Dinitrosyldihalo complexes of molybdenum or tungsten

Claim 2

A process for the preparation of dinitrosyldihalo complexes of a metal selected from molybdenum and tungsten which comprises contacting (I) at least one oxytetrahalide of molybdenum or tungsten, (II) at least one alkali metal nitrite, (III) a reducing agent selected from elemental iron, borohydrides of sodium, potassium, rubidium, and cesium, and mixtures, (IV) at least one ligand-forming compound, and (V) at least one aprotic diluent, employing effective ratios of each material, and employing effective conditions of temperature, pressure, and time.

Claim 3

The process according to claim 1 wherein said (I) oxytetrahalide of molybdenum or tungsten can be represented by MOX 4 wherein M is molybdenum or tungsten, and each X is a halogen and is individually selected from fluorine, chlorine, bromine, and iodine.

Claim 4

The process according to claim 2 wherein said (I) molybdenum or tungsten oxytetrahalide is molybdenum oxytetrafluoride, molybdenum oxytetrachloride, molybdenum oxytetrabromide, molybdenum oxytetraiodide, molybdenum oxydichloridedibromide, tungsten oxytetrafluoride, tungsten oxytetrachloride, tungsten oxytetrabromide, tungsten oxytetraiodide, tungsten oxybromidetriiodide, or mixture.

Claim 5

The process according to claim 1 wherein said (II) alkali metal nitrite is the nitrite of lithium, sodium, potassium, rubidium, or cesium, or mixtures thereof.

Claim 6

The process according to claim 1 wherein said (III) reducing agent is said elemental iron and is a finely divided elemental iron.

Claim 7

The process according to claim 1 wherein said (III) reducing agent is a said borohydride.

Claim 8

The process according to claim 1 wherein said (IV) ligand-forming component is (A) at least one monodentate ligand-forming compound selected from the group consisting of tertiary aryl and alkaryl phosphines, arsines, and stibines, and heterocyclic nitrogen-containing compounds of the pyridine-, quinoline-, and isoquinoline-type; (B) at least one bidentate ligand-forming compound of the 2,2'-bipyridyl type; or (C) mixture.

Claim 9

The process according to claim 7 wherein said (IV) ligand-forming compound is (A) a said monodentate ligand-forming compound which is heterocyclic nitrogen compound which is a pyridine-type compound, quinoline-type compound, or isoquinoline-type compound.

Claim 10

The process according to claim 8 wherein said (IV) monodentate ligand-forming compound is a heterocyclic nitrogen-containing compound wherein said pyridine-type compound, quinoline-type compound, and isoquinoline-type compound can each be represented by the formulae, respectively: ##STR3## wherein each R is individually selected from hydrogen and alkyl radicals such as the total number of carbon atoms in each such compound is from 5 to 15.

Claim 11

The process according to claim 9 wherein said (IV) monodentate ligand-forming compound is a pyridine-type compound selected from the group consisting of pyridine, 2-methylpyridine, 4-ethylpyridine, 2-methyl-5-ethylpyridine, 4-isopropylpyridine, 3-hexylpyridine, 4-decylpyridine, pentamethylpyridine, and mixtures.

Claim 12

The process according to claim 9 wherein said (IV) monodentate ligand-forming compound is a quinoline-type compound selected from the group consisting of quinoline, 2-methylquinoline, 4-ethyl-6-isopropylquinoline, 8-hexylquinoline, 2,3,4,5,6,7-hexamethyl-quinoline, and mixtures.

Claim 13

The process according to claim 9 wherein said (IV) monodentate ligand-forming compound is a said isoquinoline-type compound selected from the group consisting of isoquinoline, 3-methylisoquinoline, 1-ethyl-4-isobutylisoquinoline, 5-hexylisoquinoline, 1,4,5,6,7,8-hexamethylisoquinoline, and mixtures.

Claim 14

The process according to claim 7 wherein said (IV) ligand-forming compound is (A) a monodentate ligand-forming compound and is a compound of phosphorus, arsenic, or antimony represented by R' 3 Q wherein said Q is phosphorus, arsenic, or antimony, and each R' is individually selected from aryl and alkaryl radicals containing 6 to 12 carbon atoms per R' group.

Claim 15

The process according to claim 13 wherein said (IV) R' 3 Q is selected from the group consisting of triphenylphosphine, triphenylarsine, triphenylstibine, tri-2-naphthylphosphine, tri-3-biphenylylarsine, diphenyl-o-tolylstibine, tri-p-tolylphosphine, tris(3-ethylphenyl)arsine, tris(4-isopropylphenyl)stibine, tris(3-hexylphenyl)phosphine, tris(4-methyl-1-naphthyl)arsine, tris(2-methyl-5-isopropylphenyl)stibine, tris(pentamethylphenyl)phosphine, and mixtures.

