichus Y.V. , Shul’pina L.S. , Shubina E.S. , Levitsky M.M. , Ikonnikov N.S. , Bilyachenko N.S. , Kozlov Y.N. , Shul'pin G.B.
Palanquin-Like Cu4Na4 Silsesquioxane Synthesis (via Oxidation of 1,1-bis(Diphenylphosphino)methane), Structure and Catalytic Activity in Alkane or Alcohol Oxidation with Peroxides

Catalysts. 2019. V.9. N2. 154 :1-13. DOI: 10.3390/catal9020154 WOS Scopus РИНЦ CAPlus OpenAlex Sciact

Полный текст от издателя

Поступила в редакцию:	26 дек. 2018 г.
Принята к публикации:	16 янв. 2019 г.
Опубликована online:	4 февр. 2019 г.
Опубликована в печати:	1 мар. 2019 г.

Web of science:	WOS:000460702200048
Scopus:	2-s2.0-85062496562
РИНЦ:	38678435
Chemical Abstracts:	2019:389618
OpenAlex:	W2912354340
Sciact:	31664

БД	Цитирований
Scopus	26
OpenAlex	28