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Fluorinated and ring-substituted bisbenzimidazole copper complexes for ethylene/acrylate copolymerization

Bisbenzimidazole copper dichloride complexes (CuBBIMs), when activated with methylaluminoxane, catalyze the random copolymerization of ethylene with acrylates to produce highly linear functional copolymers. To probe the sensitivity of the copolymerization to the catalyst structure, a series of CuBBI...

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Published in:Journal of polymer science. Part A, Polymer chemistry Polymer chemistry, 2006-03, Vol.44 (6), p.1817-1840
Main Authors: Baugh, Lisa Saunders, Sissano, Joseph A., Kacker, Smita, Berluche, Enock, Stibrany, Robert T., Schulz, Donald N., Rucker, Steven P.
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cited_by cdi_FETCH-LOGICAL-c3229-e4130f0a4f0a9856b1d23c7f7e638438664e2a344105c38ad1d02cb73f99fbd43
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container_title Journal of polymer science. Part A, Polymer chemistry
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description Bisbenzimidazole copper dichloride complexes (CuBBIMs), when activated with methylaluminoxane, catalyze the random copolymerization of ethylene with acrylates to produce highly linear functional copolymers. To probe the sensitivity of the copolymerization to the catalyst structure, a series of CuBBIM catalysts with various steric, electronic, and geometric ligand characteristics was prepared, including CuBBIMs having benzimidazole ring substituents and ligand backbones of various lengths. Four different acrylates were also evaluated as comonomers (t‐butyl acrylate, methyl acrylate, t‐butyl methacrylate, and methyl methacrylate). Although no obvious ligand‐based influences on copolymerization were identified, the structure of the acrylate comonomer was found to exert significant effects. Copolymers prepared with t‐butyl methacrylate comonomer exhibited the highest ethylene contents (31–63%), whereas those prepared with methyl acrylate contained only minor amounts of ethylene (
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To probe the sensitivity of the copolymerization to the catalyst structure, a series of CuBBIM catalysts with various steric, electronic, and geometric ligand characteristics was prepared, including CuBBIMs having benzimidazole ring substituents and ligand backbones of various lengths. Four different acrylates were also evaluated as comonomers (t‐butyl acrylate, methyl acrylate, t‐butyl methacrylate, and methyl methacrylate). Although no obvious ligand‐based influences on copolymerization were identified, the structure of the acrylate comonomer was found to exert significant effects. Copolymers prepared with t‐butyl methacrylate comonomer exhibited the highest ethylene contents (31–63%), whereas those prepared with methyl acrylate contained only minor amounts of ethylene (&lt;15%). Copolymerizations carried out at lowered acrylate feed levels generally had increased ethylene contents but showed smaller yields, lowered molecular weights, and increased branching. Unusual ketoester structures were also observed in the methyl acrylate and methyl methacrylate containing copolymers, suggesting that the acrylate ester group size may be an important controlling factor for copolymerization. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 1817–1840, 2006 Bisbenzimidazole copper dichloride complexes featuring ligands with various steric, electronic, and geometric characteristics were prepared. The complexes were used to catalyze the random copolymerization of ethylene with acrylates or methacrylates. 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subjects Applied sciences
Copolymerization
copper catalysts
Exact sciences and technology
metal-organic catalysts/organometallic catalysts
Organic polymers
Physicochemistry of polymers
polyacrylates
polyethylene (PE)
Preparation, kinetics, thermodynamics, mechanism and catalysts
title Fluorinated and ring-substituted bisbenzimidazole copper complexes for ethylene/acrylate copolymerization
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