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Design of postmetallocene catalytic systems of arylimine type for olefin polymerization: XVII. Synthesis of methoxy-substituted (p-aryl)salicylaldimines containing omega-alkenyloxy group, and their complexes with titanium(IV) dichloride Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2014, Volume: 50, Number: 11, Pages: 1565-1572 Pages count : 8 DOI: 10.1134/S1070428014110050
Authors Oleinik I.I. 1 , Oleinik I.V. 1 , Ivanchev S.S. 2 , Tolstikov G.A. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Branch, Boreskov Inst Catalysis, St Petersburg Div, St Petersburg 196140, Russia

Abstract: Reaction of 5-methoxy-substituted salicylic aldehydes containing in the position 3 tert-butyl, 2-phenylpropan-2-yl, or 1-phenylethyl groups with m- and p-allyloxy-, (but-3-enyloxy)-, (pent-4-enyloxy)anilines without solvent in an open system at 130A degrees C afforded a series of (N-aryl)salicylaldimines L that with TiCl2 (OPr-i)(2) formed complexes of titanium(IV) dichloride L2TiCl2.
Cite: Oleinik I.I. , Oleinik I.V. , Ivanchev S.S. , Tolstikov G.A.
Design of postmetallocene catalytic systems of arylimine type for olefin polymerization: XVII. Synthesis of methoxy-substituted (p-aryl)salicylaldimines containing omega-alkenyloxy group, and their complexes with titanium(IV) dichloride
Russian Journal of Organic Chemistry. 2014. V.50. N11. P.1565-1572. DOI: 10.1134/S1070428014110050 WOS Scopus РИНЦ OpenAlex
Original: Олейник И.И. , Олейник И.В. , Иванчев С.С. , Толстиков Г.А.
Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов. xvii. синтез метоксизамещенных ( n-арил)салицилальдиминов, содержащих ω-алкенилоксигруппу, и комплексов дихлорида титана(iv) на их основе
Журнал органической химии (RUSS J ORG CHEM+). 2014. Т.50. №11. С.1581-1588. РИНЦ
Dates:
Published print: Nov 1, 2014
Published online: Dec 17, 2014
Identifiers:
Web of science: WOS:000346494700005
Scopus: 2-s2.0-84919687406
Elibrary: 24021478
OpenAlex: W2068361924
Citing:
DB Citing
Web of science 3
Scopus 3
Elibrary 6
OpenAlex 3
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