TY - JOUR
T1 - High molecular weight atactic polypropylene prepared by zirconium complexes of an amine bis(phenolate) ligand
AU - Groysman, Stanislav
AU - Tshuva, Edit Y.
AU - Reshef, Dvora
AU - Gendler, Shimrit
AU - Goldberg, Israel
AU - Kol, Moshe
AU - Goldschmidt, Zeev
AU - Shuster, Michael
AU - Lidor, Gershon
PY - 2002
Y1 - 2002
N2 - The polymerization of propylene employing the recently developed amine bis(phenolate) zirconium catalysts is reported for the first time. The polymerizations were conducted in liquid propylene employing two different experimental setups, and two different precatalysts, based on the same amine bis(phenolate) ligand having a dimethylamino donor on a sidearm. The first precatalyst studied was a dibenzyl zirconium complex, which was found to lead to high molecular weight atactic polypropylene. The effects of the cocatalyst, the ratio between the cocatalyst and the precatalyst, and the polymerization temperature on the nature of the resulting polymer and the activity of the catalyst were studied. Reducing the relative amount of the cocatalyst and lowering the polymerization temperature increased the molecular weight of the polymer, and a temperature of 50°C led to the most active catalyst. A dichloro zirconium complex of the same ligand, expected to show a higher hydrolytic and thermal stability was developed, its X-ray structure was solved, and its activity in polymerization of propylene was studied and found to be similar to that of the dibenzyl precatalyst.
AB - The polymerization of propylene employing the recently developed amine bis(phenolate) zirconium catalysts is reported for the first time. The polymerizations were conducted in liquid propylene employing two different experimental setups, and two different precatalysts, based on the same amine bis(phenolate) ligand having a dimethylamino donor on a sidearm. The first precatalyst studied was a dibenzyl zirconium complex, which was found to lead to high molecular weight atactic polypropylene. The effects of the cocatalyst, the ratio between the cocatalyst and the precatalyst, and the polymerization temperature on the nature of the resulting polymer and the activity of the catalyst were studied. Reducing the relative amount of the cocatalyst and lowering the polymerization temperature increased the molecular weight of the polymer, and a temperature of 50°C led to the most active catalyst. A dichloro zirconium complex of the same ligand, expected to show a higher hydrolytic and thermal stability was developed, its X-ray structure was solved, and its activity in polymerization of propylene was studied and found to be similar to that of the dibenzyl precatalyst.
UR - http://www.scopus.com/inward/record.url?scp=0042131524&partnerID=8YFLogxK
U2 - 10.1560/bbtt-m841-mddw-1g3l
DO - 10.1560/bbtt-m841-mddw-1g3l
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AN - SCOPUS:0042131524
SN - 0021-2148
VL - 42
SP - 373
EP - 381
JO - Israel Journal of Chemistry
JF - Israel Journal of Chemistry
IS - 4
ER -