Self-Process-Programmed Structural Diversity in Supramolecular Assembly Based on Polyoxometalate Anion and Halogensubstituted Bipyridine Cation

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• 作者：Zhangang Han ; Yuanzhe Gao ; Xueliang Zhai ; Jun Peng ; Aixiang Tian ; Yulong Zhao ; Changwen Hu
• 刊名：Crystal Growth & Design
• 出版年：2009
• 出版时间：February 4, 2009
• 年：2009
• 卷：9
• 期：2
• 页码：1225-1234
• 全文大小：628K
• 年卷期：v.9,no.2(February 4, 2009)
• ISSN：1528-7505

文摘

To investigate the relationship between network connectivity and the types of anions and cations, we synthesized a series of supramolecular assemblies based on different polyoxometalate (POM) anions and halogen-substituted bipyridine cations, namely, (Hcpy)₆H₂[PMo₁₂O₄₀] (1), (Hcpy)₃[PMo₁₂O₄₀]·2.2H₂O (2), (Hcpy)₂(Hbppy)₂[PMo₁₂O₄₀]·2H₂O (3), (Hcpy)₂(Hbppy)H₂[PMo₁₂O₄₀]·H₂O (4), (Hbppy)₄[GeW₁₂O₄₀]·3H₂O (5), (Hbppy)₄[β-Mo₈O₂₆] (6), and (H_6/7bppy)₇[P₂W₁₈O₆₀]·5H₂O (7) (cpy = 4-(5-chloropyridin-2-yl)pyridine and bppy = 4-(5-(4-bromophenyl)pyridin-2-yl)pyridine). These compounds have been structurally characterized by elemental analyses, IR spectra, thermogravimatric analysis, and X-ray crystallography. All supramolecular frameworks of 1−7 are guided by nonconvalent interactions, especially directional hydrogen bonds and halogen bonds. Research results reveal that decorating nitrogen heterocycles with inductive electron withdrawal halogen groups increases the tendency to form face-to-face π-stacking interactions between them. Anionic clusters also present different and interesting structural features: in 1 and 5 Keggin-type anions form a one-dimensional pillar-like structure, while forming a two-dimensional waved sheet in 4, and only isolated clusters in 2 and 3. Compounds 1−5 consist of Keggin-type clusters with different organic cpy and bppy cations. Complex 6 is a supramolecular assembly based on [β-Mo₈O₂₆]⁴⁻ and bppy, whereas complex 7 is an assembly containing Dawson-type clusters in which anions allow the assembly of bppy cations into distorted-wave organic layers. These results show that the types and ratios of cations and anions play significant roles in fabricating inorganic−organic arrangements. The thermal and electrochemistry properties of these compounds are discussed.