TY - JOUR
T1 - Novel high and ultrahigh molecular weight poly(propylene) plastomers by asymmetric hafnocene catalysts
AU - Cobzaru, Cecilia
AU - Deisenhofer, Sandra
AU - Harley, Andrew
AU - Troll, Carsten
AU - Hild, Sabine
AU - Rieger, Bernhard
PY - 2005/6/16
Y1 - 2005/6/16
N2 - The novel asymmetric ansa-complexes [1-(9-η5-fluorenyl)-2- (2,5,7-trimethyl-indenyl)ethane]hafnium dichloride (7a) and [1-(9- η5-fluorenyl)-2-(2,4,6-trimethyl-indenyl)ethane]hafnium dichloride (7b) were prepared and used as catalysts for propylene homopolymerization reactions after in situ activation. The synthetic route allows to separate the 4,6- and 5,7-substituted ligand isomers before the complexation step. The orientation of the methyl groups to the "front" (4,6) or to the "back" (5,7) of the tetrahedral hafnocene dichloride species influences their performances in polymerization reactions. Whereas hafnocene (7b) which bears trimethyl substitution at 2,4,6-positions of the indenyl moiety exhibits only moderate activity, the 2,5,7-trimethyl substituted structure (7a) produces isotactic poly(propylene)s with high molecular weights (up to M̄w = 9.0 × 105 g · mol -1) and high activities [up to 3.2 × 105 kg of PP (mol Hf × h)-1]. A comparative analysis of polymerization data and mechanical behavior of 7a, and previously reported 6,7-indenyl substituted complex 6b are reported.
AB - The novel asymmetric ansa-complexes [1-(9-η5-fluorenyl)-2- (2,5,7-trimethyl-indenyl)ethane]hafnium dichloride (7a) and [1-(9- η5-fluorenyl)-2-(2,4,6-trimethyl-indenyl)ethane]hafnium dichloride (7b) were prepared and used as catalysts for propylene homopolymerization reactions after in situ activation. The synthetic route allows to separate the 4,6- and 5,7-substituted ligand isomers before the complexation step. The orientation of the methyl groups to the "front" (4,6) or to the "back" (5,7) of the tetrahedral hafnocene dichloride species influences their performances in polymerization reactions. Whereas hafnocene (7b) which bears trimethyl substitution at 2,4,6-positions of the indenyl moiety exhibits only moderate activity, the 2,5,7-trimethyl substituted structure (7a) produces isotactic poly(propylene)s with high molecular weights (up to M̄w = 9.0 × 105 g · mol -1) and high activities [up to 3.2 × 105 kg of PP (mol Hf × h)-1]. A comparative analysis of polymerization data and mechanical behavior of 7a, and previously reported 6,7-indenyl substituted complex 6b are reported.
KW - Asymmetric metallocenes
KW - Hafnium catalysts
KW - Plastomers
KW - Poly(propylene) (PP)
KW - Propylene
UR - http://www.scopus.com/inward/record.url?scp=21244471890&partnerID=8YFLogxK
U2 - 10.1002/macp.200400551
DO - 10.1002/macp.200400551
M3 - Article
AN - SCOPUS:21244471890
SN - 1022-1352
VL - 206
SP - 1231
EP - 1240
JO - Macromolecular Chemistry and Physics
JF - Macromolecular Chemistry and Physics
IS - 12
ER -