A Quantum Chemical Study of the Molecular Structure of Active Centers and Growth in Ethylene Polymerization in the Catalytic System LFeCl2/AlMe3 (L = 2,6-Bis-Iminopyridyl) Научная публикация
Журнал |
Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210 |
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Вых. Данные | Год: 2004, Том: 45, Номер: 4, Страницы: 508-518 Страниц : 11 DOI: 10.1023/B:KICA.0000038078.16393.2e | ||
Ключевые слова | Pyridyl; Quantum Chemical Study; Ethylene Polymerization; Perpendicular Plane; AlMe3 | ||
Авторы |
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Организации |
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Информация о финансировании (1)
1 | International Association for the Promotion of Co-operation with Scientists from the New Independent States of the Former Soviet Union | 00-00841 |
Реферат:
Density functional theory with hybrid exchange-correlation functional B3P86 is used to calculate the molecular structures of neutral Fe(II) complexes formed in the LFeCl2/AlMe3 system (L = tridentate bis(imine)pyridyl ligand). A simplified model of the LFeCl2 complex is used in calculations, where L is replaced by three NH3 ligands. Parameters of geometric and electronic structures of the complexes (NH3)3FeMe(μ-Me)AlMe3 (I) and (NH3)3FeMe(μ-Me)2AlMe2 (IIA and IIB), which are the structures where the Fe-Me and Fe-μ-Me groups are in one or two perpendicular planes, respectively, were determined. Complexes II, which were earlier identified using 1H NMR spectroscopy, are more stable than complex I. Complex IIB is strongly polarized (the distances r(Fe-μ-Me) and r(Al-μ-Me) are 3.70 and 2.08 Å, respectively) and coordinatively unsaturated due to the transfer of the methyl group from (NH3)3FeMe2 onto AlMe3. It has significant electron density deficit in the coordination sphere of the transition metal [(NH3)3FeMe] Q (Q = +0.80e). The energetic profile of the reaction of ethylene addition to the Fe-Me bond for the complexes (NH3)3FeMe2, IIA and IIB, was calculated. It was shown that, compared to (NH3)3FeMe2, a drastic decrease in the activation energy of ethylene addition is observed in the case of IIB (from 135 to 66 kJ/mol). The reason for the more efficient activation of the complexes LFeMe2 by a weak Lewis acid (AlMe3) and for the increased reactivity of the metal-alkyl bond in complex IIB compared to the zirconocene complex Cp2ZrMe2 is discussed.
Библиографическая ссылка:
Zakharov I.I.
, Zakharov V.A.
A Quantum Chemical Study of the Molecular Structure of Active Centers and Growth in Ethylene Polymerization in the Catalytic System LFeCl2/AlMe3 (L = 2,6-Bis-Iminopyridyl)
Kinetics and Catalysis. 2004. V.45. N4. P.508-518. DOI: 10.1023/B:KICA.0000038078.16393.2e WOS Scopus РИНЦ
A Quantum Chemical Study of the Molecular Structure of Active Centers and Growth in Ethylene Polymerization in the Catalytic System LFeCl2/AlMe3 (L = 2,6-Bis-Iminopyridyl)
Kinetics and Catalysis. 2004. V.45. N4. P.508-518. DOI: 10.1023/B:KICA.0000038078.16393.2e WOS Scopus РИНЦ
Оригинальная версия:
Захаров И.И.
, Захаров В.А.
Квантово-химическое исследование молекулярной структуры активных центров и реакции роста при полимеризации этилена на каталитической системе LFeCl2/AlMe3 (L = 2,6-бис-иминопиридил)
Кинетика и катализ. 2004. Т.45. №4. С.540-550. РИНЦ
Квантово-химическое исследование молекулярной структуры активных центров и реакции роста при полимеризации этилена на каталитической системе LFeCl2/AlMe3 (L = 2,6-бис-иминопиридил)
Кинетика и катализ. 2004. Т.45. №4. С.540-550. РИНЦ
Даты:
Поступила в редакцию: | 20 янв. 2003 г. |
Опубликована в печати: | 1 июл. 2004 г. |
Идентификаторы БД:
Web of science | WOS:000223776200008 |
Scopus | 2-s2.0-4444244903 |
РИНЦ | 14399035 |
Chemical Abstracts | 2004:671526 |
Chemical Abstracts (print) | 142:156357 |
OpenAlex | W1997312360 |