Claim 16

The process according to claim 7 wherein said (IV) ligand-forming compound is a (B) bidentate ligand-forming compound and is a bipyridyl-type compound represented by the formula: ##STR4## wherein each R and each R" is hydrogen or alkyl, with the proviso that the two R" groups together can represent a --CR═CR-- group, and such that the total number of carbon atoms per bipyridyl-type compound is 10 to 15.

Claim 17

The process according to claim 15 wherein said (IV) compound bi-pyridyl is selected from the group consisting of 2,2'-bipyridyl, 3-methyl-2,2'-bipyridyl, 4,4'-dimethyl-2,2'-bipyridyl, 5-ethyl-6'-isopropyl-2,2'-bipyridyl, 5-pentyl-2,2'-bipyridyl, 3,3',4,4',5-pentamethyl-2,2'-bipyridyl, 4-isopropyl-1,10-phenanthroline, 1,10-phenanthroline, 3-methyl-1,10-phenanthroline, or mixtures.

Claim 18

The process according to claim 17 wherein said (IV) ligand-forming compound is triphenylphosphine, triphenylarsine, triphenylstibine, tri-2-naphthylphosphine, tri-3-biphenylylarsine, diphenyl-o-tolylstibine, tri-p-tolylphosphine, tris(3-ethylphenyl)arsine, tris(4-isopropylphenyl)stibine, tris(3-hexylphenyl)phosphine, tris(4-methyl-1-naphthyl)arsine, tris(2-methyl-5-isopropylphenyl)stibine, tris(pentamethylphenyl)-phosphine, pyridine, 2-methylpyridine, 4-ethylpyridine, 2-methyl-5-ethylpyridine, 4-isopropylpyridine, 3-hexylpyridine, 4-decylpyridine, pentamethylpyridine, quinoline, 2-methylquinoline, 4-ethyl-6-isopropylquinoline, 8-hexylquinoline, 2,3,4,5,6,7-hexamethylquinoline, isoquinoline, 3-methylisoquinoline, 1-ethyl-4-isobutylisoquinoline, 5-hexylisoquinoline, 1,4,5,6,7,8-hexamethylisoquinoline, 2,2'-bipyridyl, 3-methyl-2,2'-bipyridyl, 4,4'-dimethyl-2,2'-bipyridyl, 5-ethyl-6'-isopropyl-2,2'-bipyridyl, 5-pentyl-2,2'-bipyridyl, 3,3',4,4',5-pentamethyl-2,2'-bipyridyl, 1,10-phenanthroline, 3-methyl-1,10-phenanthroline, or mixtures.

Claim 19

The process according to claim 1 wherein said (V) aprotic diluent is an ether, chlorinated saturated aliphatic hydrocarbon, or halogenated aromatic hydrocarbon.

Claim 20

The process according to claim 18 wherein said (IV) aprotic solvent is diethyl ether, dibutyl ether, dihexyl ether, dicyclohexyl ether, diphenyl ether, dimethyl ether of ethylene glycol, tetrahydrofuran, p-dioxane, methylene chloride, chloroform, carbon tetrachloride, ethylene dichloride, butyl chloride, hexyl chloride, or chlorobenzene, bromobenzene, chlorotoluene, bromotoluene, o-dichlorobenzene, or mixture.

Claim 21

The process according to claim 7 employing a mole ratio of (II) alkali metal nitrite:(I) oxytetrahalide in the mole ratio range of about 1:1 to 4:1; a mole ratio of (III) reducing agent:(I) oxytetrahalide in the mole ratio range of about 1:1 to 5:1; wherein when said (IV) ligand-forming component is a said (A) monodentate ligand-forming compound, employing a mole ratio of (A) monodentate ligand-forming compound:(I) oxytetrahalide in the mole ratio range of about 1:1 to 4:1, and wherein when said (IV) ligand-forming component is a said (B) bidentate ligand-forming compound, employing a ratio of (B) bidentate ligand-forming compound:(I) oxytetrahalide in the mole ratio range of about 0.5:1 to 2:1; and employing about 5 to 200 milliliters of said (V) aprotic diluent per gram of (I) oxytetrahalide employed.

