US4180525A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Trans-halo(acyl)bis(triethylphosphine) nickel(II) complexes
Assignee: Phillips Petroleum Co
•
Filing: 1978-08-03
•
Granted: 1979-12-25
•
Expires: 1998-08-03
Abstract
Abstract A process for oligomerizing monoolefins using a catalyst system comprising at least one organoaluminum halide and at least one trans-halo(acyl)bis(triethylphosphine nickel(II) complex.
Inventors
- 👤 Darryl R. Fahey
- 👤 John E. Mahan
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-02 06:02
CPC Classifications
C; C07; C07F; C07F9/00; C07F9/02; C07C; C07C2/00; C07C2/02; C07C2/04; C07C2/06; C07C2/08; C07C2/26; C07C2/36; C07C5/00; C07C5/02; C07C5/03; C07C9/00; C07C9/14; C07C2531/00; C07C2531/16; C07C2531/22
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
175 words
A process for oligomerizing monoolefins comprising contacting under suitable reaction conditions at least one said monoolefin with a catalyzing amount of a catalyst system comprising (1) at least one organoaluminum halide compound having the formula R" n ALX 3-n' wherein each R" is a hydrocarbyl radical having from 1 to 20 carbon atoms; each X is a halogen; and n is 1, 1.5, or 2; and (2) at least one acyl nickel complex having the formula ##STR5## wherein X is a halogen; PEt 3 is triethylphosphine; and R is selected from the group consisting of alkyl hydrocarbon radicals containing 6 to 12 carbon atoms; substituted aryl radicals containing 6 to 12 carbon atoms and having as the only non-hydrocarbon substituents 1 or 2 halogens selected from fluorine, chlorine, and bromine bonded to the aromatic portion of the aryl radical; and substituted aralkyl radicals containing 7 to 12 carbon atoms and having as the only nonhydrocarbon substituents one or more halogens selected from fluorine, chlorine and bromine bonded to the aromatic portion of the aralkyl radical.
Claim 2
Dependent Claim
175 words
A process for oligomerizing monoolefins comprising contacting under suitable reaction conditions at least one said monoolefin with a catalyzing amount of a catalyst system comprising (1) at least one organoaluminum halide compound having the formula R" n ALX 3-n' wherein each R" is a hydrocarbyl radical having from 1 to 20 carbon atoms; each X is a halogen; and n is 1, 1.5, or 2; and (2) at least one acyl nickel complex having the formula ##STR5## wherein X is a halogen; PEt 3 is triethylphosphine; and R is selected from the group consisting of alkyl hydrocarbon radicals containing 6 to 12 carbon atoms; substituted aryl radicals containing 6 to 12 carbon atoms and having as the only non-hydrocarbon substituents 1 or 2 halogens selected from fluorine, chlorine, and bromine bonded to the aromatic portion of the aryl radical; and substituted aralkyl radicals containing 7 to 12 carbon atoms and having as the only nonhydrocarbon substituents one or more halogens selected from fluorine, chlorine and bromine bonded to the aromatic portion of the aralkyl radical.
Claim 3
Dependent Claim
51 words
A process according to claim 1 wherein the mole ratio of said organoaluminum halide compound to said acyl nickel complex is in the range of about 0.5:1 to about 20:1 and the mole ratio of said nickel complex to said monoolefin is in the range of about 0.00001:1 to about 0.1:1.
Claim 4
Dependent Claim
31 words
A process according to claim 2 wherein said at least one monoolefin is selected from monoolefins having 2 to 12 carbon atoms and no branching on a doubly bonded carbon atom.
Claim 5
Dependent Claim
36 words
A process according to claim 3 wherein said contacting is carried out in the temperature range of about -80° to about 200° C. and in the pressure range of about 0 psig to about 2000 psig.
Claim 6
Dependent Claim
11 words
A process according to claim 4 wherein said monoolefin is propylene.
Claim 7
Dependent Claim
21 words
A process according to claim 5 wherein said acyl nickel complex is trans-chloro(4-chlorobenzoyl)bis(triethylphosphine)nickel(II) and said organoaluminum halide compound is methylaluminum sesquichloride.
Claim 8
Dependent Claim
37 words
A process according to claim 4 wherein said at least one nickel complex is selected from the group consisting of trans-chloro(1-adamantanecarbonyl)bis(triethylphosphine)nickel(II), trans-chloro(pivaloyl)bis(triethylphosphine)nickel(II), trans-chloro(4-chlorobenzoyl)bis(triethylphosphine) nickel(II), trans-chloro(3-chlorobenzoyl)bis(triethylphosphine)nickel(II), trans-chloro(benzoyl)bis(triethylphosphine)nickel(II), trans-chloro(3,3-dimethylbutanoyl)bis(triethylphosphine)nickel(II), trans-chloro(2-chlorobenzoyl)bis (triethylphosphine)nickel(II), trans-chloro(acetyl)bis(triethylphosphine) nickel(II), trans-bromo(benzoyl)bis(triethylphosphine)nickel(II), trans-fluoro (benzoyl)bis(triethylphosphine)nickel(II), and trans-chloro(1-naphthoyl)bis (triethylphosphine)nickel(II).
Claim 9
Dependent Claim
44 words
A process according to claim 7 wherein said at least one organoaluminum halide compound is selected from the group consisting of methylaluminum dichloride, dimethylaluminum chloride, diethylaluminum bromide, ethylaluminum dibromide, vinylaluminum diiodide, dibutylaluminum chloride, phenylaluminum dibromide, dibenzylaluminum chloride, 4-tolyaluminum dichloride, dodecylaluminum dibromide, and methylaluminum sesquichloride.
Claim 10
Dependent Claim
11 words
A process according to claim 8 wherein said monoolefin is propylene.
Claim 11
Dependent Claim
18 words
A process according to claim 9 wherein said at least one organoaluminum halide compound is methyl aluminum sesquichloride.
References Cited (Backward Citations)
US3636128A
Cited
US4000211A
Cited
US3689588A
Cited
US3907923A
Cited
US3800000A
Cited
US3808246A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1982-12-24 | 1983-06-25 | 1983-12-25 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1986-12-24 | 1987-06-25 | 1987-12-25 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1990-12-24 | 1991-06-25 | 1991-12-25 | $7700.00 | Window Closed / Lapsed |