Catalytic composition comprising nickel, a phosphine-type ligand and a Lewis base, and use thereof in an olefin oligomerisation method

Patent metadata

Field	Value
Publication number	US-10646860-B2
Application number	US-201616062725-A
Country	US
Kind code	B2
Filing date	Dec 13, 2016
Priority date	Dec 18, 2015
Publication date	May 12, 2020
Grant date	May 12, 2020

Abstract

The invention concerns a catalytic composition comprising: at least one nickel precursor with an oxidation number of (+II), at least one phosphine ligand with formula PR1R2R3 in which the groups R1, R2 and R3, which may be identical or different and which may or may not be bonded together, and at least one Lewis base, said composition having a molar ratio of the phosphine ligand to the nickel precursor of less than or equal to 5 and a molar ratio of the Lewis base and phosphine ligand together to the nickel precursor of greater than or equal to 5.

First claim

The invention claimed is:

1. A catalytic composition comprising:
a at least one nickel compound with an oxidation number of (+II),
b at least one phosphine ligand with formula PR 1 R 2 R 3 , in which the groups R 1 , R 2 and R 3 , which may be identical or different, and which may or may not be bonded together, are selected from:
aromatic groups which may or may not be substituted and which may or may not contain heteroelements,
and/or from hydrocarbyl groups, which may or may not be cyclic, which may or may not be substituted and which may or may not contain heteroelements,

c an activating agent selected from the group formed by chlorine- and bromine-containing compounds of hydrocarbyl aluminum, used alone or as a mixture, and
d at least one Lewis base,
wherein said composition having a molar ratio of the phosphine ligand to the nickel compound of less than or equal to 5, a molar ratio of the Lewis base and phosphine ligand together to the nickel compound comprised of between 5 to 30, and a molar ratio of the activating agent to the nickel compound of greater than or equal to 6.

2. The composition as claimed in claim 1 , in which the molar ratio of the phosphine ligand to the nickel compound is in the range 2 and 5.

3. The composition as claimed in claim 1 , in which the nickel compound is selected from nickel(II) chloride; nickel(II) (dimethoxyethane) chloride; nickel(II) bromide; nickel(II) (dimethoxyethane) bromide; nickel(II) fluoride; nickel(II) iodide; nickel(II) sulphate; nickel(II) carbonate; nickel(II) dimethylglyoxime; nickel(II) hydroxide; nickel(II) hydroxyacetate; nickel(II) oxalate; nickel(II) carboxylates selected from the group formed by nickel(II) 2-ethylhexanoate; nickel(II) acetate; nickel(II) trifluoroacetate; nickel(II) triflate; nickel(II) acetylacetonate; nickel(II) hexafluoroacetylacetonate; nickel(II) phenates; allylnickel(II) chloride; allylnickel(II) bromide; the dimer of methallylnickel(II) chloride; allylnickel(II) hexafluorophosphate; methallylnickel(II) hexafluorophosphate; biscyclopentadienyl nickel(II); bisallyl nickel(II) and bismethallyl nickel(II); in their hydrated form or otherwise; used alone or as a mixture.

4. The composition as claimed in claim 1 , in which the nickel compound is selected from nickel(II) sulphate; nickel(II) carbonate; nickel(II) dimethylglyoxime; nickel(II) hydroxide; nickel(II) hydroxyacetate; nickel(II) oxalate; nickel(II) carboxylates selected from the group formed by nickel(II) 2-ethylhexanoate; nickel(II) acetate; nickel(II) trifluoroacetate; nickel(II) triflate; nickel(II) acetylacetonate; nickel(II) hexafluoroacetylacetonate; nickel(II) phenates; allylnickel(II) hexafluorophosphate; methallylnickel(II) hexafluorophosphate; nickel(II); bisallyl nickel(II) and bismethallyl nickel(II); in their hydrated form or otherwise, used alone or as a mixture.

5. The composition as claimed in claim 1 , in which the groups IV, R 2 and R 3 of said phosphine ligand are identical.

6. The composition as claimed in claim 1 , in which the aromatic groups R 1 , R 2 and R 3 of the phosphine ligand PR 1 R 2 R 3 are selected from the group formed by the following groups: phenyl, o-tolyl, m-tolyl, p-tolyl, mesityl, 3,5-dimethylphenyl, 4-n-butylphenyl, 4-methoxyphenyl, 2-methoxyphenyl, 3-methoxyphenyl, 4-methoxyphenyl, 2-isopropoxyphenyl, 4-methoxy-3,5-dimethylphenyl, 3,5-di-tert-butyl-4-methoxyphenyl, 4-chlorophenyl, 3,5-di(trifluoromethyl)phenyl, benzyl, naphthyl, bisnaphthyl, pyridyl, bisphenyl, furanyl and thiophenyl.

7. The composition as claimed in claim 1 , in which the hydrocarbyl groups R 1 , R 2 and R 3 of the phosphine ligand PR 1 R 2 R 3 contain 1 to 20 carbon atoms.

8. The composition as claimed in claim 7 , in which the hydrocarbyl groups IV, R 2 and R 3 of the phosphine ligand PR 1 R 2 R 3 are selected from the group formed by the following groups: methyl, ethyl, propyl, isopropyl, n-butyl, tert-butyl, cyclopentyl, cyclohexyl, benzyl, adamantyl.

9. The composition as claimed in claim 1 , in which the Lewis base is selected from diethylether, methyl tert-butylether, tetrahydrofuran, 1,4-dioxane, isoxazole, pyridine, pyrazine and pyrimidine.

10. The composition as claimed in claim 1 , in which the said activating agent is selected from the group formed by methylaluminium dichloride (MeAlCl 2 ), ethylaluminium dichloride (EtAlCl 2 ), ethylaluminium sesquichloride (Et 3 Al 2 Cl 3 ), diethylaluminium chloride (Et 2 AlCl), diisobutylaluminium chloride (iBu 2 AlCl) and isobutylaluminium dichloride (iBuAlCl 2 ), used alone or as a mixture.

11. The composition as claimed in claim 1 , in which the molar ratio of the activating agent to the phosphine ligand is greater than or equal to 1.

12. A process for the oligomerization of a feed of olefins, comprising contacting said feed of olefins with the catalytic composition of claim 1 to form a product.

13. The process as claimed in claim 12 , in which the feed comprises olefins containing in the range 2 to 10 carbon atoms.

14. The process as claimed in claim 12 , carried out in a closed system, in a semi-open system, continuously or batchwise.

15. The process as claimed in claim 12 , in which said process is a process for the dimerization of ethylene.

16. The process of claim 12 further comprising:
adding said product to a fuel for automobiles.

Assignees

• Ifp Energies Now

Inventors

• Breuil Pierre-Alain
• Chaumet-Martin Olivia

Classifications

• C07C2531/14

  of aluminium or boron · CPC title

• B01J2531/847

  Nickel · CPC title

• C07C2/36

  as phosphines, arsines, stilbines or bismuthines · CPC title

• C10G2400/20

  C2-C4 olefins · CPC title

• C07C6/02

  Metathesis reactions at an unsaturated carbon-to-carbon bond · CPC title