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Study of the Supported Zirconocene Catalysts by Means of UV/vis and DRIFT Spectroscopy Full article

Journal Journal of Molecular Catalysis A: Chemical
ISSN: 1381-1169
Output data Year: 2005, Volume: 240, Number: 1-2, Pages: 33-39 Pages count : 7 DOI: 10.1016/j.molcata.2005.06.034
Tags DRIFTS, DRS, Supported zirconocene catalysts, TIBA, UV/vis
Authors Panchenko V.N. 1 , Zakharov V.A. 1 , Paukshtis E.A. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch of Russian Academy of Sciences

Abstract: UV/vis in diffusion reflection mode (DRS) and DRIFT spectroscopy have been used to study the surface zirconocene species formed at the interaction of Me2Si(Ind)2ZrCl2 and Me2Si(Ind)2ZrMe2 complexes with the MAO/SiO2 support. Effect of additional activation of these catalysts with TIBA has been studied as well. Structure of type [Me2Si(Ind)2ZrMe]+[MeMAO]− (C) is formed at the reaction of Me2Si(Ind)2ZrMe2 complex with MAO/SiO2 (a.b. at 456 nm in UV/vis spectra). Interaction of this complex with TIBA results in the formation of new structure (D) with a.b. at 496 nm in UV/vis spectra. The surface species of different composition and structures are formed at interaction of Me2Si(Ind)2ZrCl2 complex with MAO/SiO2. The ratio between these species depends on the zirconium content in the Me2Si(Ind)2ZrCl2/MAO/SiO2 catalysts. According to the DRIFTS data (CO and ethylene adsorption) and ethylene polymerization data these catalysts contain active Zrsingle bondMe bonds but activity of these catalysts at ethylene polymerization is low. Interaction of Me2Si(Ind)2ZrCl2/MAO/SiO2 with TIBA leads to the formation of the new cationic structure of type (D) with a.b. at 496 nm in UV/vis spectra and great increasing of activity at ethylene polymerization.
Cite: Panchenko V.N. , Zakharov V.A. , Paukshtis E.A.
Study of the Supported Zirconocene Catalysts by Means of UV/vis and DRIFT Spectroscopy
Journal of Molecular Catalysis A: Chemical. 2005. V.240. N1-2. P.33-39. DOI: 10.1016/j.molcata.2005.06.034 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jul 23, 2004
Accepted: Jun 22, 2005
Published online: Jul 26, 2005
Published print: Oct 3, 2005
Identifiers:
Web of science: WOS:000231930500006
Scopus: 2-s2.0-24144450350
Elibrary: 13476859
Chemical Abstracts: 2005:959386
Chemical Abstracts (print): 144:370460
OpenAlex: W2075764683
Citing:
DB Citing
Web of science 15
Scopus 16
Elibrary 16
OpenAlex 6
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