1D Polyoxometalate-Based Composite Compounds Derived from the Wells−Dawson Subunit:  Synthesis and Crystal Structure of [{Ce(DMF)4(H2O)3}{Ce(DMF)4(H2O)4}(P2W18O62)]·H2O and [{La(DMF)6(H2O)}{La(DMF)4.5(H2O)2.5}(P2W18O62)]

• Published in: Crystal growth & design 2004-03, Vol.4 (2), p.241-247
• Main Authors: Niu, Jing-Yang, Guo, Dong-Jie, Wang, Jing-Ping, Zhao, Jun-Wei
• Format: Article
• Language: English
• Subjects: Condensed matter: structure, mechanical and thermal properties; Exact sciences and technology; Heterocyclic compounds; Inorganic compounds; Metal complexes; Organic compounds; Physics; Structure of solids and liquids; crystallography; Structure of specific crystalline solids
• ISSN: 1528-7483; 1528-7505
• DOI: 10.1021/cg034131y

Two composite compounds, [{Ce(DMF)4(H2O)3}{Ce(DMF)4(H2O)4}(P2W18O62)]·H2O (1) (DMF = N,N-dimethylformamide) and [{La(DMF)6(H2O)}{La(DMF)4.5(H2O)2.5}·(P2W18O62)] (2), have been constructed at room temperature and characterized by single crystal X-ray structural analyses, ESR spectroscopy, and thermogravimetric (TG) and differential thermal analysis (DTA) measurements. Single crystal X-ray structural analyses reveal that the adjacent polyanions are polymerized to form a 1D infinitely linear chain by the bridging RE coordination cations and exhibit an -ACACAC- type of structure, and that two types of terminal oxygen atoms of the Wells−Dawson polyanion located in the “cap” and “belt” sites are involved in coordination with the RE3+ ions, respectively. ESR spectra indicate that after irradiation with sunlight, compound 2 forms a mixed-valence heteropoly compound with unshared electrons. From TG-DTA analyses, we surmise that the frameworks of polyanions of this kind of compound decompose at ca. 620 °C.