IP Library Granted Patent US 10,053,534
Granted Patent B2
US 10,053,534 · App. 15/398,545 · Granted Aug 21, 2018

Functionalization of Diels-Alder polyphenylene polymers

Inventor: Cy Fujimoto (Albuquerque, NM)
Assignee: National Technology & Engineering Solutions of Sandia, LLC
C08G61/10C08L65/00C08G2261/11C08G2261/146C08G2261/148C08G2261/312C08G2261/46C08G2261/516C08G2261/72C08G2261/722C08G2261/728
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Quick Facts
Patent No.
US 10,053,534
App. No.
15/398,545
Granted
Aug 21, 2018
Kind
B2
Abstract

The present invention relates to functionalized polymers including a poly(phenylene) structure. The structure can include any useful modifications, such as the inclusion of one or more reactive handles having an aryl group. Methods and uses of such structures and polymers are also described herein.

Claims (77)

1. A composition comprising a structure having the formula (II):

or a salt thereof, wherein:

each R H is, independently, H, optionally substituted C 1-12 alkyl, optionally substituted C 1-12 haloalkyl, optionally substituted C 1-12 perfluoroalkyl, optionally substituted C 1-12 heteroalkyl, halo, optionally substituted aryl, optionally substituted alkaryl, optionally substituted arylalkoxy, optionally substituted aryloxy, optionally substituted aryloxycarbonyl, optionally substituted aryloyl, optionally substituted arylcarbonylalkyl, optionally substituted arylsulfonyl, or optionally substituted arylsulfonylalkyl;

each R 1 and R 3 is, independently, H, halo, optionally substituted C 1-12 alkyl, optionally substituted C 1-12 haloalkyl, optionally substituted C 1-12 perfluoroalkyl, optionally substituted C 1-12 heteroalkyl, R S , R P , R C , or R F , wherein R S is an acidic moiety comprising a sulfonyl group, R P is an acidic moiety comprising a phosphoryl group, R C is an acidic moiety comprising a carbonyl group, and R F is an electron-withdrawing moiety;

each Ar L is, independently, a bivalent linker comprising optionally substituted arylene;

each Ar M is, independently, a bivalent linker comprising optionally substituted arylene;

each q is, independently, an integer of from 0 to 5;

each h is, independently, an integer of from 0 to 5, wherein at least one h is not 0;

m is an integer of from about 1 to 1000; and

wherein at least one R H on a pendent group of formula (II) comprises a substituted aryl group comprising halo or alkoxy or aryloxy.

2. The composition of claim 1 , wherein:

at least one R H is —L H —Ar H ;

L H is a covalent bond, carbonyl, oxy, thio, azo, phosphonoyl, phosphoryl, sulfonyl, sulfinyl, sulfonamide, imino, imine, phosphine, nitrilo, optionally substituted C 1-12 alkylene, optionally substituted C 1-12 alkyleneoxy, optionally substituted C 1-12 heteroalkylene, optionally substituted C 1-12 heteroalkyleneoxy, optionally substituted C 4-18 arylene, or optionally substituted C 4-18 aryleneoxy; and

Ar H is an optionally substituted aryl.

3. The composition of claim 2 , wherein L H is a covalent bond, carbonyl, sulfonyl, —NR L3 —, —(CR L1 R L2 ) La—, —C(O) NR L3 —, —NR L3 C(O)—, —SO 2 —NR L3 —, —NR L3 —SO 2 —, —(CR L1 R L2 ) La —C(O)—NR L3 —, —(CR L1 R L2 ) La —NR L3 —C(O)—, —(CR L1 R L2 ) La —SO 2 —NR L3 —, or —SO 2 —NR L3 —(CR L1 R L2 ) La —;

wherein each of R L1 , R L2 , and R L3 is, independently, H, optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted alkoxy, optionally substituted alkaryl, optionally substituted aryl, or halo; and

wherein Ar H is optionally substituted with one or more substituents selected from the group consisting of halo, cyano, optionally substituted haloalkyl, optionally substituted perfluoroalkyl, optionally substituted nitroalkyl, and optionally substituted alkyl.

4. The composition of claim 1 , wherein the composition comprises a structure having the formula (IIk):

or a salt thereof, wherein:

L H is a covalent bond, carbonyl, oxy, thio, azo, phosphonoyl, phosphoryl, sulfonyl, sulfinyl, sulfonamide, imino, imine, phosphine, nitrilo, optionally substituted C 1-12 alkylene, optionally substituted C 1-12 alkyleneoxy, optionally substituted C 1-12 heteroalkylene, optionally substituted C 1-12 heteroalkyleneoxy, optionally substituted C 4-18 arylene, or optionally substituted C 4-18 aryleneoxy; and

Ar H is an optionally substituted aryl.

