Olefin conversion

Claim 2

A disproportionation process which comprises contacting a suitable olefinic reactant with a catalyst comprising a dicarbonyl(cyclopentadienyl)nitrosyl complex of molybdenum or tungsten and an alkylaluminum halide.

Claim 3

The process of claim 1, wherein said olefinic reactants contain from about 2 to 40 carbon atoms and one or more non-conjugated carbon-carbon double bonds per molecule and are either (1) an acyclic olefin of the formula: R.sub.1 CH═CHR.sub.2 wherein R 1 and R 2 are independently selected from the group consisting of hydrogen, alkyl radicals, alkaryl radicals and alkenyl radicals where each of said radicals contains 1 to 18 carbon atoms, or (2) a monocyclic olefin represented by the formula: ##STR2## wherein R 3 is an alkylene or alkenylene radical containing 3 to about 16 carbon atoms per radical.

Claim 4

The process of claim 2 wherein said olefinic reactants are selected from propane, 1-butene, 1-pentene, 2-pentene, 1-hexene, 2-hexene, 1-octene, 2-octene, 4-methyl-1-heptene, 2-nonene, 1-decene, 2-decene, 1-dodecene, 6-dodecene, 1-tetracene, 1-eicosene, 1,4-hexadiene, 4-phenyl-1-butene, 4-phenyl-1-octene, cyclopentene, cyclooctene, cyclononene, cyclotetradecene, 1,5-cyclododecadiene and 1,6-cyclodecadiene.

Claim 5

The process of claim 1 wherein said catalyst is a dicarbonyl(cyclopentadiene)nitrosyl complex of molybdenum or tungsten having the formula: LM(CO).sub.2 NO wherein L is (R) n C 5 H 5-n ; n is 0-5; R is a monovalent alkyl radical having from 1 to 4 carbon atoms and M is molybdenum or tungsten.

Claim 6

The process of claim 4 wherein said dicarbonyl(cyclopentadiene)nitrosyl catalyst is selected from the group consisting of (C 5 H 5 )Mo(CO) 2 NO; (C 5 H 5 )W(CO) 2 NO; (CH 3 C 5 H 4 )Mo(CO) 2 NO; (CH 3 C 5 H 4 )W(CO) 2 NO; [(CH 3 ) 5 C 5 ]Mo(CO) 2 NO; and [(CH 3 ) 5 C 5 ]W(CO) 2 NO.

Claim 7

The process of claim 1 wherein said alkylaluminum halide is an alkylaluminum halide of the formula: RAlX.sub.2 or R.sub.3 Al.sub.2 X.sub.3 wherein R is a monovalent linear alkyl radical having up to at least 4 carbon atoms and X is chlorine, bromine or iodine.

Claim 8

The process of claim 6 wherein said alkylaluminum halide is selected from ethylaluminum dichloride or ethylaluminum sesquichloride.

Claim 9

The process of claim 1 wherein said disproportionation is carried out in the temperature range of about 0° C. to about 140° C. and under pressure in the range of about 5 psig to about 5000 psig.

Claim 10

The process of claim 1 wherein the molar ratio of olefinic reactant to catalyst is in the range of about 1:1 to about 1000:1.

Claim 11

The process of claim 1 wherein the molar ratio of olefinic reactant to alkylaluminum halide is from about 1:1 to 1000:1.

Claim 12

The process of claim 1 wherein said reaction is carried out in the presence of a diluent.

Claim 13

The process of claim 11 wherein said diluent is selected from saturated hydrocarbons, aromatic hydrocarbons and halogenated hydrocarbons.

Claim 14

The process of claim 12 wherein said diluent is chlorobenzene.

Claim 15

The process of claim 11 wherein the volume ratio of diluent to olefinic reactant is from about 1000:1 to about 1:1000.

Claim 16

The process of claim 1 wherein 2-octene is reacted to produce 2-butene and 6-dodecene.

Claim 17

The process of claim 1 wherein 1-hexene is reacted to produce ethylene and 5-decene.