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NMR and EPR Trapping of the Active Species in the Ethylene Polymerization and Trimerization Catalyst Systems Научная публикация

Журнал Catalysis for Sustainable Energy
ISSN: 2084-6819
Вых. Данные Год: 2016, Том: 3, Номер: 1, Страницы: 15-24 Страниц : 10 DOI: 10.1515/cse-2016-0004
Ключевые слова Ethylene; Intermediate; Mechanism, NMR and EPR; Polymerization; Post-metallocene
Авторы Soshnikov I.E. 1,2 , Semikolenova N.V. 1 , Antonov A.A. 1,2 , Bryliakov K.P. 1,2 , Zakharov V.A. 1,2 , Talsi E.P. 2
Организации
1 Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090, Russian Federation
2 Novosibirsk State University, Pirogova 2, Novosibirsk 630090, Russian Federation

Информация о финансировании (2)

1 Российский фонд фундаментальных исследований 16-53-53014
2 Российский фонд фундаментальных исследований 16-03-00236

Реферат: In this work, previously undetected intermediates of several practically promising catalyst systems for ethylene polymerization and trimerization are discussed. In particular, the activation of ethylene polymerization catalysts (1) LNiCl2 (L = 2,4,6-trimethyl- (N-5,6,7-trihydroquinolin-8-ylidene)phenylamine) with AlEt2Cl and AlMe2Cl, (2) activation of bis(imino)pyridine vanadium(III) chloride L1VIIICl3 (L1 = 2,6-(ArN=CMe)2C5H3N, Ar = 2,6-iPr2C6H3; 2,6-Me2C6H3; 2,4,6-Me3C6H2; 3,5- F2C6H3) with AlMe3/[Ph3C]+[B(C6F5)]4¯ and MAO, and (3) selective ethylene trimerization catalyst (FI)TiCl3 (FI = phenoxyimine ligand with an additional aryl-OCH3 donor) with MAO have been assessed by NMR and EPR spectroscopy. The nature of ion-pair intermediates – the closest precursors of the propagating species – has been established, and the major catalyst deactivation pathways are discussed.
Библиографическая ссылка: Soshnikov I.E. , Semikolenova N.V. , Antonov A.A. , Bryliakov K.P. , Zakharov V.A. , Talsi E.P.
NMR and EPR Trapping of the Active Species in the Ethylene Polymerization and Trimerization Catalyst Systems
Catalysis for Sustainable Energy. 2016. V.3. N1. P.15-24. DOI: 10.1515/cse-2016-0004 РИНЦ CAPlus OpenAlex
Файлы: Полный текст от издателя
Даты:
Опубликована в печати: 30 янв. 2016 г.
Поступила в редакцию: 26 мая 2016 г.
Принята к публикации: 12 июл. 2016 г.
Опубликована online: 30 сент. 2016 г.
Идентификаторы БД:
РИНЦ: 30676791
Chemical Abstracts: 2018:1414169
OpenAlex: W2587594161
Цитирование в БД:
БД Цитирований
РИНЦ 1
Альметрики: