Devices and methods for determination of species including chemical warfare agents
US-9267908-B2 · Feb 23, 2016 · US
US9770709B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9770709-B2 |
| Application number | US-201514670232-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 26, 2015 |
| Priority date | Nov 3, 2010 |
| Publication date | Sep 26, 2017 |
| Grant date | Sep 26, 2017 |
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The present invention generally relates to compositions comprising and methods for forming functionalized carbon-based nanostructures.
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What is claimed: 1. A catalyst composition for oxidation of carbon monoxide, comprising: a graphene or graphene oxide molecule comprising at least one functional group having the structure: wherein: R 1 , R 2 , and R 3 are the same or different and each is independently a substituent, optionally substituted, wherein at least one of R 1 , R 2 , and R 3 comprises a catalytic moiety capable of oxidizing carbon monoxide to carbon dioxide; and G is a carbon atom of the graphene or graphene oxide. 2. A catalyst composition as in claim 1 , wherein the catalytic moiety comprises a metal. 3. A catalyst composition as in claim 1 , wherein the catalytic moiety comprises Pd, Fe, Ce, Al, Cu, or Ti, or an oxide thereof. 4. A catalyst composition as in claim 1 , wherein the catalytic moiety comprises Pd nanoclusters, Fe 2 O 3 , FeOOH, or TiOOH. 5. A catalyst composition as in claim 2 , wherein at least one of R 1 , R 2 , and R 3 is capable of binding a metal. 6. A catalyst composition as in claim 5 , wherein at least one of R 1 , R 2 , and R 3 comprises nitrogen, sulfur, or phosphorus. 7. A catalyst composition as in claim 5 , wherein at least one of R 1 , R 2 , and R 3 comprises a positively or a negatively charged group. 8. A catalyst composition as in claim 1 , wherein the catalytic moiety is capable of reducing oxygen. 9. A catalyst composition as in claim 1 , wherein the catalytic moiety is capable of reducing nitric oxide. 10. A catalyst composition as in claim 1 , wherein: R 3 is hydrogen, alkyl, aryl, alkenyl, cycloalkyl, heteroalkyl, heteroaryl, N(R 4 ) 2 , SR 4 , Si(R 4 ) 2 , OR 4 , or OM, any of which is optionally substituted, M is a metal or cationic species; and each R 4 is independently a substituent, optionally substituted. 11. A catalyst composition as in claim 10 , wherein: R 3 is aryl, heteroalkyl, heteroaryl, N(R 4 ) 2 , SR 4 , Si(R 4 ) 2 , OR 4 , or OM, any of which is optionally substituted, M is a metal; and each R 4 is independently a substituent, optionally substituted. 12. A catalyst composition as in claim 11 , wherein each R 4 is independently hydrogen, an organic substituent, or a metal-containing substituent, optionally substituted. 13. A catalyst composition as in claim 10 , wherein R 3 is OR 4 or N(R 4 ) 2 . 14. A catalyst composition as in claim 10 , wherein each R 4 is the same or different and each is independently hydrogen, alkyl, cycloalkyl, haloalkyl, heteroalkyl, aryl, heteroaryl, or OH, any of which is optionally substituted. 15. A catalyst composition as in claim 10 , wherein R 3 is N(CH 3 ) 2 , NH-phenyl, NH-biphenyl, NHCH 2 (C≡CH), OH, OMe, OEt, OM, where M is a metal ion, OCH 2 (C≡CH), OCH 2 CH 2 (2-bromophenyl), OCH 2 (adamantyl), or OCH 2 C(4-chlorophenyl) 3 . 16. A catalyst composition as in claim 10 , wherein R 4 is alkyl substituted with an unsubstituted or substituted aryl or an unsubstituted or substituted cycloalkyl. 17. A catalyst composition as in claim 10 , wherein: R 1 and R 2 are the same or different and each is independently hydrogen, alkyl, heteroalkyl, cycloalkyl, alkenyl, or aryl, any of which is optionally substituted. 18. A catalyst composition as in claim 17 , wherein R 1 and R 2 are both hydrogen.
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