Crystal structures of three anhydrous nitroprussides: M†Fe„CN…5NO‡ „M=Mn,Zn,Cd…
The crystal structures of Mn, Zn, and Cd nitroprussides in their anhydrous state, M Fe CN 5NO M=Mn,Zn,Cd , were refined from XRD powder patterns using the Rietveld method. These compounds have a porous framework useful for adsorption and storage of small molecules. Water crystallization can be remov...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2006 |
| País: | México |
| Institución: | Instituto Politécnico Nacional |
| Repositorio: | Repositorio Digital del IPN |
| OAI Identifier: | oai:www.repositoriodigital.ipn.mx:123456789/11199 |
| Acceso en línea: | http://hdl.handle.net/123456789/712 http://www.repositoriodigital.ipn.mx/handle/123456789/11199 |
| Access Level: | acceso abierto |
| Palabra clave: | nitroprusside porous material Rietveld crystal structure Prussian blue analogues |
| Sumario: | The crystal structures of Mn, Zn, and Cd nitroprussides in their anhydrous state, M Fe CN 5NO M=Mn,Zn,Cd , were refined from XRD powder patterns using the Rietveld method. These compounds have a porous framework useful for adsorption and storage of small molecules. Water crystallization can be removed by heating below 100 °C without disrupting the 3D network by introducing certain structural modification mainly around the M site Mn, Zn, Cd . For M=Mn and Cd, the compounds were found to be orthorhombic with space group Pnma Mn:a=13.7844 1 , b=7.3750 2 , c=10.9470 2 Å, V=1112.8 1 Å3, Z=4; Cd:a=13.9566 3 , b=7.5040 4 , c =11.0230 2 Å, V=1154.4 1 Å3, Z=4 . Anhydrous zinc nitroprusside crystallizes in rhombohedral with space group R3¯ a=b=19.2525 1 ,c=17.7107 2 Å, =120.0° ,V=5685.1 1 Å3 ,Z=18 . When exposed to humid air, these anhydrous compounds become hydrated. The XRD powder patterns were recorded under vacuum on samples dehydrated in situ. The structural information from XRD was complemented with thermo-gravimetric, infrared, and Mössbauer data. © 2007 International Centre for Diffraction Data. DOI: 10.1154/1.2434787 |
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