journal article·2015-12-22

Dual-Function Metal–Organic Framework as a Versatile Catalyst for Detoxifying Chemical Warfare Agent Simulants

Yangyang Liu, Su-Young Moon, Joseph T. Hupp, Omar K. Farha

ACS Nano· Volume 9· Issue 12
Publisher page

Abstract

The nanocrystals of a porphyrin-based zirconium(IV) metal-organic framework (MOF) are used as a dual-function catalyst for the simultaneous detoxification of two chemical warfare agent simulants at room temperature. Simulants of nerve agent (such as GD, VX) and mustard gas, dimethyl 4-nitrophenyl phosphate and 2-chloroethyl ethyl sulfide, have been hydrolyzed and oxidized, respectively, to nontoxic products via a pair of pathways catalyzed by the same MOF. Phosphotriesterase-like activity of the Zr6-containing node combined with photoactivity of the porphyrin linker gives rise to a versatile MOF catalyst. In addition, bringing the MOF crystals down to the nanoregime leads to acceleration of the catalysis.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Sulfur Compounds in Biology · Thermal and Kinetic Analysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States

Department of Chemistry, Faculty of Science, King Abdulaziz University, Jeddah 22254, Saudi Arabia

Funding

Defense Threat Reduction Agency

References (64)

Show source-provided references
1. Robinson J. P. · 1971
2. 10.1016/j.tox.2005.06.01110.1016/j.tox.2005.06.011 ↗
3. Karasik T. · 2002
4. 10.1021/cr00016a00310.1021/cr00016a003 ↗
5. Bajgar, J.; Fusek, J.; Kassa, J.; Kuca, K.; Jun, D.InHandbook of Toxicology of Chemical Warfare Agents;Gupta, R. C., Ed.Academic Press:San Diego, 2009; pp17–24.10.1016/B978-0-12-374484-5.00003-1 ↗
6. Johnson, N. H.; Larsen, J. C.; Meek, E.InHandbook of Toxicology of Chemical Warfare Agents;Gupta, R. C., Ed.Academic Press:San Diego, 2009; pp7–16.10.1016/B978-0-12-374484-5.00002-X ↗
7. Okumura, T.; Taki, K.; Suzuki, K.; Satoh, T.InHandbook of Toxicology of Chemical Warfare Agents;Gupta, R. C., Ed.Academic Press:San Diego, 2009; pp25–32.10.1016/B978-0-12-374484-5.00004-3 ↗
8. 10.1039/c3sc52259h10.1039/c3sc52259h ↗
9. Watson, A.; Opresko, D.; Young, R.; Hauschild, V.; King, J.; Bakshi, K.InHandbook of Toxicology of Chemical Warfare Agents;Gupta, R. C., Ed.Academic Press:San Diego, 2009; pp43–67.10.1016/B978-0-12-374484-5.00006-7 ↗
10. 10.1289/ehp.9910793310.1289/ehp.99107933 ↗
11. 10.1016/j.bbapap.2012.04.00410.1016/j.bbapap.2012.04.004 ↗
12. Pastel, R. H.; Ritchie, E. C.InPsychological Responses to the New Terrorism: A Nato-Russia Dialogue;IOS Press:Amsterdam, 2005; pp9–24.
13. 10.1016/j.tox.2005.06.01410.1016/j.tox.2005.06.014 ↗
14. 10.1067/mem.2001.11432210.1067/mem.2001.114322 ↗
15. 10.1016/0009-2797(94)90005-110.1016/0009-2797(94)90005-1 ↗
16. 10.1093/carcin/15.10.207510.1093/carcin/15.10.2075 ↗
17. 10.1016/j.bbapap.2012.04.00410.1016/j.bbapap.2012.04.004 ↗
18. 10.1021/bi700460c10.1021/bi700460c ↗
19. 10.1002/(SICI)1097-0290(19970420)54:2<105::AID-BIT2>3.0.CO;2-P10.1002/(SICI)1097-0290(19970420)54:2<105::AID-BIT2>3.0.CO;2-P ↗
20. 10.1021/cr100193y10.1021/cr100193y ↗
21. 10.1021/ic010702510.1021/ic0107025 ↗
22. 10.1021/ic061024v10.1021/ic061024v ↗
23. 10.1021/ja027728v10.1021/ja027728v ↗
24. 10.1039/c2cc17568a10.1039/c2cc17568a ↗
25. 10.1021/cs400173810.1021/cs4001738 ↗
26. 10.1021/jp302887910.1021/jp3028879 ↗
27. 10.1002/anie.20130752010.1002/anie.201307520 ↗
28. 10.1039/C4SC03613A10.1039/C4SC03613A ↗
29. 10.1038/nmat423810.1038/nmat4238 ↗
30. 10.1039/C5CC03398E10.1039/C5CC03398E ↗
31. 10.1002/anie.20150209410.1002/anie.201502094 ↗
32. 10.1016/j.micromeso.2015.01.01610.1016/j.micromeso.2015.01.016 ↗
33. Young, R. A.; Bast, C. B.InHandbook of Toxicology of Chemical Warfare Agents;Gupta, R. C., Ed.Academic Press:San Diego, 2009; p69.
34. 10.1021/ic00100a02810.1021/ic00100a028 ↗
35. 10.1021/ja992746710.1021/ja9927467 ↗
36. 10.1021/ja003313310.1021/ja0033133 ↗
37. 10.1021/ie010732f10.1021/ie010732f ↗
38. 10.1021/ja027475610.1021/ja0274756 ↗
39. 10.1021/cm051372f10.1021/cm051372f ↗
40. 10.1016/j.molcata.2005.10.00610.1016/j.molcata.2005.10.006 ↗
41. Hirade J. · J. Biochem. · 1950 · 37 · 1910.1093/oxfordjournals.jbchem.a126178 ↗
42. 10.1016/S1381-1169(01)00246-110.1016/S1381-1169(01)00246-1 ↗
43. 10.1021/ja805616610.1021/ja8056166 ↗
44. 10.1021/jo010217r10.1021/jo010217r ↗
45. 10.1002/anie.20150374110.1002/anie.201503741 ↗
46. 10.1021/ja508679h10.1021/ja508679h ↗
47. 10.1038/nature0165010.1038/nature01650 ↗
48. 10.1039/B618320B10.1039/B618320B ↗
49. 10.1038/nchem.44410.1038/nchem.444 ↗
50. 10.1021/ar100061710.1021/ar1000617 ↗
51. 10.1039/c3ce41232f10.1039/c3ce41232f ↗
52. 10.1038/nchem.83410.1038/nchem.834 ↗
53. 10.1021/ja512973b10.1021/ja512973b ↗
54. 10.1126/science.119216010.1126/science.1192160 ↗
55. 10.1039/c4cc00113c10.1039/c4cc00113c ↗
56. 10.1021/cr400647310.1021/cr4006473 ↗
57. 10.1002/anie.20120447510.1002/anie.201204475 ↗
58. 10.1021/ic300825s10.1021/ic300825s ↗
59. 10.1021/ja405082810.1021/ja4050828 ↗
60. 10.1039/C5DT01421B10.1039/C5DT01421B ↗
61. 10.1021/ja511131710.1021/ja5111317 ↗
62. 10.1002/chem.20140289510.1002/chem.201402895 ↗
63. 10.1021/ja510525s10.1021/ja510525s ↗
64. 10.1002/(SICI)1521-3765(19981102)4:11<2299::AID-CHEM2299>3.0.CO;2-H10.1002/(SICI)1521-3765(19981102)4:11<2299::AID-CHEM2299>3.0.CO;2-H ↗