类金刚石
吸附
金属有机骨架
羧酸盐
化学
溶剂
环己酮
溶剂热合成
无机化学
齿合度
红外光谱学
苯
有机化学
金属
吸附
分子
催化作用
作者
Gift Mehlana,G. Ramon,Susan A. Bourne
标识
DOI:10.1016/j.micromeso.2016.05.016
摘要
The characterisation of a 4-fold interpenetrated diamondoid metal-organic framework (MOF) {[Ni4(44pba)8]·sol}n, (1) (44pba = 4-(4-pyridyl)benzoate) is reported. The compound was prepared from Ni(II) and 44pba under solvothermal conditions. When activated to give 1d, the compound absorbs a wide range of solvents which is accompanied by a visible colour change. Sorption of water triggers an irreversible phase transformation, while adsorption of methanol, ethanol, benzene, dimethylformamide and cyclohexanone does not affect the structural integrity of the framework as revealed by powder X-ray diffraction studies. Apart from ethanol, the uptake of polar protic solvents gave rise to an increase in the energy difference between the asymmetric and symmetric carboxylate stretches as confirmed by infrared studies. We attributed this to a change in the binding mode of the carboxylates from chelating to monodentate. The activated phase (1d) was found to absorb high levels of iodine into its channels in comparison to other reported MOFs. This is due to the high porosity of the network compound in which aromatic walls allow for the interaction of iodine molecules with the framework walls.
科研通智能强力驱动
Strongly Powered by AbleSci AI