Metallocenes with silyl-substituted bridges and their use for ol

Catalyst – solid sorbent – or support therefor: product or process – Catalyst or precursor therefor – Organic compound containing

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502152, 526127, 526160, 526351, 526352, 526943, 526 12, 526 43, 526 53, C08F 464

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059453672

DESCRIPTION:

BRIEF SUMMARY
BACKGROUND OF THE INVENTION

1. Field of Invention
The invention relates to new metallocenes and their use as catalysts in olefin polymerization.
2. Prior Art
Metallocenes of the metals of transition group IV of the Periodic Table of the Elements are highly active catalysts for the polymerization of olefins. The resulting polyolefins have new property combinations and supplement the product range of the polyolefins prepared hitherto using known conventional Ziegler-Natta catalysts.
It is known that catalysts based on unbridged, substituted and unsubstituted biscyclopentadienyl metallocenes in combination with aluminoxanes as cocatalyst can be used for the preparation of polyethylene and ethyleneolefin copolymers (EXXON EPA 128 046).
It is also known that stereoregular polyolefins can be prepared using bridged, chiral metallocenes. For bridging the ligand systems, use is mostly made of dimethylsilanediyl groups (CHISSO EPA 316 155), methylphenylsilanediyl groups (HOECHST EPA 320 762), ethylene groups (Brintzinger et al., J. Organomet. Chem., 288 (1985) 63-67) and isopropylidene bridges (Mitsui Toatsu EPA 459 264). Depending on the ligand type and the substituents, isotactic, syndiotactic, hemiisotactic, stereoblock-type and atactic homopolymers and copolymers having aliphatic or cyclic structures can be prepared.
As ligands, preference is given to using substituted and unsubstituted cyclopentadienyl units (CHISSO EPA 316 155), substituted and unsubstituted indenyl units (Hoechst EPA 302 424; Hoechst EPA 485 823) and also substituted and unsubstituted cyclopentadienyl units in combination with unsubstituted fluorenyl groups (Mitsui Toatsu EPA 412 416).
Likewise, it is known that bridged metallocenes having a cyclopentadienyl system and a heteroatom ligand (constrained geometry catalyst) can also be used for the polymerization of olefins (EXXON U.S. Pat. No. 5,096,867).
Among these various types of metallocene, the bridged, chiral, substituted bisindenyl systems have attained particular importance. Thus, it was able to be shown that the type of substituents and the position of the substituents on the ligand of the metallocene have a significant influence on the reactivity of the catalyst system and the stereoregular structure of the polyolefins obtained. Two possible substitution patterns in particular have been found to be advantageous. The first possibility entails substitution of the indenyl ligand in the 2, 4 and/or 6 position (Hoechst EPA 485823; Angew. Chem., 10 (1992) 1373) while the second possibility is fusion onto the benzene ring of the indenyl ligand (Organometallics 1994, 13, 964-970). Both types of catalyst can be used for preparing isotactic polypropylene and ethylene-.alpha.-olefin copolymers.
Multiply substituted indenyl ligands can be prepared only at considerable expense. Relatively simple systems having good activity and containing products, in particular polypropylene, having relatively low molar masses which are too low for many applications and represent the lower limit for industrial use.
It is therefore an object of the invention to find further structural variants of bridged metallocenes as catalysts for the polymerization of olefins which give polyolefins, in particular polypropylene, having relatively high molar masses.


BRIEF SUMMARY OF THE INVENTION

It has now surprisingly been found that silyl-substituted, diyl-bridged metallocene systems are suitable catalysts for the preparation of polyolefins and in particular of polypropylenes having relatively high molar masses.
The present invention accordingly provides metallocenes of the formula I ##STR2## where M is a metal selected from the group consisting of Ti, Zr, Hf, V, Nb and Ta or an element selected from the group consisting of the lanthanides, -C.sub.10 -alkyl group, a C.sub.1 -C.sub.10 -alkoxy group, a C.sub.6 -C.sub.10 -aryl group, a C.sub.6 -C.sub.10 -aryloxy group, a C.sub.2 -C.sub.10 -alkenyl group, a C.sub.7 -C.sub.20 -arylalkyl group, a C.sub.7 -C.sub.20 -alkylaryl group, a C.sub.8 -C.sub.20 -aryl-alkenyl group, hydro

REFERENCES:
patent: 5541350 (1996-07-01), Murata et al.
patent: 5767209 (1998-06-01), McNally

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