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The objectives of this work were to address the fundamental characteristics of ansa-zirconocene catalyzed E/diene copolymerization and E/diene/1-hexene and E/diene/propylene terpolymerizations, and the quantitative relationship between diene structure and polymer chain propagation rate constant in term of quantifiable catalytic active sites. One of the most important but unknown factors in olefins ansa-zirconocene complexes is the distribution of the catalyst between sites actively participating in polymer chain formation and dormant sites. A set of ethylene/dienes copolymerizations, and ethylene/dienes/1-hexene and ethylene/dienes/1-hexene terpolymerizations catalyzed with -zirconocenes/borate/triisobutylaluminium (-Et(Ind)ZrCl/[PhC][B(CF)]/triisobutylaluminium (TIBA) were performed in toluene at 50 °C To determine the active center [C*]/[Zr] ratio variation in the copolymerization of E with different dienes and their terpolymerization with 1-hexene and propylene, each polymer propagation chain ends were quenched with 2-thiophenecarbonyl, which selectively quenches the metal-polymer bonds through acyl chloride. The ethylene, propylene, 1-hexene, and diene composition-based propagation rate constants (E, P, 1-H, and diene), thermal (melting and crystalline) properties, composition (mol% of ethylene, propylene, 1-hexene, and diene), molecular weight, and polydispersity were also studied in this work. Systematic comparisons of the proportion of catalytically [Zr]/[C*] active sites and polymerization rate constant () for -zirconocenes catalyzed E/diene, E/diene/1-hexene, and E/diene/propylene polymerization have not been reported before. We evaluated the addition of 1-hexene and propylene as termonomers in the copolymerization with E/diene. To make a comparison for each diene under identical conditions, we started the polymerization by introducing an 80/20 mole ratio of E/P and 0.12 mol/L of 1-hexene in the system. The catalyst behavior against different dienes, 1-hexene, and propylene is very interesting, including changes in thermal properties, cyclization of 1-hexene, and decreased incorporation of isoprene and butadiene, changes in the diffusion barriers in the system, and its effect on .
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http://dx.doi.org/10.3390/polym14163239 | DOI Listing |
Polymers (Basel)
November 2023
Institut de Química Computacional i Catàlisi and Departament de Química, Universitat de Girona, c/ Maria Aurèlia Capmany 69, 17003 Girona, Spain.
The aim of this work is to investigate the influence of the ethanol content of adducts on the catalytic behavior of related Ziegler-Natta (ZN) catalysts in propylene homo- and copolymerizations (with 1-hexene comonomer) in terms of activity, isotacticity, H response, and comonomer incorporation. For this purpose, three MgCl.nEtOH adducts with n values of 0.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2023
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, North Zhongshan Rd. 3663, 200062, Shanghai, China.
Selective conversion of syngas to value-added olefins has attracted considerable research interest. Regulating product distribution remains challenging, such as achieving higher olefin selectivity, propylene/ethylene (P/E) and olefin/paraffin (O/P) ratios. A new pentasil zeolite Al-IDM-1 with recently approved -ION structure, composed of 17-membered-ring (MR) extra-large lobed pores and intersected 10-MR medium pores, shows a C selectivity up to 85 % and a high O/P value of 14 in the conversion of syngas when being combined with Zn Al O oxide.
View Article and Find Full Text PDFACS Omega
September 2022
Research School of Polymeric Materials, School of Materials Science & Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
Terpolymerizations of newly synthesized ethylene (E), vinylcyclohexene (VCH), and 1-hexene were carried out with symmetrical metallocene catalysts -MeSi(2-Me-4-Ph-Ind)ZrCl (catalyst A) and -Et(Ind)ZrCl (catalyst B). X-ray diffractometry (XRD), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), high-temperature gel permeation chromatography (GPC), and nuclear magnetic resonance (NMR) spectroscopy were used to evaluate the behavior and microstructure of the polymers. The activity of catalyst B was 1.
View Article and Find Full Text PDFPolymers (Basel)
August 2022
Research School of Polymeric Materials, School of Materials Science & Engineering, Jiangsu University, Zhenjiang 212013, China.
The objectives of this work were to address the fundamental characteristics of ansa-zirconocene catalyzed E/diene copolymerization and E/diene/1-hexene and E/diene/propylene terpolymerizations, and the quantitative relationship between diene structure and polymer chain propagation rate constant in term of quantifiable catalytic active sites. One of the most important but unknown factors in olefins ansa-zirconocene complexes is the distribution of the catalyst between sites actively participating in polymer chain formation and dormant sites. A set of ethylene/dienes copolymerizations, and ethylene/dienes/1-hexene and ethylene/dienes/1-hexene terpolymerizations catalyzed with -zirconocenes/borate/triisobutylaluminium (-Et(Ind)ZrCl/[PhC][B(CF)]/triisobutylaluminium (TIBA) were performed in toluene at 50 °C To determine the active center [C*]/[Zr] ratio variation in the copolymerization of E with different dienes and their terpolymerization with 1-hexene and propylene, each polymer propagation chain ends were quenched with 2-thiophenecarbonyl, which selectively quenches the metal-polymer bonds through acyl chloride.
View Article and Find Full Text PDFInorg Chem
May 2022
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. China.
A series of new zirconium complexes bearing bulkier amine bis(phenolate) tetradentate ligands, MeNCHCHN{CH(2-O-3-R-5-Bu-CH)}ZrCl [R = CPhMe (); CMePh (); CPh (); Ph (); 3,5-MeCH (); 3,5-BuCH (); 4-BuCH ()], were synthesized and characterized by H nuclear magnetic resonance (NMR), C NMR, and elemental analyses. The molecular structures of complexes and were determined by single-crystal X-ray diffraction analysis. The X-ray crystallography analysis reveals that these complexes display a slightly distorted octahedral geometry around their metal centers.
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