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Highly Active Iron and Cobalt Catalysts for the Polymerization of Ethylene

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This article is published in Journal of the American Chemical Society.The article was published on 1998-04-14. It has received 1378 citations till now. The article focuses on the topics: Polymerization & Cobalt.

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Iron-Catalyzed Reactions in Organic Synthesis

TL;DR: A new iron(III) halide-promoted aza-Prins cyclization between γ,δ-unsaturated tosylamines and aldehydes provides six-membered azacycles in good to excellent yields.
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Catalytic activities of Schiff base transition metal complexes

TL;DR: A review of the catalytic activity of metal complexes of binaphthyl compounds and their combinations with salen Schiff base is presented in this paper, where the pyridyl bis (imide) and pyridine bis(imine) complexes of cobalt(II), iron(II) ions have been used as catalysts in the polymerization of ethylene and propylene.
References
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Journal ArticleDOI

Stereospecific Olefin Polymerization with Chiral Metallocene Catalysts

TL;DR: In contrast to heterogeneous Ziegler-Natta catalysts, homogeneous metallocene-based catalysts as discussed by the authors allow efficient control of regio-and stereoregularities, molecular weights and molecular weight distributions, and comonomer incorporation.
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Cationic zirconocene olefin polymerization catalysts based on the organo-Lewis acid tris(pentafluorophenyl)borane. A synthetic, structural, solution dynamic, and polymerization catalytic study

TL;DR: In this article, the structural and chemical properties of a series of electron-deficient cationic zircocene alkyl and hydrido complexes with high olefin polymerization activities were studied.
Journal ArticleDOI

Cationic Group 4 metallocene complexes and their role in polymerisation catalysis: the chemistry of well defined Ziegler catalysts

TL;DR: In this paper, Cationic alkyl complexes of Group 4 metallocenes of the type [MCp2R]+(M = Ti, Zr or Hf, Cp = C5H5) have been recognized as the catalytically active species in metallocene-based olefin polymerisation catalysts.
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