The behavior in propylene polymerization of divalent titanium compounds of type [η6-areneTiAl2Cl8], both as such and supported on activated MgCl2, has been studied and compared to that of the simple catalyst MgCl2/TiCl4. Triethylaluminium was used as cocatalyst. The Ti-arene complexes were active both in the presence and in the absence of hydrogen, in contrast to earlier reports that divalent titanium species are active for ethylene but not for propylene polymerization. 13C-NMR analysis of low molecular weight polymer fractions indicated that the hydrogen activation effect observed for the MgCl2-supported catalysts should be ascribed to reactivation of 2,1-inserted ("dormant") sites via chain transfer, rather than to (re)generation of active trivalent Ti via oxidative addition of hydrogen to divalent species. Decay in activity during polymerization was observed with both catalysts, indicating that for MgCl2/ TiCl4 catalysts decay is not necessarily due to overreduction of Ti to the div...
Propylene polymerization with catalysts containing divalent titanium
MALDOTTI, Andrea
1997
Abstract
The behavior in propylene polymerization of divalent titanium compounds of type [η6-areneTiAl2Cl8], both as such and supported on activated MgCl2, has been studied and compared to that of the simple catalyst MgCl2/TiCl4. Triethylaluminium was used as cocatalyst. The Ti-arene complexes were active both in the presence and in the absence of hydrogen, in contrast to earlier reports that divalent titanium species are active for ethylene but not for propylene polymerization. 13C-NMR analysis of low molecular weight polymer fractions indicated that the hydrogen activation effect observed for the MgCl2-supported catalysts should be ascribed to reactivation of 2,1-inserted ("dormant") sites via chain transfer, rather than to (re)generation of active trivalent Ti via oxidative addition of hydrogen to divalent species. Decay in activity during polymerization was observed with both catalysts, indicating that for MgCl2/ TiCl4 catalysts decay is not necessarily due to overreduction of Ti to the div...I documenti in SFERA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.