Bis(2-R-ind)ZrCl2 (R: H or phenyl) was supported on different types of silica by in situ impregnation method and used for ethylene polymerization. In this method, the step of catalyst loading on support was eliminated and common alkyl aluminum (triisobutylaluminum, TiBA) cocatalyst was used instead of expensive methyl aluminiumoxane (MAO) cocatalyst in the polymerization. The effect of surface ...

bis(2-r-ind)zrcl2 (r: h or phenyl) was supported on different types of silica by in situ impregnation method and used for ethylene polymerization. in this method, the step of catalyst loading on support was eliminated and common alkyl aluminum (triisobutylaluminum, tiba) cocatalyst was used instead of expensive methyl aluminiumoxane (mao) cocatalyst in the polymerization. the effect of surface ...

Both metallocene and Phillips chromium catalysts are used in the commercial manufacture of polyethylene. Unlike most other systems, Chevron Chemical (CPC) platform does not use methylaluminoxane or fluoroorganic boranes. Instead, support itself serves to activate (ionize) metallocenes, which then polymerize ethylene at high activity. Most these solid acid supports can also be anchor Cr make a c...

In this study we have tested the ability of a standard DFT computational protocol to reproduce the experimentally obtained stereoselectivity of 26 different C2-symmetric zirconocene catalysts active in propylene polymerization. The catalysts were chosen for their relevance in metallocene catalyzed polymerization of propylene. To this end, primary insertion of both si- and re-propylene enantiofa...

We treated silica with tris(pentafluorophenyl)borane, B(C6F5)3, to create borane-functionalized support, SiO2–B(C6F5)3 which was then used as a support and co-catalyst for the in situ activated dichloro-zirconocene (Cp2ZrCl2/TIBA) and dimethyl-zirconocene catalyst systems (Cp2Zr(CH3)2) for ethylene polymerization. The surface modifications of SiO2– B(C6F5)3 was investigated by SEM–EDX, FTIR and...

In the last years huge efforts have been made to develop new activation modes in order to synthesize complex scaffolds in an enantiopure form. The most common approach has been the development of new catalysts to activate an “unreactive” compound A that will react with a highly reactive compound B to render C. However, recently a new approach pushes the boundaries of organic chemistry: synergis...