Metal-ligand catalyst formation

Patent metadata

Field	Value
Publication number	US-9981257-B2
Application number	US-201213490207-A
Country	US
Kind code	B2
Filing date	Jun 6, 2012
Priority date	Jun 10, 2011
Publication date	May 29, 2018
Grant date	May 29, 2018

Abstract

As described herein, nickel treated with sulfur provides a surprisingly effective source of nickel atoms for generating nickel-phosphorus-containing ligand complexes useful as hydrocyanation catalysts.

First claim

What is claimed:

1. A method of generating a complex between nickel atoms and one or more phosphorus-containing ligands comprising:
a) contacting at least one of:
i) a nickel starting material having a sulfur concentration less than 0.4 wt % relative to the weight of the nickel starting material with a sulfur source, and reducing the nickel starting material to nickel metal from a mixture of the nickel starting material and the sulfur source to form a particulate sulfur-containing nickel metal; and
ii) a nickel metal having a sulfur concentration less than 0.4 wt % relative to the weight of the nickel metal with a sulfur source to form a particulate sulfur-containing nickel metal;
the contacting comprising adding the sulfur source to the nickel starting material or nickel metal;
wherein the nickel starting material is basic nickel carbonate, nickel carbonate, nickel bicarbonate, nickel oxalate, nickel formate, nickel squarate, nickel hydroxide, nickel oxide, or a combination thereof, and the sulfur in the sulfur source contacted with the nickel starting material or with the nickel metal is 0.1 wt % to 50 wt % relative to the total weight of nickel in the nickel starting material or in the nickel metal;
wherein the sulfur source is elemental sulfur, a disulphide, thioacetic acid, a thioacetate salt, a polysulfide, a bis-alkylamino disulphide, a sulfenic sulfonic thioanhydride, a thiosulfonate salt, an aminothiosulfonate, an acylmethylmercapto azole, an acylmethylmercapto-azolium salt, a thiazepine, a thiepin, a 1,4-dithiin, a 1,2-thiazine, a 1,3-thiazine, a 1,4-thiazine, a 1,4,2-dithiazine, a 1,3,4-thiadiazine, a 1,2,6-thiadiazine, a 1,3,5-thiadiazine, a dihydro-dithiazine, a dihydrothiadiazine, a 1,2,3,4-thiatriazole, sulfur trioxide, sulfur dioxide, sulfur monoxide, disulfur dichloride, sulfur dichloride, sulfur tetrachloride, sulfur chloride pentafluoride, disulfur decafluoride, sulfur hexafluoride, sulfur tetrafluoride, sulfur trifluoride, or a combination thereof; and

b) contacting the particulate sulfur-containing nickel metal with one or more phosphorus-containing ligand(s) to thereby form a complex between nickel atoms from the nickel metal and one or more phosphorus-containing ligands.

2. The method of claim 1 , further comprising determining a sulfur content of the nickel starting material or the nickel metal before contacting the nickel metal or the nickel starting material with the sulfur source.

3. The method of claim 1 , wherein the nickel metal in step (ii) is simultaneously contacted with the sulfur source and one or more phosphorus-containing ligand(s).

4. The method of claim 1 , wherein the sulfur source is 95% to 99.9% free of silicon, sodium, potassium, calcium, magnesium, phosphorus, aluminium, copper, tungsten, mercury, iron, and combinations thereof.

5. The method of claim 1 , wherein the nickel starting material or nickel metal is 95% to 99.9% free of silicon, sodium, potassium, calcium, magnesium, phosphorus, aluminium, copper, tungsten, mercury, iron and combinations thereof.

6. The method of claim 1 , wherein the nickel metal or the nickel starting material is contacted with the sulfur source before reduction of the nickel starting material or the nickel metal to zero valent nickel.

7. The method of claim 1 , wherein the nickel starting material is reduced in hydrogen at 200° C. to 400° C. for 3 to 5 hours.

8. The method of claim 1 , wherein a complex forms between nickel atoms from the particulate sulfur-containing nickel metal and one or more phosphorus-containing ligands in the presence of a Lewis acid.

