小型商用车
化学
钍
卟啉
二甲基甲酰胺
催化作用
水溶液
连接器
金属有机骨架
金属
结晶学
组合化学
铀
光化学
有机化学
吸附
操作系统
冶金
材料科学
计算机科学
溶剂
作者
Peng Li,Subhadip Goswami,Ken‐ichi Otake,Xingjie Wang,Zhijie Chen,Sylvia L. Hanna,Omar K. Farha
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2019-02-25
卷期号:58 (6): 3586-3590
被引量:39
标识
DOI:10.1021/acs.inorgchem.8b03511
摘要
The crystal structures of thorium clusters are important for understanding the formation and transformation mechanisms of actinide species in solution, which can in turns benefit nuclear waste processing and management. However, stabilizing thorium clusters in aqueous solution is quite challenging because of their fast olation and oxolation reactions. Here, we report a thorium-based metal-organic framework, NU-905, with the formula [Th6(μ3-O)2(HCOO)4(H2O)6(TCPP)4] [TCPP = tetrakis(4-carboxyphenyl)porphyrin], synthesized by a solvothermal reaction in N, N-dimethylformamide and water at 120 °C. NU-905 contains a hexanuclear secondary building unit (SBU), [Th6(μ3-O)2(HCOO)4(H2O)6], which has never been reported previously. The SBUs are capped and bridged by the tetratopic linker TCPP to form a three-dimensional network with scu topology. The activated NU-905 exhibits permanent porosity and shows high catalytic activity for the selective photooxidation of a mustard gas simulant.
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