Abstract
A new organic-inorganic compound based on octamolybdate building blocks and copper(II) complexes of tetradentate N-donor ligands has been hydrothermally synthesized, namely [Cu(cyclam)]2[Mo8O26]·1.5H2O (1), (cyclam: 1,4,8,11–tetraazacyclotetradecane). Compound 1 has been chemically (elemental and thermal analyses), spectroscopically (infrared spectroscopy), and structurally (single crystal and powder X-ray diffraction) characterized. The crystal packing of 1 shows a covalent framework structure formed by [Mo8O26]n4n− chains running along the 100 direction which are linked to each other through the coordination spheres of {Cu(cyclam)}2+ complexes leading to a three-dimensional open network. This structural assembly generates voids that can be described as a succession of cavities communicated through narrow bottlenecks with approximate cross section of 4 × 7 Å2 where the hydration water molecules are hosted. The robust open structure of 1 remains virtually unaltered upon thermal evacuation of guest solvent molecules at 130 °C, resulting in the anhydrous phase [Cu(cyclam)]2[Mo8O26] (1a) with potentially accessible micropores as demonstrated by single-crystal X-ray diffraction measurements. Electron paramagnetic resonance spectroscopy analysis of 1 has also been assessed.
Highlights
Porous crystalline materials such as metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) are of great interest due to their wide range of applications related to their permanent porous nature [1,2,3,4,5].the former field has entered a new stage where the porosity and other physical properties are playing a key role in their potential application in current fields of interest like catalysis, magnetism or biomedicine [6,7,8,9,10]
Recent work in MOF-chemistry have shown that small pores and the use of small inorganic oxoanions with electronegative atoms like oxygen pointing at the interior of the cavities, improve the selectivity of coordination frameworks towards small polarizable molecules like CO2 [11,12,13]
The synthetic approach could be extended to larger oxo-units, the crystal packing of which leads to relatively small pores within the structure
Summary
Departamento de Química Inorgánica, Facultad de Ciencia y Tecnología, Universidad del País Vasco. Laboratoire des Matériaux et Cristallochimie, Institut Supérieur des Sciences Appliquées et Technologie, 5111 Mahdia, Tunisia
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