摘要
The reaction of trivacant Keegin germanotungstate [A-α-GeW 9O34]10- with Mn2+ and Ce 4+ cations in the presence of oxalate ligand under hydrothermal conditions led to the isolation of a novel organic-inorganic hybrid 3d-4f heterometallic germanotungstate K4Na4[Ce 2(ox)3(H2O)2]2{[Mn(H 2O)3]2[Mn4(GeW9O 34)2(H2O)2]·14H2O (1) (ox = oxalate), which has been characterized by elemental analysis, IR spectroscopy, thermogravimetric (TG) analysis, and single-crystal X-ray crystallography. Interestingly, each tetra-MnII-substituted sandwich-type unit acts as 14-dentate ligands to link eight Ce3+ centers and six Mn2+ centers further into a three-dimensional (3D) architecture. The 3D structure can be considered as two parts: one is the two-dimensional layer formed by sandwich-type [Mn4(H 2O)2(GeW9O34)2] 12- fragments and Mn2+ linkers; the other layer is constructed from Ce3+ cations and oxalate bridges, and the two layers are combined together alternately through W-O-Ce-O-W linkers, resulting in the 3D framework. Notably, 1 exhibits the first 3d-4f 3D organic-inorganic hybrid framework constructed by sandwich-type TM-substituted polyoxoanions and mixed 3d and 4f metal linkers in POM chemistry.
源语言 | 英语 |
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页(从-至) | 5169-5174 |
页数 | 6 |
期刊 | Crystal Growth and Design |
卷 | 13 |
期 | 12 |
DOI | |
出版状态 | 已出版 - 4 12月 2013 |