5. The composition of claim 1 , wherein at least one R H is an optionally substituted C 4-18 aryl, optionally substituted C 1-6 alk-C 4-18 aryl, optionally substituted C 4-18 aryl-C 1-6 alkoxy, optionally substituted C 4-18 aryloxy, optionally substituted C 5-19 aryloxycarbonyl, optionally substituted C 5-19 aryloyl, optionally substituted C 4-18 arylcarbonyl-C 1-6 alkyl, optionally substituted C 4-18 arylsulfonyl, or optionally substituted C 4-18 arylsulfonyl-C 1-6 alkyl; and/or wherein at least one R H is optionally substituted C 4-18 aryloxy comprising one or more halo or haloalkyl.

6. The composition of claim 5 , wherein each and every R H comprises a substituted aryl group.

7. The composition of claim 1 , wherein:

R S is —SO 2 —R S1 or —SO 2 —NR N1 —R S2 or —SO 2 —NR N1 —SO 2 —R S3 , wherein each R S1 is, independently, H, optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted perfluoroalkyl, optionally substituted aryl, optionally substituted alkaryl, or hydroxyl; each R N1 is, independently, H or optionally substituted C 1-12 alkyl, optionally substituted aryl, or optionally substituted alkaryl; each R S2 is, independently, H, hydroxyl, optionally substituted alkyl, optionally substituted alkylsulfonyl, optionally substituted aryl, or optionally substituted alkaryl; and each R S3 is, independently, H, hydroxyl, optionally substituted alkyl, optionally substituted C 1-12 haloalkyl, optionally substituted perfluoroalkyl, optionally substituted aryl, or optionally substituted alkaryl;

R P is —P(O)(OH) 2 or —O—PO(OH) 2 or —P(O)<R P1 R P2 or —P(O)<R Ar R P2 or —P(O)<R Ar R Ar , and wherein each of R P1 and R P2 is, independently, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted aryl, optionally substituted alkaryl, optionally substituted aryloxy, hydroxyl, or H; and each of R Ar is, independently, optionally substituted aryl, optionally substituted alkaryl, or optionally substituted aryloxy;

R C is —CO 2 H, —C(O)—R C1 , or —R CA —C(O)—R C1 , and wherein each R C1 is, independently, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted aryl, optionally substituted alkaryl, optionally substituted aryloxy, hydroxyl, or H; and each R CA is, independently, oxy, optionally substituted alkylene, or optionally substituted heteroalkylene; and

R F is optionally substituted aryloyl, carboxyaldehyde, optionally substituted alkanoyl, or optionally substituted alkyl.

8. The composition of claim 1 , wherein Ar L and/or Ar M is optionally substituted phenylene, optionally substituted naphthylene, or optionally substituted phenanthrylene.

9. The composition of claim 8 , wherein the optional substitution for Ar L is R H , R S , R P , R C , or R F ; and wherein the optional substitution for Ar M is R H , R S , R P , R C , R F , or a label.

10. The composition of claim 1 , wherein the composition comprises a structure having formula (IIj):

or a salt thereof, wherein:

each of Ar L and Ar M is, independently, an optionally substituted phenylene.

11. The composition of claim 1 , wherein the composition comprises a structure having any one of formulas (II-1) to (II-10) and (II-13) to (II-18):

or a salt thereof; wherein:

each R H1 is, independently, H, halo, cyano, optionally substituted haloalkyl, optionally substituted perfluoroalkyl, optionally substituted nitroalkyl, or optionally substituted alkyl;

m is an integer of from about 1 to 500;

each Ak is, independently, an optionally substituted alkylene group; and

each h1 is, independently, an integer of from 1 to 12.

12. The composition of claim 1 , wherein:

at least one R H is —L H —Ar H ;

L H is a covalent bond, carbonyl, oxy, thio, azo, phosphonoyl, phosphoryl, sulfonyl, sulfinyl, sulfonamide, imino, imine, phosphine, nitrilo, optionally substituted C 1-12 alkylene, optionally substituted C 1-12 alkyleneoxy, optionally substituted C 1-12 heteroalkylene, optionally substituted C 1-12 heteroalkyleneoxy, optionally substituted C 4-18 arylene, or optionally substituted C 4-18 aryleneoxy; and

Ar H is a substituted aryl.

13. The composition of claim 12 , wherein the Ar H is a substituted phenyl.

14. The composition of claim 12 , wherein the Ar H is an R H1 -substituted phenyl group, and wherein R H1 is selected from the group consisting of an amino, amido, azido, nitro, nitroso, haloalkyl, and halo.

15. The composition of claim 12 , wherein L H is the covalent bond or carbonyl.

16. The composition of claim 1 , wherein the composition comprises a structure having formula (IIi):

or a salt thereof, wherein:

each of Ar L and Ar M is, independently, an optionally substituted phenylene and

each and every R H comprises a substituted aryl group.

17. The composition of claim 10 , wherein the composition comprises a structure having formula (IIj):

or a salt thereof, wherein:

each of Ar L and Ar M is, independently, an optionally substituted phenylene and

each and every R H comprises a substituted aryl group.

18. The composition of claim 4 , wherein each Ar H is substituted with one or more substituents selected from the group consisting of halo, cyano, optionally substituted haloalkyl, optionally substituted perfluoroalkyl, optionally substituted nitroalkyl, and optionally substituted alkyl.