9. The method of claim 1 , wherein equilibrium of complex formation between nickel atoms from the particulate sulfur-containing nickel metal and one or more phosphorus-containing ligands is reached by 2 hours when 4% nickel is mixed at 60° C. to 80° C. in an organonitrile solvent with 0.5 to 2.5 moles Lewis acid per mole phosphorus-containing ligand.

10. The method of claim 1 , wherein the complex at least partially dissolved in an organonitrile solvent.

11. The method of claim 10 , wherein the organonitrile solvent is a pentenenitrile.

12. The method of claim 1 , wherein one or more of the phosphorus ligands is a ligand of Formula (III):

wherein:
X 11 , X 12 , X 13 , X 21 , X 22 and X 23 independently represent oxygen or a single direct bond;
R 11 and R 12 independently represent identical or different, single or bridged organic radicals;
R 21 and R 22 independently represent identical or different, single or bridged organic radicals; and
Y represents a bridging group.

13. The method of claim 1 , wherein one or more of the phosphorus ligands is Ligand (V):

14. The method of claim 1 , wherein contacting generates a sulfur to nickel atomic ratio of 0.003 to 1.8.

15. The method of claim 1 , wherein the complex formed between nickel atoms from the particulate sulfur-containing nickel metal and one or more phosphorus-containing ligands catalyses hydrocyanation of an olefin.

16. The method of claim 15 , wherein the olefin is pentenenitrile.

17. The method of claim 1 , wherein the particulate sulfur-containing nickel metal comprises nickel crystallites with a BET Specific Surface Area of at least 1 m 2 /gm, and/or wherein on average there are at least 10 15 surface crystallites present per gram nickel, as calculated for substantially cuboidal crystallites.

18. The method of claim 1 , wherein the particulate sulfur-containing nickel metal comprises 0.001 wt % to 15 wt % sulfur, wherein the sulfur weight percentage is relative to the total weight of nickel in the particulate sulfur-containing nickel metal.

19. The method of claim 1 , wherein the particulate sulfur-containing nickel metal is contacted with the one or more phosphorus-containing ligands in the presence of an organonitrile solvent.

20. The method of claim 1 , wherein the particulate sulfur-containing nickel metal is contacted with the one or more phosphorus-containing ligands in the presence of a Lewis acid.

21. The method of claim 20 , wherein the Lewis acid is selected from the group consisting of zinc chloride, ferrous chloride, and a combination thereof.

22. The method of claim 21 , wherein the zinc to phosphorus-containing ligand molar ratio is 0.5 to 2.5.

23. The method of claim 1 , wherein the particulate sulfur-containing nickel metal is contacted with and the one or more phosphorus-containing ligands at 2 wt % to 8 wt %.

24. The method of claim 1 , wherein the particulate sulfur-containing nickel metal at 1 wt % to 7 wt % is contacted with the one or more phosphorus-containing ligands.

25. The method of claim 1 , wherein the complex comprises 0.00001 wt % to 15 wt % sulfur in the complex wherein the sulfur weight percentage is relative to the total weight of nickel in the complex.

26. The method of claim 25 , wherein the complex comprises 0.0001 wt % to 1 wt % sulfur in the complex.

27. The method of claim 1 , wherein the particulate sulfur-containing nickel metal comprises a nickel particulate form comprising nickel crystallites and 0.2 wt % to 12 wt % sulfur, wherein the nickel particulate form has a BET Specific Surface Area of at least 1 m 2 /gm; at least 10%

Assignees

• Fraga Dubreuil Joan
• Medhekar Vinay
• Micka Thomas A
• Whiston Keith
• Ostermaier John J
• Slaten Colin S
• Invista North America Sarl

Inventors

• Fraga-Dubreuil Joan
• Medhekar Vinay
• Micka Thomas A
• Whiston Keith
• Ostermaier John J
• Slaten Colin S

Classifications

• B01J31/1845 Primary

  the ligands containing phosphorus (phosphines B01J31/24) · CPC title

• B01J31/2409

  with more than one complexing phosphine-P atom · CPC title

• B01J2231/322

  Hydrocyanation · CPC title

• C07C253/10

  to compounds containing carbon-to-carbon double bonds · CPC title

• B01J23/755

  Nickel · CPC title