IP Library Granted Patent US 8,633,123
Granted Patent B2
US 8,633,123 · App. 13/059,967 · Granted Jan 21, 2014

Catalysts and methods for polymer synthesis

Inventors: Scott D. Allen (Ithaca, NY); Anna E. Cherian (Ithaca, NY); Chris A. Simoneau (Ithaca, NY); Jay J. Farmer (Ithaca, NY); Geoffrey W. Coates (Ithaca, NY); Alexei Gridnev (Ithaca, NY); Robert E. LaPointe (Ithaca, NY)
Assignee: Novomer, Inc.
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Quick Facts
Patent No.
US 8,633,123
App. No.
13/059,967
Granted
Jan 21, 2014
Kind
B2
Abstract

The present invention provides unimolecular metal complexes having increased activity in the copolymerization of carbon dioxide and epoxides. Also provided are methods of using such metal complexes in the synthesis of polymers. According to one aspect, the present invention provides metal complexes comprising an activating species with co-catalytic activity tethered to a multidentate ligand that is coordinated to the active metal center of the complex.

Claims (55)

1. A metal complex of the formula:

wherein:

M is cobalt;

comprises a salen ligand; and

(Z) m represents one or more activating moieties tethered to the salen ligand, where represents a linker moiety; m represents the number of Z groups present on a linker moiety and is an integer between 1 and 4 inclusive; and each (Z) represents an activating moiety comprising a guanidine group.

2. The metal complex of claim 1 , where a guanidine group has a formula:

where each occurrence of R 1 , R 2 , R 2′ , and R 3 is independently hydrogen or an optionally substituted radical selected from the group consisting of C 1-20 aliphatic; C 1-20 heteroaliphatic; phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle, a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an 8- to 10-membered bicyclic heteroaryl ring having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; wherein any two or more R 1 , R 1′ , R 2 , R 2′ , and R 3 groups can be taken together with intervening atoms to form one or more optionally substituted rings optionally containing one or more additional heteroatoms.

3. The metal complex of claim 2 , wherein one or more of R 1 , R 2 , R 2′ , and R 3 , is H, or optionally substituted C 1-6 aliphatic.

4. The metal complex of claim 3 , wherein one or more of R 1 , R 2 , R 2′ , and R 3 , are methyl or ethyl.

5. The metal complex of claim 2 , wherein R 2 and R 2′ are taken together to form an optionally substituted ring.

6. The metal complex of claim 2 , wherein R 1 and R 3 are taken together to form optionally substituted rings.

7. The metal complex of claim 5 , wherein R 1 and R 3 are taken together to form an optionally substituted ring.

8. The metal complex of claim 7 , wherein the guanidine comprises:

9. The metal complex of claim 1 , wherein a guanidine is selected from the group consisting of:

10. The metal complex of claim 1 , wherein

comprises:

where

R 1a and R 1a′ are independently a (Z) m group, hydrogen, or an optionally substituted radical selected from the group consisting of: C 1-20 aliphatic; C 1-20 heteroaliphatic; phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle; a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen and sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 atoms independently selected from nitrogen, oxygen and sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms selected from nitrogen, oxygen and sulfur;

Rd at each occurrence is independently a (Z) m group, hydrogen, halogen, —OR, —NR 2 , —SR, —CN, —NO 2 , —SO 2 R, —SOR, —SO 2 NR 2 ; —CNO, —NRSO 2 R, —NCO, —N 3 , —SiR 3 ; or an optionally substituted radical selected from the group consisting of C 1-20 aliphatic; C 1-20 heteroaliphatic; phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle, a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an 8- to 10-membered bicyclic heteroaryl ring having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; where two or more Rd groups may be taken together with intervening atoms to form one or more optionally substituted rings optionally containing one or more heteroatoms,

