Metallocene compositions

Catalyst – solid sorbent – or support therefor: product or process – Catalyst or precursor therefor – Plural component system comprising a - group i to iv metal...

Reexamination Certificate

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C502S117000, C502S152000, C502S155000, C526S160000, C526S943000

Reexamination Certificate

active

06380123

ABSTRACT:

FIELD
This invention relates to metallocene compositions and their use in the preparation of catalyst systems for olefin polymerization, particularly propylene polymerization.
BACKGROUND
The use of metallocene compositions in olefin polymerization is well known. Metallocenes containing substituted, bridged indenyl derivatives are noted for their ability to produce isotactic propylene polymers having high isotacticity and narrow molecular weight distribution. Considerable effort has been made toward obtaining metallocene produced propylene polymers having ever-higher molecular weight and melting point, while maintaining suitable catalyst activity.
Toward this end it has been found that there is a direct relationship between the way in which a metallocene is substituted, and the molecular structure of the resulting polymer. For the substituted, bridged indenyl type metallocenes, it is now well established that the type and arrangement of substituents on the indenyl groups, as well as the type of bridge connecting the indenyl groups, determines such polymer attributes as molecular weight and melting point. Unfortunately, it is impossible at this time to accurately correlate specific substitution or bridging patterns with specific polymer attributes, though trends may be identified.
For example, U.S. Pat. No. 5,840,644 describes certain metallocenes containing aryl-substituted indenyl derivatives as ligands, which are said to provide propylene polymers having high isotacticity, narrow molecular weight distribution and very high molecular weight.
Likewise, U.S. Pat. No. 5,936,053 describes certain metallocene compounds said to be useful for producing high molecular weight propylene polymers. These metallocenes have a.specific hydrocarbon substituent at the 2 position and an unsubstituted aryl substituent at the 4 position, on each indenyl group of the metallocene compound.
WO 98/40419 and WO 99/42497 both describe certain supported catalyst systems for producing propylene polymers having high melting point. Metallocene compositions and their activators are often combined with a support material in order to obtain a catalyst system that is less likely to cause reactor fouling. However, it is known that supported metallocene catalyst systems tend to result in a polymer having lower melting point than would otherwise be obtained if the metallocene were not supported.
Much of the current research in this area has been directed toward using metallocene catalyst systems under commercially relevant process conditions, to obtain propylene polymers having melting points higher than known metallocene catalyst systems and close to, or as high as, propylene polymers obtained using conventional, Ziegler-Natta catalyst systems, i.e., 160° C. or higher. The present inventors have discovered metallocene compounds that have this capability.
SUMMARY
The present invention relates generally to metallocene compounds represented by the formula:
wherein:
M is a metal of Group 4, 5, or 6 of the Periodic Table preferably, zirconium, hafnium and titanium, most preferably zirconium;
R
1
and R
2
are identical or different, preferably identical, and are one of a hydrogen atom, a C
1
-C
10
alkyl group, preferably a C
1
-C
3
alkyl group, a C
1
-C
10
alkoxy group, preferably a C
1
-C
3
alkoxy group, a C
6
-C
10
aryl group, preferably a C
6
-C
8
aryl group, a C
6
-C
10
aryloxy group, preferably a C
6
-C
8
aryloxy group, a C
2
-C
10
alkenyl group, preferably a C
2
-C
4
alkenyl group, a C
7
-C
40
arylalkyl group, preferably a C
7
-C
10
arylalkyl group, a C
7
-C
40
alkylaryl group, preferably a C
7-C
12
alkylaryl group, a C
8
-C
40
arylalkenyl group, preferably a C
8
-C
12
