化学
沸石咪唑盐骨架
水解
咪唑酯
微晶
锌
氢键
化学工程
水溶液
傅里叶变换红外光谱
结晶学
无机化学
金属有机骨架
分子
有机化学
吸附
工程类
作者
Huifeng Zhang,Man Zhao,Yang Yang,Y. S. Lin
标识
DOI:10.1016/j.micromeso.2019.109568
摘要
Recent studies have shown that zeolitic imidazolate framework-8 (ZIF-8) crystallites are not stable in aqueous solution under ambient conditions. When immersed in water, ZIF-8 crystallites are hydrolyzed to zinc and imidazolate ions, which can be condensed to form a new solid substance upon removal of water by evaporation. The present work demonstrates such ZIF-8 phase shift substance is of crystalline structure but does not belong to any known (pseudo)polymorphs of ZIF-8, ZIF-L, dia(Zn), or decomposed product of ZIF-8: Zn(OH)2 and 2-methylimidazole. FTIR characterization shows the co-existence of Zn–O and Zn–N bond in the new substance, confirming the partial cleavage of Zn–N bond in ZIF-8 building unit in the hydrolysis step. EDS quantification for the ZIF-8 phase shift substance gives a C:N:Zn:O atomic ratio of 40:20:5:4. Based on EDS and FTIR results, the chemical formula of Zn5(HMIM)4(MIM)6(OH)4 for the building unit of such substance is proposed consisting of four partially hydrolyzed and one undisturbed secondary ZIF-8 building units. The ZIF-8 phase shift substance is crystalline with a nearly identical atomic composition as ZIF-8 (except for increased oxygen content), suggesting it might be a novel pseudo-polymorph of ZIF-8. The hydrolysis and condensation of ZIF-8 can be described by a mechanism that includes (1) hydrolysis of ZIF-8 through cleavage of Zn–N bond to form zinc and imidazolate ions and partially hydrolyzed ZIF-8 units and (2) condensation of these ions and clusters with the help of hydrogen bond to form the new structure of ZIF-8 phase shift substance.
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