IP Library Granted Patent US 8,623,928
Granted Patent B2
US 8,623,928 · App. 13/509,630 · Granted Jan 7, 2014

Polymers of intrinsic microporosity containing tetrazole groups

Inventors: Naiying Du (Ottawa, CA); Michael D. Guiver (Ottawa, CA)
Assignee: National Research Council of Canada
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Quick Facts
Patent No.
US 8,623,928
App. No.
13/509,630
Granted
Jan 7, 2014
Kind
B2
Abstract

The invention provides a tetrazole-containing polymer of intrinsic microporosity comprising (10) or more subunits, wherein one or more of the subunits comprise one or more tetrazolyl moieties. In one embodiment, a polymer of intrinsic microporosity (PIM-1) was modified using a “click chemistry” [2+3] cycloaddition reaction with sodium azide and zinc chloride to yield new PIMs containing tetrazole units. Polymers of the present invention are useful as high-performance materials for membrane-based gas separation, materials for ion exchange resins, materials for chelating resins, materials for superabsorbents, materials for ion conductive matrixes, materials for catalyst supports or materials for nanoparticle stabilizers.

Claims (21)

1. A tetrazole-containing polymer of intrinsic microporosity comprising 10 or more subunits, wherein one or more of the subunits comprise one or more tetrazolyl moieties.

2. The polymer according to claim 1 having a degree of tetrazole substitution in a range of from 0.01 to 1.

3. The polymer according to claim 1 having a degree of tetrazole substitution in a range of from 0.1 to 1.

4. The polymer according to claim 1 having a general structure encompassed by Formula I:

where x is an integer of 10 or greater and A represents a subunit in the polymer, wherein one or more of the subunits comprises one or more tetrazolyl moieties, and wherein A for each subunit is independently

5. The polymer according to claim 4 , wherein A is independently

provided that one or more of the subunits comprises one or more tetrazolyl moieties.

6. The polymer according to claim 4 , wherein tetrazolyl is a moiety having a structure encompassed by general Formula (II) or a tautomer thereof:

where R1 is H, alkyl, aralkyl, arylsulfonyl, alkylsulfonyl or an ionic liquid group.

7. The polymer according to claim 6 , wherein R1 is H, C 1 -C 6 -alkyl, C 7 -C 13 -aralkyl, C 7 -C 13 -arylsulfonyl, C 1 -C 6 -alkylsulfonyl or C 1 -C 20 -organic amine.

8. The polymer according to claim 6 , wherein R1 is H, benzyl, 4-acetamidobenezenesulfonyl, methylamine, diisopropylamine or N,N-diisopropylethylamine.

9. The polymer according to claim 4 , wherein x is an integer in a range from 10 to 10,000.

10. The polymer according to claim 4 ,wherein x is an integer in a range from 40 to 1500.

11. The polymer according to claim 4 , wherein x is an integer in a range from 40 to 1000.

12. The polymer according to claim 1 comprising 10 to 10,000 subunits.

13. The polymer according to claim 1 comprising 40 to 1000 subunits.

14. A film comprising a polymer according to claim 1 .

15. The film according to claim 14 for use in gas separation, vapor separation, adsorbents or catalysis.

16. The film according to claim 14 for use in oxygen enrichment, natural gas treatment or carbon dioxide capture from emissions.

17. The film according to claim 14 for use in carbon dioxide capture from emissions.

18. Use of the polymer as defined in claim 1 as a material for membrane-based gas separation, a material for ion exchange resins, a material for chelating resins, a material for superabsorbents, a material for ion conductive matrixes, a material for catalyst supports or a material for nanoparticle stabilizers.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2012
From: DU, NAIYING; GUIVER, MICHAEL D.
To: NATIONAL RESEARCH COUNCIL OF CANADA
Reel/Frame 028200/0516 →
Continuity (2)
Provisional Application 61272861 · Nov 12, 2009
Related Publication 20120264589A1 · Oct 18, 2012