Claim 22

The process according to claim 20 employing a mole ratio of (II) alkali metal nitrite:(I) oxytetrahalide of about 1.8:1 to 2.2:1; a mole ratio of (III) reducing agent:(I) oxytetrahalide of about 2:1 to 3:1; wherein when said (IV) ligand-forming component is a said (A) monodentate ligand-forming compound, employing a ratio of (A) monodentate ligand-forming compound:(I) oxytetrahalide in the mole ratio range of about 1.8:1 to 2.2:1, and wherein when said (IV) ligand-forming component is a said (B) bidentate ligand-forming compound, employing a mole ratio of said (B) bidentate-forming compound:(I) oxytetrahalide of about 0.9:1 to 1.1:1; and employing about 10 to 60 milliliters of said (V) aprotic diluent per gram of (I) oxytetrahalide employed.

Claim 23

The process according to claim 21 employing a contacting temperature in the range of about 0° to 200° C.

Claim 24

The process according to claim 1 wherein said dinitrosyldihalo complex produced is bis(triphenylphosphine)dinitrosyldichloromolybdenum, bis(triphenylstibine)dinitrosyldibromomolybdenum, bis(tri-3-biphenylylarsine)dinitrosyldifluoromolybdenum, bis(tri-p-tolylphosphine)dinitrosyldibromomolybdenum, bis[tris(3-hexylphenyl)phosphine]dinitrosyldiiodomolybdenum, bis[tris(2-methyl-5-isopropylphenyl)stibine]dinitrosyldichloromolybdenum, di(pyridine)dinotrosyldichloromolybdenum, bis(2-methyl-5-ethylpyridine)dinitrosyldiiodomolybdenum, bis(3-hexylpyridine)dinitrosyldichloromolybdenum, bis(pentamethylpyridine)dinitrosyldiiodomolybdenum, bis(2-methylquinoline)dinitrosyldichloromolybdenum, bis(8-hexylquinoline)dinitrosyldiiodomolybdenum, di(isoquinoline)dinitrosyldichloromolybdenum, bis(1-ethyl-4-isobutylisoquinoline)dinitrosyldiiodomolybdenum, bis(1,4,5,6,7,8-hexamethylisoquinoline)dinitrosyldichloromolybdenum, (3-methyl-2,2'-bipyridyl)dinitrosyldiiodomolybdenum, (5-ethyl-6'-isopropyl-2,2'-bipyridyl)dinitrosyldichloromolybdenum, (3,3',4,4',5-pentamethyl-2,2'-bipyridyl)dinitrosyldiiodomolybdenum, (1,10-phenanthroline)dinitrosyldichloromolybdenum, (4-isopropyl-1,10-phenanthroline)dinitrosyldifluoromolybdenum, or mixture.

Claim 25

The process according to claim 1 wherein said dinitrosyldihalo complex produced is bis(triphenylarsine)dinitrosyldifluorotungsten, bis(tri-2-naphthylphosphine)dinitrosyldiiodotungsten, bis(diphenyl-o-tolylstibine)dinitrosyldichlorotungsten, [tris(3-ethylphenyl)arsine][tris(4-isopropylphenyl)stibine]dinitrosylchlorobromotungsten, bis[tris(4-methyl-1-naphthyl)arsine]dinitrosyldifluorotungsten, bis[tris(pentamethylphenyl)phosphine]dinitrosyldibromotungsten, bis(2-methylpyridine)dinitrosyldibromotungsten, bis(4-isopropylpyridine)dinitrosyldifluorotungsten, bis(4-decylpyridine)dinitrosyldibromotungsten, di(quinoline)dinitrosyldifluorotungsten, bis(4-ethyl-6-isopropylquinoline)dinitrosyldibromotungsten, bis(2,3,4,5,6,7-hexamethylquinoline)dinitrosyldifluorotungsten, bis(3-methylisoquinoline)dinitrosyldibromotungsten, bis(5-hexylisoquinoline)dinitrosyldifluorotungsten, (2,2'-bipyridyl)dinitrosyldibromotungsten, (4,4'-dimethyl-2,2'-bipyridyl)dinitrosyldifluorotungsten, (5-pentyl-2,2'-bipyridyl)dinitrosyldibromotungsten, (3-methyl-1,10-phenanthroline)dinitrosyldibromotungsten, or mixture.

Claim 26

The process according to claim 1 wherein said dinitrosyldihalo complex produced is bis(triphenylphosphine)dinitrosyldichloromolybdenum, bis(tri-2-naphthylphosphine)dinitrosyldiiodotungsten, bis(tri-p-tolylphosphine)dinitrosyldibromomolybdenum, bis[tris(3-hexylphenyl)phosphine]dinitrosyldiiodomolybdenum, bis[tris(pentamethylphenyl)phosphine]dinitrosyldibromotungsten, or mixture.

