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Abstract
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Ethylene polymerization was carried out by using a group of new dizirconium(IV) tetrapyrrole complexes as catalysts and MAO as co-catalyst under 1 atmosphere pressure of ethylene gas at 25 and 40C. The highest value of catalyst activity was obtained at 40C by using bizirconium complexes including one calix[4]pyrrole between two zirconium centers and two terminal chlorines, while zirconium(IV) complexes with coordinated THF, almost have not catalytic activity. The maximum catalytic activity mounted to 830 kg=mol bar h by Zr2 (Cy4Pyr4)Cl4. The results show that the structure of the coordination sphere of zirconium(IV) has great influence on the rate of polymerization, molar masses of forming polymer, and its molecular mass distribution.
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