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Selective Ethylene Dimerization into 2-Butenes Using Homogeneous and Supported Nickel(II) 2-Iminopyridine Catalysts Full article

Conference XI International Conference Mechanisms of Catalytic Reactions
07-11 Oct 2019 , Сочи
Journal Topics in Catalysis
ISSN: 1022-5528 , E-ISSN: 1572-9028
Output data Year: 2020, Volume: 63, Number: 1-2, Pages: 222-228 Pages count : 7 DOI: 10.1007/s11244-019-01208-8
Tags Ethylene, 2-Iminopyridine, Electron-withdrawing, Nickel, 2-Butene, Dimerization
Authors Antonov Artem A. 1,2 , Semikolenova Nina V. 1 , Soshnikov Igor E. 1,2 , Talsi Evgenii P. 1,2 , Bryliakov Konstantin P. 1,2
Affiliations
1 Boreskov Institute of Catalysis
2 Novosibirsk State University

Funding (1)

1 Federal Agency for Scientific Organizations 0303-2016-0009

Abstract: In this work, we report a series of novel nickel(II) dibromide and dichloride complexes with 2-iminopyridine and 2-iminoquinoline ligands bearing electron-withdrawing substituents (F, Cl, CF3), that have demonstrated high ethylene dimerization activity [up to 19.2 × 10^6 g of oligomers·(mol Ni)−1 h−1] in the presence of MAO or Et2AlCl, affording predominantly a mixture of 1-butene and cis- and trans-2-butene (C4 selectivity varies from 89 to 100%; 2-butenes selectivity in the C4 fraction approaches 96%). The effects of ligand substituents and the cocatalyst nature on the activity and selectivity of the nickel(II) complexes in ethylene dimerization have been established. Several nickel complexes were supported on silica-alumina and the resulting heterogeneous catalysts were probed towards ethylene dimerization. These catalysts also afford 2-butenes, with the activity and C4 selectivity being comparable to that of homogeneous catalysts.
Cite: Antonov A.A. , Semikolenova N.V. , Soshnikov I.E. , Talsi E.P. , Bryliakov K.P.
Selective Ethylene Dimerization into 2-Butenes Using Homogeneous and Supported Nickel(II) 2-Iminopyridine Catalysts
Topics in Catalysis. 2020. V.63. N1-2. P.222-228. DOI: 10.1007/s11244-019-01208-8 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Published online: Nov 29, 2019
Published print: Mar 17, 2020
Identifiers:
Web of science: WOS:000499200900001
Scopus: 2-s2.0-85075873202
Elibrary: 43214376
Chemical Abstracts: 2019:2271936
Chemical Abstracts (print): 172:290367
OpenAlex: W2989783339
Citing:
DB Citing
Web of science 13
Scopus 12
Elibrary 12
OpenAlex 14
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