IP Library Granted Patent US 7,030,051
Granted Patent B2
US 7,030,051 · App. 10/229,378 · Granted Apr 18, 2006

Dirhodium catalyst compositions and methods for using same

Assignee: The Research Foundation of State University of New York
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Quick Facts
Patent No.
US 7,030,051
App. No.
10/229,378
Granted
Apr 18, 2006
Kind
B2
Abstract

Disclosed is method for increasing the efficiency of a dirhodium catalyst. The method includes providing a dirhodium catalyst, providing an organic ester, and contacting the dirhodium catalyst and the organic ester under conditions effective to increase the efficiency of the dirhodium catalyst. The organic ester is selected such that it is not a substrate for catalysis by the dirhodium catalyst. Dirhodium catalyst compositions which include a dirhodium catalyst and an organic ester are also disclosed. In these compositions, the organic ester is not a substrate for catalysis by the dirhodium catalyst. The method and compositions can be used in a number of reactions, including insertion reactions (e.g., C—H insertions, Si—H insertions, O—H insertions, and N—H insertions) cyclopropanation reactions, annulations (e.g., [3+2] annulations and [3+4] annulations), and ω,ω-diarylalkanoate syntheses.

Claims (34)

1. A dirhodium catalyst composition comprising:

a dirhodium catalyst; and

an organic ester, wherein said organic ester is not a substrate for catalysis by said dirhodium catalyst and wherein said organic ester is an ester of an aryl acid.

2. A composition according to claim 1 , wherein said organic ester is an ester of a benzoic acid or an ester of a naphthoic acid.

3. A composition according to claim 1 , wherein said organic ester is an ester of a benzoic acid.

4. A composition according to claim 1 , wherein said organic ester is a C1–C12 alkyl ester of a benzoic acid.

5. A composition according to claim 1 , wherein said organic ester has the formula C 6 H 5 COOW and wherein W is a C1–C12 alkyl group.

6. A composition according to claim 1 , wherein said organic ester has the formula C 6 H 5 COOW and wherein W is a C1–C4 alkyl group.

7. A composition according to claim 1 , wherein said organic ester has the formula C 6 H 5 COOW and wherein W is a methyl group.

8. A composition according to claim 1 , wherein said dirhodium catalyst is a dirhodium tetracarboxylate catalyst.

9. A composition according to claim 8 , wherein the dirhodium tetracarboxylate catalyst is selected from the group consisting of dirhodium acetate dimer, dirhodium propionate dimer, dirhodium butyrate dimer, dirhodium pentanoate dimer, dirhodium hexanoate dimer, dirhodium heptanoate dimer, dirhodium octanoate dimer, fluorinated analogs thereof, and combinations thereof.

10. A composition according to claim 8 , wherein the dirhodium tetracarboxylate catalyst has the formula:

wherein each of M 1 and M 2 is Rh; Z 4 represents the atoms necessary to complete a 3–12 membered heterocyclic ring; and Q 3 is an electron withdrawing group.

11. A composition according to claim 10 , wherein Z 4 has the formula —CH 2 CH 2 CH 2 —.

12. A composition according to claim 11 , wherein the dirhodium tetracarboxylate catalyst has one of the following formulae:

13. A composition according to claim 12 , wherein the dirhodium catalyst has D 2 symmetry.

14. A composition according to claim 8 , wherein the dirhodium tetracarboxylate catalyst has the formula:

wherein each of M 1 and M 2 is Rh; Z 2 and Z 3 , independently, are the atoms necessary to complete a 3–12 membered heterocyclic ring; Z 1 is an alkylene or arylene group; Q 1 and Q 2 are the same or different and are electron withdrawing groups; L 1 and L 3 , taken together, represent —O—CR 13 —O—; L 2 and L 4 , taken together, represent —O—CR 14 —O—; and R 13 and R 14 are the same or different and are selected from the group consisting of alkyl groups and aryl groups or R 13 and R 14 represent alkylene or arylene groups that are directly or indirectly bonded to one another.

15. A composition according to claim 14 , wherein the dirhodium tetracarboxylate catalyst has the formula:

16. A composition according to claim 14 , wherein Z 2 and Z 3 each have the formula —CH 2 CH 2 —.

17. A composition according to claim 14 , wherein Z 1 is 1,3-phenylene.

18. A composition according to claim 14 , wherein the dirhodium tetracarboxylate catalyst has one of the following formulae:

19. A composition according to claim 14 , wherein the dirhodium tetracarboxylate catalyst has one of the following formulae:

wherein R 1 and R 2 are the same or different and are alkyl or aryl groups.

20. A dirhodium catalyst composition a comprising:

a dirhodium catalyst; and

an organic ester, wherein said organic ester is not a substrate for catalysis by said dirhodium catalyst and wherein said organic ester and said dirhodium catalyst are present in a mole ratio of from 0.01:1 to 10 8 :1.

21. A composition according to claim 20 , wherein said organic ester and said dirhodium catalyst are present in a mole ratio of from 0.1:1 to 10 7 :1.

22. A composition according to claim 20 , wherein said organic ester and said dirhodium catalyst are present in a mole ratio of from 1000:1 to 10 6 :1.

23. A composition according to claim 20 , wherein said organic ester and said dirhodium catalyst are present in a mole ratio of from 0.01:1 to 10 8 :1 and wherein said organic ester is an ester of a benzoic acid or an ester of a naphthoic acid.

24. A composition according to claim 1 , wherein said organic ester and said dirhodium catalyst are present in a mole ratio of from 0.01:1 to 10 8 :1.

25. A composition according to claim 1 , wherein said organic ester and said dirhodium catalyst are present in a mole ratio of from 0.1:1 to 10 7 :1.

26. A composition according to claim 1 , wherein said organic ester and said dirhodium catalyst are present in a mole ratio of from 1000:1 to 10 6 :1.

27. A composition according to claim 1 , wherein said organic ester and said dirhodium catalyst are present in a mole ratio of from 0.01:1 to 10 8 :1 and wherein said organic ester is an ester of a benzoic acid or an ester of a naphthoic acid.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 9, 2015
From: STATE UNIVERSITY OF NEW YORK AT BUFFALO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036575/0668 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2002
From: DAVIES, HUW M.L.
To: RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK, THE
Reel/Frame 013554/0067 →
Continuity (2)
Provisional Application 6031515000 · Aug 27, 2001
Related Publication 20030130536A1 · Jul 10, 2003