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- Impact of intrinsic framework flexibility for selective adsorption of sarin in non-aqueous solvents using metal–organic frameworks. Jongwoo Park, Mayank Agrawal, Dorina F. Sava Gallis, Jacob A. Harvey, Jeffery A. Greathouse, David S. Sholl
, Phys. Chem. Chem. Phys.
, 2020
, 22
, 6441
- Impact of ambient gases on the mechanism of [Cs8Nb6O19]-promoted nerve-agent decomposition. Alexey L. Kaledin, Darren M. Driscoll, Diego Troya, Daniel L. Collins-Wildman, Craig L. Hill, John R. Morris, Djamaladdin G. Musaev
, Chem. Sci.
, 2018
, 9
, 2147
- Theoretical studies of reaction pathways and energy barriers for alkaline hydrolysis of phosphotriesterase substrates paraoxon and related toxic phosphofluoridate nerve agents. Fang Zheng, Chang-Guo Zhan, Rick L. Ornstein
, J. Chem. Soc., Perkin Trans. 2
, 2001
, 2355
- Thermal separation to facilitate Direct Analysis in Real Time (DART) of mixtures. J. Michael Nilles, Theresa R. Connell, H. Dupont Durst
, Analyst
, 2010
, 135
, 883
- A lab-on-a-chip for detection of nerve agent sarin in blood. Hsih Yin Tan, Weng Keong Loke, Yong Teng Tan, Nam-Trung Nguyen
, Lab Chip
, 2008
, 8
, 885
- Janus gas: reversible redox transition of Sarin enables its selective detection by an ethanol modified nanoporous SnO2 chemiresistor. Zhengfei Dai, Guotao Duan, Zhenxing Cheng, Lei Xu, Tie Li, Guangqiang Liu, Hongwen Zhang, Yue Li, Weiping Cai
, Chem. Commun.
, 2015
, 51
, 8193
- Screening of carbonaceous nanoporous materials for capture of nerve agents. Piotr Kowalczyk, Piotr A. Gauden, Artur P. Terzyk, Alexander V. Neimark
, Phys. Chem. Chem. Phys.
, 2013
, 15
, 291
- Is it possible to reverse aged acetylcholinesterase inhibited by organophosphorus compounds? Insight from the theoretical study. Yun An, Yali Zhu, Yuan Yao, Junjun Liu
, Phys. Chem. Chem. Phys.
, 2016
, 18
, 9838
- 756. The reaction of oximes with isopropyl methylphosphono-fluoridate (Sarin). A. L. Green, B. Saville
, J. Chem. Soc.
, 1956
, 3887
- Stability of N-heterocyclic oxime derivatives. Part V. Kinetics of the reaction of 2-hydroxyiminomethyl-1-methylpyridinium iodide and isopropyl methylphosphonofluoridate in water at 15, 25, and 35° and at pH 5·7–7·7. J. H. Blanch
, J. Chem. Soc. B
, 1969
, 1172