Porous, rigid metal(III)-carboxylate metal-organic frameworks for the delivery of nitric oxide

被引:63
|
作者
Eubank, Jarrod F. [1 ]
Wheatley, Paul S. [2 ]
Lebars, Gaelle [3 ]
McKinlay, Alistair C. [2 ]
Leclerc, Herve [3 ]
Horcajada, Patricia [1 ]
Daturi, Marco [3 ]
Vimont, Alexandre [3 ]
Morris, Russell E. [2 ]
Serre, Christian [1 ]
机构
[1] Univ Versailles St Quentin En Yvelines, Inst Lavoisier, UMR CNRS 8180, F-78035 Versailles, France
[2] Univ St Andrews, EaStChem Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[3] Univ Caen, ENSICAEN, CNRS, Lab Catalyse & Spectrochim, F-14050 Caen, France
来源
APL MATERIALS | 2014年 / 2卷 / 12期
关键词
HYDROGEN STORAGE; MIL-100(FE); MOF; SEPARATION; CHEMISTRY; SORPTION; ANEMIA; SITES; PORES; NO;
D O I
10.1063/1.4904069
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The room temperature sorption properties of the biological gas nitric oxide (NO) have been investigated on the highly porous and rigid iron or chromium carboxylate based metal-organic frameworks Material Institut Lavoisier (MIL)-100(Fe or Cr) and MIL-127(Fe). In all cases, a significant amount of NO is chemisorbed at 298 K with a loading capacity that depends both on the nature of the metal cation, the structure and the presence of additional iron(II) Lewis acid sites. In a second step, the release of NO triggered by wet nitrogen gas has been studied by chemiluminescence and indicates that only a partial release of NO occurs as well as a prolonged delivery at the biological level. Finally, an in situ infrared spectroscopy study confirms not only the coordination of NO over the Lewis acid sites and the stronger binding of NO on the additional iron(II) sites, providing further insights over the partial release of NO only in the presence of water at room temperature. (C) 2014 Author(s).
引用
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页数:10
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