R 4b is selected from the group consisting of:

where

R c at each occurrence is independently a (Z) m group, hydrogen, halogen, —OR, —NR 2 , —SR, —CN, —NO 2 , —SO 2 R, —SOR, —SO 2 NR 2 ; —CNO, —NRSO 2 R, —NCO, —N 3 , —SiR 3 ; or an optionally substituted radical selected from the group consisting of C 1-20 aliphatic; C 1-20 heteroaliphatic; phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle, a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an 8- to 10-membered bicyclic heteroaryl ring having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; where two or more R c groups may be taken together with the carbon atoms to which they are attached and any intervening atoms to form one or more optionally substituted rings; when two R c groups are attached to the same carbon atom, they may optionally be taken together along with the carbon atom to which they are attached to form an optionally substituted moiety selected from the group consisting of: a 3- to 8-membered spirocyclic ring, a carbonyl, an oxime, a hydrazone, and an imine;

Y is a divalent linker selected from the group consisting of: —NR—, —N(R)C(O)—, —C(O)NR—, —O—, —C(O)—, —OC(O)—, —C(O)O—, —S—, —SO—, —SO 2 —, —SiR 2 —, —C(═S)—, —C(═NR)—, or —N═N—; a polyether; a C 3 to C 8 substituted or unsubstituted carbocycle; and a C 1 to C 8 substituted or unsubstituted heterocycle;

R at each occurrence is independently hydrogen, an optionally substituted radical selected the group consisting of acyl; C 1-6 aliphatic; C 1-6 heteroaliphatic; carbamoyl; arylalkyl; phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle, a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an 8- to 10-membered bicyclic heteroaryl ring having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; an oxygen protecting group; and a nitrogen protecting group, where two R groups on the same nitrogen atom can optionally be taken together to form an optionally substituted 3- to 7-membered ring,

X is any anion;

m′ is 0 or an integer from 1 to 4, inclusive;

q is 0 or an integer from 1 to 4, inclusive; and

x is 0, 1, or 2.

11. The metal complex of claim 1 , wherein

is selected from the group consisting of:

where

represents an optionally substituted moiety linking the two nitrogen atoms, and is selected from the group consisting of: phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle, a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an 8- to 10-membered bicyclic heteroaryl ring having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an optionally substituted C 2-20 aliphatic group, wherein one or more methylene units are optionally and independently replaced by —NW—, —N(W)C(O)—, —C(O)N(W)—, —OC(O)N(R y )—, —N(R y )C(O)O—, —OC(O)O—, —O—, —C(O)—, —OC(O)—, —C(O)O—, —S—, —SO—, —SO 2 —, —C(═S)—, —C(═NR y )—, —C(═NOR y )— or —N═N where each occurrence of R y is independently selected from the group consisting of hydrogen an optionally substituted C 1-6 aliphatic group, and an optionally substituted aryl group;

R 4a , R 4a′ , R 5a , R 5a′ , R 6a′ , and R 6a′ are each independently a (Z) m group, hydrogen, halogen, —OR, —NR 2 , —SR, —CN, —NO 2 , —SO 2 R, —SOR, —SO 2 NR 2 ;

—CNO, —NRSO 2 R, —NCO, —N 3 , —SiR 3 ; or an optionally substituted radical selected from the group consisting of C 1-20 aliphatic; C 1-20 heteroaliphatic; phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle, a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an 8- to 10-membered bicyclic heteroaryl ring having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; wherein any two adjacent R 4a , R 4a′ , R 5a , R 5a′ , R 6a , and R 6a′ groups can be taken together with intervening atoms to form one or more optionally substituted rings,

R′ represents one or more substituents optionally present on the phenyl ring and each R′ is independently selected from the group consisting of: halogen, —NO 2 , —CN, —SR y , —S(O)R y , —S(O) 2 R y , —NR y C(O)R y , —OC(O)R y , —CO 2 R y , —NCO, —N 3 , —OR 7 , —OC(O)N(R y ) 2 , —N(R y ) 2 , —NR y C(O)R y , —NR y C(O)OR y ; or an optionally substituted radical selected from the group consisting of C 1-20 aliphatic; C 1-20 heteroaliphatic; phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle, a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an 8- to 10-membered bicyclic heteroaryl ring having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur, where two or more adjacent R′ groups can be taken together to form an optionally substituted saturated, partially unsaturated, or aromatic 5- to 12-membered ring containing 0 to 4 heteroatoms;