arylalkenyl group, or a halogen atom, preferably chlorine; or a conjugated diene which is optionally substituted with one or more hydrocarbyl, tri(hydrocarbyl)silyl groups or hydrocarbyl, tri(hydrocarbyl)silylhydrocarbyl groups, said diene having up to 30 atoms not counting hydrogen;
R
5
and R
6
are identical or different, preferably identical, are one of a hydrogen atom, a halogen atom, preferably a fluorine, chlorine or bromine atom, a C
1
-C
10
alkyl group, preferably a C
1
-C
4
alkyl group, which may be halogenated, a C
6
-C
10
aryl group, which may be halogenated, preferably a C
6
-C
8
aryl group, a C
2
-C
10
alkenyl group, preferably a C
2
-C
4
alkenyl group, a C
7
-C
40
arylalkyl group, preferably a C
7
-C
10
arylalkyl group, a C
7
-C
40
alkylaryl group, preferably a C
7
-C
12
alkylaryl group, a C
8
-C
40
arylalkenyl group, preferably a C
8
-C
12
arylalkenyl group, a —NR
2
15
, —SR
15
, —OR
15
, —OSiR
3
15
or —PR
2
15
radical, wherein: R
15
is one of a halogen atom, preferably a chlorine atom, a C
1
-C
10
alkyl group, preferably a C
1
-C
3
alkyl group, or a C
6
-C
10
aryl group, preferably a C
6
-C
9
aryl group;
R
7
is
 wherein:
R
17
to R
24
are as defined for R
1
and R
2
, or two or more adjacent radicals R
17
to R
24
, including R
20
and R
21
, together with the atoms connecting them form one or more rings;
M
2
is carbon, silicon, germanium or tin;
the radicals R
3
, R
4
, and R
10
are identical or different and have the meanings stated for R
5
and R
6
, or two adjacent R
10
radicals are joined together to form a ring, preferably a ring containing from about 4-6 carbon atoms.
More specifically, the present invention relates generally to metallocene compounds represented by the formula:
wherein:
M
1
is selected from the group consisting of titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum and tungsten;
R
1
and R
2
are identical or different, and are one of a hydrogen atom, a C
1
-C
10
alkyl group, a C
1
-C
10
alkoxy group, a C
6
-C
10
aryl group, a C
6
-C
10
aryloxy group, a C
2
-C
10
alkenyl group, a C
2
-C
40
alkenyl group, a C
7
-C
40
arylalkyl group, a C
7
-C
40
alkylaryl group, a C
8
-C
40
arylalkenyl group, an OH group or a halogen atom; or a conjugated diene which is optionally substituted with one or more hydrocarbyl, tri(hydrocarbyl)silyl groups or hydrocarbyl, tri(hydrocarbyl)silylhydrocarbyl groups, said diene having up to 30 atoms not counting hydrogen;
R
3
are identical or different and are each a hydrogen atom, a halogen atom, a C
1
-C
10
alkyl group which may be halogenated, a C
6
-C
10
aryl group which may be halogenated, a C
2
-C
10
alkenyl group, a C
7
-C
40
-arylalkyl group, a C
7
-C
40
alkylaryl group, a C
8-C
40
arylalkenyl group, a —NR′
2
, —SR′, —OR′, —OSiR′
3
or —PR′
2
radical, wherein: R′ is one of a halogen atom, a C
1
-C
10
alkyl group, or a C
6
-C
10
aryl group;
R
4
to R
7
are identical or different and are hydrogen, as defined for R
3
or two or more adjacent radicals R
5
to R
7
together with the atoms connecting them form one or more rings;
R
13
is represented by the formula:
 wherein:
R
17
to R
24
are as defined for R
1
and R
2
, or two or more adjacent radicals R
17
to R
24
, including R
20
and R
21
, together with the atoms connecting them form one or more rings;
M
2
is carbon, silicon, germanium or tin;
R
8
, R
9
, R
10
R
11
and R
12
are identical or different and have the meanings stated for R
4
to R
7
.
The present invention further relates to metallocene catalyst systems comprising one or more or the above compounds and one or more activators or cocatalysts, and optionally, support material, and to the use of such metallocene catalyst systems in olefin polymerization, particularly propylene polymer polymerization.
DESCRIPTION
In one embodiment, the metallocenes of the present invention may be represented by the formula:
wherein:
M is a metal of Group 4, 5, or 6 of the Periodic Table preferably, zirconium, hafnium and titanium, most preferably zirconium;
R
1
and R
2
are identical or different, preferably identical, and are one of a hydrogen atom, a C
1
-C
10
alkyl group, preferably a C
1
-C
3
alkyl group, a C
1
-C
10
alkoxy group, preferably a C
1
-C
3
alkoxy group, a C
6
-C
10
aryl group, preferably a C
6
-C
8
aryl group, a C
6
-C

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