19. The composition of claim 1 , wherein the composition comprises a structure having formula (IIq):

or a salt thereof, wherein:

L H is a covalent bond, carbonyl, oxy, thio, azo, phosphonoyl, phosphoryl, sulfonyl, sulfinyl, sulfonamide, imino, imine, phosphine, nitrilo, optionally substituted C 1-12 alkylene, optionally substituted C 1-12 alkyleneoxy, optionally substituted C 1-12 heteroalkylene, optionally substituted C 1-12 heteroalkyleneoxy, optionally substituted C 4-18 arylene, or optionally substituted C 4-18 aryleneoxy; and

each R H1 is, independently, selected from the group consisting of H, halo, cyano, amino, amido, azido, nitro, nitroso, optionally substituted haloalkyl, optionally substituted perfluoroalkyl, optionally substituted nitroalkyl, optionally substituted aminoalkyl, optionally substituted aryloxy, and optionally substituted alkyl.

20. The composition of claim 19 , wherein each R H1 is, independently, selected from the group consisting of H, halo, optionally substituted haloalkyl, optionally substituted aminoalkyl, and optionally substituted aryloxy.

21. A composition comprising a structure having the formula (III):

or a salt thereof, wherein:

L H is a covalent bond, carbonyl, oxy, thio, azo, phosphonoyl, phosphoryl, sulfonyl, sulfinyl, sulfonamide, imino, imine, phosphine, nitrilo, optionally substituted C 1-12 alkylene, optionally substituted C 1-12 alkyleneoxy, optionally substituted C 1-12 heteroalkylene, optionally substituted C 1-12 heteroalkyleneoxy, optionally substituted C 4-18 arylene, or optionally substituted C 4-18 aryleneoxy;

Ak H is a substituted alkyl or a substituted heteroalkyl, wherein each of the substituted alkyl or substituted heteroalkyl is substituted with one or more substituents selected from the group consisting of halo, cyano, amino, amido, azido, nitro, nitroso, optionally substituted haloalkyl, optionally substituted perfluoroalkyl, optionally substituted nitroalkyl, and optionally substituted alkyl;

each R 1 and R 3 is, independently, H, halo, optionally substituted C 1-12 alkyl, optionally substituted C 1-12 haloalkyl, optionally substituted C 1-12 perfluoroalkyl, optionally substituted C 1-12 heteroalkyl, R S , R P , R C , or R F , wherein R S is an acidic moiety comprising a sulfonyl group, R P is an acidic moiety comprising a phosphoryl group, R C is an acidic moiety comprising a carbonyl group, and R F is an electron-withdrawing moiety;

each Ar L is, independently, a bivalent linker comprising optionally substituted arylene;

each Ar M is, independently, a bivalent linker comprising optionally substituted arylene;

each q is, independently, an integer of from 0 to 5;

each h is, independently, an integer of from 0 to 5, wherein at least one h is not 0; and

m is an integer of from about 1 to 1000.

22. The composition of claim 21 , wherein the composition comprises a structure having formula (IIr):

or a salt thereof, wherein:

each R H1 is, independently, selected from the group consisting of halo, cyano, amino, amido, azido, nitro, nitroso, optionally substituted haloalkyl, optionally substituted perfluoroalkyl, optionally substituted nitroalkyl, and optionally substituted alkyl; and

each h1 is, independently, an integer of from 1 to 12.

23. The composition of claim 21 , wherein the composition comprises a structure having formulas (II-11) or (II-12):

or a salt thereof, wherein:

each h1 is, independently, an integer of from 1 to 12.

Assignments (6)
CORRECTIVE ASSIGNMENT TO CORRECT THE PROPERTY NUMBER PREVIOUSLY RECORDED AT REEL: 41356 FRAME: 224. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 6, 2020
From: FUJIMOTO, CY
To: NATIONAL TECHNOLOGY & ENGINEERING SOLUTIONS OF SANDIA, LLC
Reel/Frame 052116/0821 →
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NUMBER ON ATTACHMENT 15/398,547 AND FILING DATE SEPTEMBER 29,2016 PREVIOUSLY RECORDED ON REEL 041356 FRAME 0224. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Feb 20, 2020
From: FUJIMOTO, CY
To: NATIONAL TECHNOLOGY & ENGINEERING SOLUTIONS OF SANDIA, LLC
Reel/Frame 051977/0542 →
CHANGE OF NAME Recorded Apr 25, 2018
From: SANDIA CORPORATION
To: NATIONAL TECHNOLOGY & ENGINEERING SOLUTIONS OF SANDIA, LLC
Reel/Frame 046017/0963 →
CONFIRMATORY LICENSE Recorded Oct 31, 2017
From: SANDIA CORPORATION
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 044331/0613 →
CONFIRMATORY LICENSE Recorded Oct 2, 2017
From: SANDIA CORPORATION
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 044095/0034 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 23, 2017
From: FUJIMOTO, CY
To: SANDIA CORPORATION
Reel/Frame 041356/0224 →
Continuity (2)
Provisional Application 62274569 · Jan 4, 2016
Related Publication 20170190830A1 · Jul 6, 2017
Cited By (3)
US 12,258,440 US 12,318,770 US 12,448,508