The syntheses, structures and olefin polymerization behavior of Ti complexes containing a pair of chelating aminotropone [ON] ligands are reported. DFT studies revealed that bis(aminotropone) Ti complexes, when activated, provide a metal alkyl in the cis position to a vacant coordination site for monomer binding, suggesting great potential for the polymerization of olefinic monomers. Unlike Ti‐FI catalysts, bis(aminotropone) Ti complexes do not require the presence of steric bulk in close proximity to the anionic donor. Bis(aminotropone) Ti complexes combined with MAO display high ethylene polymerization activities (max. 27 200 kg polymer per mol catalyst and hour) comparable to those obtained with early group‐four metallocene catalysts under identical conditions.
The new photocatalysts were synthesized with inorganic clusters of polyoxometalats (POMs) and graphitic carbon nitride (g-C3N4) under hydrothermal conditions. In this research, for the first time, the preyssler-type of polyoxometalate...
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