E = O (1d)) has been prepared by the reaction of corresponding phenol derivatives with Cp*TiCl3 in the presence of excessive triethylamine. Under the conditions of low Al/Ti molar ratio (e.g. 500) and high reaction temperatures (≥ 70οC)
all the titanium complexes display higher catalytic activities towards the syndiospecific polymerization of styrene
in the presence of modified methylaluminoxane (MMAO) as a cocatalyst
than their mother complex Cp*TiCl3. The catalyst activities and polymer yields as well as polymer properties are considerably affected by the steric and electronical effects of the bidentate ligands.
Abstract
A series of titanium complexes Ar[O
E]Cp*TiCl (Cp* = C5Me5
Ar = 1
2-phenylene
E = NH (1a); Ar = 1
2-phenylene
E = O (1b); Ar = 2
2′-diphenylene
E = O (1c); Ar = 2
2′-dinaphthalene
E = O (1d)) has been prepared by the reaction of corresponding phenol derivatives with Cp*TiCl3 in the presence of excessive triethylamine. Under the conditions of low Al/Ti molar ratio (e.g. 500) and high reaction temperatures (≥ 70οC)
all the titanium complexes display higher catalytic activities towards the syndiospecific polymerization of styrene
in the presence of modified methylaluminoxane (MMAO) as a cocatalyst
than their mother complex Cp*TiCl3. The catalyst activities and polymer yields as well as polymer properties are considerably affected by the steric and electronical effects of the bidentate ligands.
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