Claim 27

The process according to claim 1 wherein said dinitrosyldihalo complex produced is bis(triphenylarsine)dinitrosyldifluorotungsten, bis(tri-3-biphenylylarsine)dinitrosyldifluoromolybdenum, [tris(3-ethylphenyl)arsine][tris(4-isopropylphenyl)stibine]dinitrosylchlorobromotungsten, bis[tris(4-methyl-1-naphthyl)arsine]dinitrosyldifluorotungsten, or mixture.

Claim 28

The process according to claim 1 wherein said dinitrosyldihalo complex produced is bis(triphenylstibine)dinitrosyldibromomolybdenum, bis(diphenyl-o-tolylstibine)dinitrosyldichlorotungsten, bis[tris(2-methyl-5-isopropylphenyl)stibine]dinitrosyldichloromolybdenum, [tris(3-ethylphenyl)arsine][tris(4-isopropylphenyl)stibine]dinitrosylchlorobromotungsten, or mixture.

Claim 29

The process according to claim 1 wherein said dinitrosyldihalo complex produced is bis(2-methylpyridine)dinitrosyldibromotungsten, bis(2-methyl-5-ethylpyridine)dinitrosyldiiodomolybdenum, bis(4-isopropylpyridine)dinitrosyldifluorotungsten, bis(3-hexylpyridine)dinitrosyldichloromolybdenum, bis(4-decylpyridine)dinitrosyldibromotungsten, bis(pentamethylpyridine)dinitrosyldiiodomolybdenum, or mixture.

Claim 30

The process according to claim 1 wherein said dinitrosyldihalo complex produced is di(quinoline)dinitrosyldifluorotungsten, bis(2-methylquinoline)dinitrosyldichloromolybdenum, bis(4-ethyl-6-isopropylquinoline)dinitrosyldibromotungsten, bis(8-hexylquinoline)dinitrosyldiiodomolybdenum, bis(2,3,4,5,6,7-hexamethylquinoline)dinitrosyldifluorotungsten, or mixture.

Claim 31

The process according to claim 1 wherein said dinitrosyldihalo complex produced is di(isoquinoline)dinitrosyldichloromolybdenum, bis(3-methylisoquinoline)dinitrosyldibromotungsten, bis(1-ethyl-4-isobutylisoquinoline)dinitrosyldiiodomolybdenum, bis(5-hexylisoquinoline)dinitrosyldifluorotungsten, bis(1,4,5,6,7,8-hexamethylisoquinoline)dinitrosyldichloromolybdenum, or mixture.

Claim 32

The process according to claim 1 wherein said dinitrosyldihalo complex produced is (2,2'-bipyridyl)dinitrosyldibromotungsten, (3-methyl-2,2'-bipyridyl)dinitrosyldiiodomolybdenum, (4,4'-dimethyl-2,2'-bipyridyl)dinitrosyldifluorotungsten, (5-ethyl-6'-isopropyl-2,2'-bipyridyl)dinitrosyldichooromolybdenum, (5-pentyl-2,2'-bipyridyl)dinitrosyldibromotungsten, (3,3',4,4'5-pentamethyl-2,2'-bipyridyl)dinitrosyldiiodomolybdenum, (1,10-phenanthroline)dinitrosyldichloromolybdenum, (3-methyl-1,10-phenanthroline)ditrosyldibromotungsten, (4-isopropyl-1,10-phenanthroline)dinitrosyldifluoromolybdenum, or mixture.

Claim 33

The process according to claim 22 wherein said (I) oxytetrahalide is molybdenum oxytetrachloride, said (II) alkali metal nitrite is sodium nitrite, said (III) reducing agent is iron powder, said (IV) ligand-forming material is triphenylphosphine, and said (V) aprotic diluent is tetrahydrofuran, and wherein the dinitrosyldihalo complex of molybdenum or tungsten so produced is bis(triphenylphosphine)dinitrosyldichloromolybdenum.

Claim 34

The process according to claim 22 wherein said (I) oxytetrahalide is molybdenum oxytetrachloride, said (II) alkali metal nitrite is potassium nitrite, said (III) reducing agent is sodium borohydride, said (IV) ligand-forming material is triphenylphosphine, and said (V) aprotic diluent is tetrahydrofuran, and wherein the dinitrosyldihalo complex of molybdenum or tungsten so produced is bis(triphenylphosphine)dinitrosyldichloromolybdenum.