R at each occurrence is independently hydrogen, an optionally substituted radical selected the group consisting of acyl; C 1-6 aliphatic; C 1-6 heteroaliphatic; carbamoyl; arylalkyl; phenyl; a 3- to 8-membered saturated or partially unsaturated monocyclic carbocycle, a 7-14 carbon saturated, partially unsaturated or aromatic polycyclic carbocycle; a 5- to 6-membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturated heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; a 6- to 12-membered polycyclic saturated or partially unsaturated heterocycle having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; or an 8- to 10-membered bicyclic heteroaryl ring having 1-5 heteroatoms independently selected from nitrogen, oxygen, or sulfur; an oxygen protecting group; and a nitrogen protecting group, where two R groups on the same nitrogen atom can optionally be taken together to form an optionally substituted 3- to 7-membered ring,

R Y is —H, or an optionally substituted radical selected from the group consisting of C 1-6 aliphatic, 3- to 7-membered heterocyclic, phenyl, and 8- to 10-membered aryl;

X is any anion;

and

k is 1.

12. The metal complex of claim 11 , wherein the catalyst comprises a substructure of conforming to a formula selected from the group consisting of:

13. The metal complex of claim 12 , wherein comprises an optionally substituted C 2-30 aliphatic group wherein one or more methylene units are optionally and independently replaced by —NR y —, —N(R y )C(O)—, —C(O)N(R y )—, —O—, —C(O)—, —OC(O)—, —C(O)O—, —S—, —SO—, —SO 2 —, —C(═S)—, —C(═NR y )—, or —N═N—, where each occurrence of R y is independently —H, or an optionally substituted radical selected from the group consisting of C 1-6 aliphatic 3- to 7-membered heterocyclic, phenyl, and 8- to 10-membered aryl.

14. The metal complex of claim 12 , wherein comprises a C 3-30 aliphatic group.

15. The metal complex of claim 12 , wherein comprises a C 4-8 aliphatic group.

16. The metal complex of claim 12 , wherein comprises a C 3 aliphatic group.

17. The metal complex of claim 12 , wherein is selected from the group consisting of:

where * represents the site of attachment to the ligand, and each # represents a site of attachment the activating group.

18. The metal complex of claim 11 , wherein X is selected from the group consisting of: chlorine, bromine, an optionally substituted C 1-12 carboxylate, azide, an optionally substituted phenoxide, and sulfonate.

19. The metal complex of claim 17 , wherein X is selected from the group consisting of: chloride, acetate, trifluoroacetate, azide, pentafluorobenzoate, and a nitrophenolate.

20. A method for the synthesis of aliphatic polycarbonate polymers comprising the step of contacting one or more epoxides with carbon dioxide in the presence of a metal complex of claim 1 .

21. The method of claim 20 , wherein the epoxide is ethylene oxide, propylene oxide, or cyclohexene oxide.

22. The method of claim 21 , wherein the epoxide is ethylene oxide.

23. The method of claim 21 , wherein the epoxide is propylene oxide.

24. The method of claim 21 , wherein a pressure of carbon dioxide is between about 50 and 800 psi.

25. The method of claim 20 , wherein a molar ratio of catalyst to epoxide is between about 1:1000 and about 1:100,000.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2017
From: NOVOMER, INC.
To: SAUDI ARAMCO TECHNOLOGIES COMPANY
Reel/Frame 043194/0539 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 19, 2011
From: ALLEN, SCOTT D.; CHERIAN, ANNA E.; SIMONEAU, CHRIS A.; FARMER, JAY J.; COATES, GEOFFREY W.; GRIDNEV, ALEXEI; LAPOINTE, ROBERT E.
To: NOVOMER, INC.
Reel/Frame 026152/0061 →
Continuity (4)
Provisional Application 61091013 · Aug 22, 2008
Provisional Application 61096313 · Sep 11, 2008
Provisional Application 61098739 · Sep 19, 2008
Related Publication 20110152497A1 · Jun 23, 2011