Preformed catalytic system comprising a rare-earth metallocene

Patent metadata

Field	Value
Publication number	US-10934377-B2
Application number	US-201716320014-A
Country	US
Kind code	B2
Filing date	Jul 24, 2017
Priority date	Jul 25, 2016
Publication date	Mar 2, 2021
Grant date	Mar 2, 2021

Abstract

A catalytic system based at least on a preformation monomer which is ethylene or a mixture of ethylene and of a conjugated diene, on a metallocene of formula {P(Cp1)(Cp2)Y} or Cp3Cp4Y and on an organometallic compound as cocatalyst, Y denoting a group comprising a metal atom which is a rare earth metal, the Cp1, Cp2, Cp3 and Cp4 groups, which are identical or different, being selected from the group consisting of fluorenyl groups, cyclopentadienyl groups and indenyl groups, the groups being substituted or unsubstituted, and P being a group bridging the two Cp1 and Cp2 groups and comprising a silicon or carbon atom, is provided. Such a catalytic system exhibits an improved stability of the catalytic activity over time, in particular on storage.

First claim

The invention claimed is:

1. A catalytic composition comprising at least:
a preformation monomer which is ethylene or a mixture of ethylene and of a conjugated diene,
an organometallic compound as cocatalyst, and
a metallocene of formula (Ia) or (Ib):
{P(Cp 1 )(Cp 2 )Y}  (Ia)

Cp 3 Cp 4 Y  (Ib)

Y denoting a group comprising Met-G, with Met denoting a rare earth metal and G denoting a group comprising the borohydride BH 4 unit or denoting a halogen atom X selected from the group consisting of chlorine, fluorine, bromine and iodine,
Cp 1 , Cp 2 , Cp 3 and Cp 4 , which are identical or different, being selected from the group consisting of fluorenyl groups, cyclopentadienyl groups and indenyl groups, the groups being substituted or unsubstituted, and
P being a group bridging the two Cp 1 and Cp 2 groups and comprising a silicon or carbon atom.

2. A catalytic composition according to claim 1 , wherein the cocatalyst is an organomagnesium compound.

3. A catalytic composition according to claim 1 , wherein the cocatalyst is an organometallic compound comprising an alkyl group bonded to the metal atom.

4. A catalytic composition according to claim 1 , wherein the cocatalyst is a dialkylmagnesium compound or an alkylmagnesium halide.

5. A catalytic composition according to claim 1 , in wherein Cp 1 and Cp 2 are identical and are selected from the group consisting of substituted fluorenyl groups and the unsubstituted fluorenyl group of formula C 13 H 8 .

6. A catalytic composition according to claim 1 , wherein Cp 1 and Cp 2 each represent an unsubstituted fluorenyl group of formula C 13 H 8 .

7. A catalytic composition according to claim 1 , wherein G denotes chlorine or the group of formula (II): (BH 4 ) (1+y) -L y -N x (II),
wherein: L represents an alkali metal selected from the group consisting of lithium, sodium and potassium, N represents a molecule of an ether, x is equal to or greater than 0, and y is an integer equal to or greater than 0.

8. A catalytic composition according to claim 1 , wherein the rare earth metal is a lanthanide, the atomic number of which varies from 57 to 71.

9. A catalytic composition according to claim 1 , wherein the rare earth metal is neodymium Nd.

10. A catalytic composition according to claim 1 , wherein the bridge P corresponds to the formula ZR 1 R 2 , Z representing a silicon or carbon atom and R 1 and R 2 , which are identical or different, each representing an alkyl group comprising from 1 to 20 carbon atoms.

11. A catalytic composition according to claim 10 , wherein Z is Si.

12. A catalytic composition according to claim 1 , wherein the metallocene is the (dimethylsilyl)bisfluorenylneodymium borohydride of formula (III): [Me 2 Si(Flu) 2 Nd(μ-BH 4 ) 2 Li(THF)] (III) Flu representing the C 13 H 18 group.

13. A catalytic composition according to claim 1 , wherein the conjugated diene is a 1,3-diene.

14. A catalytic composition according to claim 13 , wherein the conjugated diene is 1,3-butadiene or isoprene.

15. A catalytic composition according to claim 1 , wherein the molar ratio of the preformation monomer to the metal of the metallocene has a value ranging from 5 to 1000.

16. A catalytic composition according to claim 1 , wherein the molar ratio of cocatalyst to the metal of the metallocene has a value ranging from 0.5 to 20.

17. A catalytic composition according to claim 1 , which catalytic composition comprises a hydrocarbon solvent.

18. A catalytic composition according to claim 17 , wherein the hydrocarbon solvent is aromatic or aliphatic.

19. A catalytic composition according to claim 17 , wherein the molar concentration of metal of the metallocene in the catalytic solution has a value ranging from 0.0001 to 0.05 mol/l.

20. A catalytic composition according to claim 1 , wherein the metallocene is of formula (Ia).

21. A process for the preparation of a catalytic composition defined in claim 1 , which comprises the following stages:
a) reacting, in a hydrocarbon solvent, the cocatalyst and the metallocene, and
b) reacting the preformation monomer with the reaction product from stage a).

22. A process according to claim 21 , wherein stage a) takes place at a temperature ranging from 20° C. to 80° C. and stage b) is carried out at a temperature ranging from 40° C. to 120° C.

23. A process for the preparation of a polymer which comprises the polymerization of a monomer M in the presence of a catalytic composition defined in claim 1 , in which the monomer M is selected from the group of the monomers consisting of conjugated dienes, ethylene, α-olefins and their mixtures.

24. A process according to claim 23 , wherein the monomer M is at least one of a 1,3-diene and isoprene.

25. A process according to claim 23 , wherein the monomer M is 1,3-butadiene or a mixture of 1,3-butadiene and ethylene.

26. A process according to claim 23 , wherein the polymer is an elastomer.

Assignees

• Michelin & Cie

Inventors

• Lafaquiere Vincent
• Thuilliez Julien

Classifications

• C07F5/00 Primary

  Compounds containing elements of Groups 3 or 13 of the Periodic Table · CPC title

• C08F236/06

  Butadiene · CPC title

• C07F17/00

  Metallocenes · CPC title

• C08F2420/01

  Cp or analog bridged to a non-Cp X neutral donor · CPC title

• C08F236/08

  Isoprene · CPC title