微型多孔材料
热重分析
催化作用
等结构
粉末衍射
金属有机骨架
二甲基乙酰胺
化学
路易斯酸
无机化学
苯乙烯氧化物
材料科学
晶体结构
结晶学
有机化学
苯乙烯
吸附
溶剂
聚合物
共聚物
作者
Shyam Biswas,M. Maes,Amarajothi Dhakshinamoorthy,Mark Feyand,Dirk De Vos,Hermenegildo Garcı́a,Norbert Stock
摘要
Two isostructural microporous metal–organic frameworks [Co(DMA)6]3[(Co4Cl)3(BTT)8(H2O)12]2·12H2O (BTT3− = 1,3,5-benzenetristetrazolate; DMA = N,N′-dimethylacetamide) (1) and [Cd(DMF)6]3[(Cd4Cl)3(BTT)8(H2O)12]2·14H2O·4DMF (DMF = N,N′-dimethylformamide) (2) were synthesized under solvothermal conditions. The structures of both compounds were determined by single-crystal X-ray diffraction data. Each compound adopts a porous three-dimensional framework consisting of square-planar [M4Cl]7+ (M2+ = Co, 1; Cd, 2) units interconnected by triangular tritopic BTT3− bridging ligands to give an anionic (3,8)-connected “Moravia” net. Phase purity of the compounds was confirmed by X-ray powder diffraction (XRPD), IR spectroscopy, thermogravimetric (TG) and elemental analysis. TGA and temperature-dependent XRPD (TDXRPD) experiments indicate a moderate thermal stability up to 350 and 300 °C, respectively. Guest exchange followed by heating led to microporous solids with coordinatively unsaturated metal sites. These unsaturated metal sites create opportunities in adsorptive and catalytic applications. These have been probed by the selective removal of sulfur compounds from fuel feeds as well as the catalytic ring opening of styrene oxide and the oxidation of several cycloalkanes and benzyl compounds.
科研通智能强力驱动
Strongly Powered by AbleSci AI