IP Library Granted Patent US 8,680,274
Granted Patent B2
US 8,680,274 · App. 12/812,423 · Granted Mar 25, 2014

Bent allenes, and their metal complexes

Inventors: Guy Bertrand (Riverside, CA); Vincent Lavallo (Riverside, CA); Adam C. Dyker (Riverside, CA)
Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 8,680,274
App. No.
12/812,423
Granted
Mar 25, 2014
Kind
B2
Abstract

Stable, bent allenes, organometallic complexes of bent allenes are provided along with methods of conducting chemical processes such as olefin metathesis, comprising contacting an olefin substrate with an organometallic complex as described herein, under suitable conditions.

Claims (27)

1. An organometallic complex comprising a metal atom selected from groups 1-16 of the periodic table and a C—C—C bent allene two- to four-electron-donating ligand having the formula:

wherein each of R a , R b , R c and R d are independently selected from the group consisting of hydrogen, C 1-10 alkyl, C 3-10 cycloalkyl, C 2-10 alkenyl, C 3-10 cycloalkenyl, C 2-10 alkynyl, C 2-10 alkoxycarbonyl, C 1-10 alkylsulfonyl, C 1-10 alkylsulfinyl, aryl-C 1-4 alkyl and heteroaryl-C 1-4 alkyl; and each R e is a substituent independently selected from the group consisting of halogen, cyano, nitro, C 1-4 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 alkoxy, C 2-6 alkenyloxy, C 2-6 alkynyloxy, C 2-6 alkoxycarbonyl, C 1-6 alkylthio, C 1-6 alkylsulfonyl, C 1-6 alkylsulfinyl, primary amino, carboxyl, C 1-6 alkylamino, C 1-6 dialkylamino, amido, hydroxy and thiol groups.

2. An organometallic complex comprising a metal atom selected from groups 1-16 of the periodic table and a C—C—C bent allene two- to four-electron-donating ligand having the formula:

wherein the subscripts n are each independently an integer of from 0 to 4; and

each R e is a substituent independently selected from the group consisting of halogen, cyano, nitro, C 1-4 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 alkoxy, C 2-6 alkenyloxy, C 2-6 alkynyloxy, C 2-6 alkoxycarbonyl, C 1-6 alkylthio, C 1-6 alkylsulfonyl, C 1-6 alkylsulfinyl, primary amino, carboxyl, C 1-6 alkylamino, C 1-6 dialkylamino, amido, hydroxy and thiol groups.

3. A reaction mixture comprising an organometallic complex of claim 1 , a solvent and an olefin substrate, wherein said olefin substrate is selected to participate in an olefin metathesis reaction.

4. A reaction mixture of claim 3 , wherein said olefin substrate is selected as a substrate for ring closing metathesis.

5. A reaction mixture of claim 3 , wherein said olefin substrate is selected as a substrate for ring opening polymerization metathesis.

6. A reaction mixture of claim 3 , wherein said olefin substrate is selected as a substrate for cross metathesis.

7. A reaction mixture of claim 3 , wherein said olefin substrate is selected as a substrate for acyclic diene polymerization metathesis.

8. A method for conducting olefin metathesis, comprising contacting an olefin substrate with an organometallic complex of claim 1 , under metathesis conditions.

9. A method of claim 8 , wherein said olefin substrate is selected as a substrate for ring closing metathesis.

10. A method of claim 8 , wherein said olefin substrate is selected as a substrate for ring opening polymerization metathesis.

11. A method of claim 8 , wherein said olefin substrate is selected as a substrate for cross metathesis.

12. A method of claim 8 , wherein said olefin substrate is selected as a substrate for acyclic diene polymerization metathesis.

13. A reaction mixture comprising an organometallic complex of claim 2 , a solvent and an olefin substrate, wherein said olefin substrate is selected to participate in an olefin metathesis reaction.

14. A reaction mixture of claim 13 , wherein said olefin substrate is selected as a substrate for ring closing metathesis.

15. A reaction mixture of claim 13 , wherein said olefin substrate is selected as a substrate for ring opening polymerization metathesis.

16. A reaction mixture of claim 13 , wherein said olefin substrate is selected as a substrate for cross metathesis.

17. A reaction mixture of claim 13 , wherein said olefin substrate is selected as a substrate for acyclic diene polymerization metathesis.

18. A method for conducting olefin metathesis, comprising contacting an olefin substrate with an organometallic complex of claim 2 , under metathesis conditions.

19. A method of claim 18 , wherein said olefin substrate is selected as a substrate for ring closing metathesis.

20. A method of claim 18 , wherein said olefin substrate is selected as a substrate for ring opening polymerization metathesis.

21. A method of claim 18 , wherein said olefin substrate is selected as a substrate for cross metathesis.

22. A method of claim 18 , wherein said olefin substrate is selected as a substrate for acyclic diene polymerization metathesis.

23. An organometallic complex of claim 1 , wherein said metal atom is selected from the group consisting of silver, gold, molybdenum, platinum, palladium, iron, nickel, iridium, ruthenium and rhodium.

24. An organometallic complex of claim 2 , wherein said metal atom is selected from the group consisting of silver, gold, molybdenum, platinum, palladium, iron, nickel, iridium, ruthenium and rhodium.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 16, 2011
From: UNIVERSITY OF CALIFORNIA
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 026754/0212 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 10, 2010
From: BERTRAND, GUY; LAVALLO, VINCENT; DYKER, ADAM C.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 025117/0379 →
Continuity (2)
Provisional Application 61020309 · Jan 10, 2008
Related Publication 20110021775A1 · Jan 27, 2011