Method for the production of a catalyst system for the...

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Polymers from only ethylenic monomers or processes of...

Reexamination Certificate

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C526S169100, C526S134000, C526S172000, C502S104000, C502S107000, C502S114000, C502S115000, C502S117000, C502S129000, C502S155000, C502S167000

Reexamination Certificate

active

06812305

ABSTRACT:

BACKGROUND OF THE INVENTION
The present invention relates to a process for preparing a catalyst system for the polymerization of olefins, which comprises initially charging one or more compounds of the formula I a or I b,
where the variables are defined as follows:
M is a transition metal of groups 5 to 10 of the Periodic Table of the Elements,
A is selected from among N, P and As,
A′ is selected from among O and S,
Nu
1
, Nu
2
are N or P,
X
1
, X
2
are halogen or C
1
-C
4
-alkoxy;
R
1
, R
2
are unsubstituted or substituted C
1
-C
12
-alkyl, C
3
-C
12
-cycloalkyl, C
7
-C
15
-aralkyl, C
6
-C
14
-aryl or five- or six-membered N-containing heteroaryl,
R
3
, R
4
are hydrogen, unsubstituted or substituted C
1
-C
12
-alkyl, C
3
-C
12
-cycloalkyl, C
7
-C
15
-aralkyl, C
6
-C
14
-aryl or five- or six-membered N-containing heteroaryl,
R
5
to R
7
are each selected independently from among hydrogen, unsubstituted or substituted C
1
-C
12
-alkyl, C
3
-C
12
-cycloalkyl, C
7
-C
15
-aralkyl, C
6
-C
14
-aryl and five- and six-membered N-containing heteroaryl, halogen, C
1
-C
6
-alkoxy, NO
2
, SiR
8
R
9
R
10
and OSiR
8
R
9
R
10
where adjacent radicals together with the parent heteroaryl may form a 5- to 10-membered ring,
R
8
to R
10
are selected independently from among hydrogen and substituted or unsubstituted C
1
-C
12
-alkyl, C
3
-C
12
-cycloalkyl, C
7
-C
15
-aralkyl and C
6
-C
14
-aryl; then adding a molecularly defined activator of the formulae II a to c
[(L—H)]
+
[(M′)Q
1
Q
2
Q
3
Q
4
]

  II a
 [(CAr
3
)]
+
[(M′)Q
1
Q
2
Q
3
Q
4
]

  II b
[(M′)Q
1
Q
2
Q
3
]  II c
where the radicals have the following meanings:
[L—H]
+
is a Brønsted acid, where L is an electron-neutral Lewis base,
M′ is an element of group 13 of the Periodic Table of the elements,
Q
1
to Q
4
are selected independently from among hydride, unsubstituted or substituted C
1
-C
12
-alkyl, C
3
-C
12
-cycloalkyl, C
7
-C
15
-aralkyl, C
6
-C
14
-aryl and halide, with the proviso that not more than two radicals Q
1
and Q
2
are halide;
Ar are identical or different and are selected from among unsubstituted or substituted C
6
-C
14
-aryl,
and finally adding an alkylating agent selected from among LiR
11
, MgR
11
R
12
and AlR
12
R
13
R
14
, where
R
11
to R
14
are selected independently from among unsubstituted or substituted C
1
-C
12
-alkyl, C
3
-C
12
-cycloalkyl, C
7
-C
15
-aralkyl and C
6
-C
14
-aryl.
The present invention also provides the catalyst system prepared by the abovementioned process and provides a process for the polymerization and copolymerization of olefins using this catalyst system.


REFERENCES:
patent: 0 277 004 (1988-08-01), None
patent: 0 468 537 (1992-01-01), None
patent: 0 561 479 (1993-09-01), None
patent: 96/23010 (1996-08-01), None
patent: 98/27124 (1998-06-01), None
patent: WO98/27124 (1998-06-01), None
patent: 98/30612 (1998-07-01), None
patent: WO99/12981 (1999-03-01), None
patent: 99/12981 (1999-03-01), None
Hans-Herbert Brintzinger et al.: “Stereospezifische olfinpolymerisation mit chiralen metalloceakatalysatoren” Angew. Chem., vol. 107, pp. 1255-1283.
George J.P. Britovsek et al.: “Iron and cobalt ethylene polymerization catalysts bearing 2,6-bis(imino)pyridyl ligands: synthesis, structures, and polymerization studies” J. Am. Chem., vol. 121, pp. 8728-8740 1999.
George J.P. Britovsek et al.: “Novel olefin polymerization catalysts based on iron and cobalt” Chem. Commun., pp. 849-850 1998.
Brooke L. Small et al.: “Highly active iron and cobalt catalysts for the polymerization of ethylene” J. Am. Chem. Soc., vol. 120, pp. 4049-4050 1998.
X. Yang et al.: “Cation-like' homogenous olefin polymerization catalysts based upon zirconocene alkyls and tris(pentafluorophenyl)borane” J. Am. Chem., vol. 113, No. 9, pp. 3623-3625 1991.

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