A new family of zirconocene complexes of the type (Ind)ZrX (where Ind = CMeH and R = Me, Et and Ph) have been synthesised and fully characterised. Six new crystal structures have been reported (-(Ind)ZrBr, -(Ind)ZrCl, -(Ind)Zr(CHPh), -(Ind)Zr(CHPh), -(Ind)ZrBr and -(Ind)Zr(CHPh)). The complexes were studied for slurry-phase ethylene polymerisation when immobilised on solid polymethylaluminoxane (sMAO). Variation in the initiation group was found to have greater influence over polymerisation activity for -catalysts than -catalysts, with -alkyl catalysts showing higher polymerisation activities than -halide. Below 70 °C, polymerisation activity follows the order sMAO--(Ind)Zr(CHPh) sMAO--(Ind)ZrCl and sMAO--(Ind)ZrBr (activities of 657, 561, and 452 kg mol h bar, respectively). sMAO--(Ind)ZrBr produces HDPE with the highest molecular weight, followed by sMAO--(Ind)ZrCl and sMAO--(Ind)Zr(CHPh) ( of 503, 406, and 345 kg mol, respectively, at 50 °C). sMAO--(Ind)ZrBr produced HDPE with almost identical molecular weights to sMAO--(Ind)ZrCl (395 kg mol at 50 °C).
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http://dx.doi.org/10.1039/d1ra01912k | DOI Listing |
Dalton Trans
December 2024
Leibniz Institute for Catalysis, Albert-Einstein-Str. 29a, 18059 Rostock, Germany.
Starting from the alkyne complex CpZr(py)(η-MeSiCSiMe) (Cp = η-cyclopentadienyl, py = pyridine), the synthesis and complete characterisation of a zirconocene(IV) triazenido hydride complex and its use in the activation of small molecules is reported. The reaction with CO led to the formation of a zirconocene(IV) triazenido-formate complex, which was further investigated for its stability towards different bases with respect to the formation of formic acid. The experimentally observed reaction pathway was investigated computationally using DFT methods, revealing the favourable role of pyridine coordination in the hydrogen transfer from the triazene to the alkyne unit of the zirconocene reagent.
View Article and Find Full Text PDFRSC Adv
October 2024
State Key Laboratory of Biochemical Engineering, Key Laboratory of Biopharmaceutical Preparation and Delivery, Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences Beijing 100190 China
Polymer-derived ceramics (PDCs) have risen to prominence for applications in electrochemical energy storage, electromagnetic absorbing, and sensing materials, among others. However, a multitude of critical properties in PDCs are still limited by their intrinsic poor electrical conductivity. Herein, novel vinyl and zirconium-modified polycarbosilane precursors with improved electrical conductivity were synthesized through a Grignard coupling reaction of vinyl magnesium chloride and zirconocene dichloride, followed by the insertion polymerization with dichlorodimethylsilane and sodium.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2024
Wacker-Lehrstuhl für Makromolekulare Chemie Catalysis Research Center, Technische Universität München TUM School of Natural Sciences, Lichtenbergstraße 4, 85748, Garching Garching bei München, Germany.
The synthesis of group IV metallocene precatalysts for the polymerization of propylene generally yields two different isomers: The racemic isomer that produces isotactic polypropylene (iPP) and the meso isomer that produces atactic polypropylene (aPP). Due to its poor physical properties, aPP has very limited applications. To avoid obtaining blends of both polymers and thus diminish the mechanical and thermal properties of iPP, the meso metallocene complexes need to be separated from the racemic ones tediously-rendering the metallocene-based polymerization of propylene industrially far less attractive than the Ziegler/Natta process.
View Article and Find Full Text PDFChemistry
September 2024
Leibniz-Institut für Katalyse (LIKAT), Albert-Einstein-Str. 29a, 18059, Rostock, Germany.
Biradicals are important intermediates in the formation and breaking of a chemical bond. Their use as molecular switches is of particular interest. Much less is known about tetraradicals, which can, for example, consist of two biradical(oid) units.
View Article and Find Full Text PDFChem Sci
June 2024
CEMES, Université de Toulouse, CNRS 29 Rue Marvig 31055 Toulouse France
While hexaphenylsilacyclopentadiene (hexaphenylsilole) is viewed as an archetypal Aggregation-Induced Emission (AIE) luminogen, its isostructural hydrocarbon surrogate hexaphenylcyclopentadiene has strikingly never been investigated in this context, most probably due to a lack of synthetic availability. Herein, we report a straightforward synthesis of hexaphenylcyclopentadiene, the direct perarylation of cyclopentadiene upon copper(i) catalysis under microwave activation, with the formation of six new C-C bonds in a single synthetic operation. Using zirconocene dichloride as a convenient source of cyclopentadiene and a variety of aryl iodides as coupling partners, this copper-catalysed cross-coupling reaction gave rise to a series of unprecedented hexaarylcyclopentadienes.
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