Thermal Response, Catalytic Activity, and Color Change of the First Hybrid Vanadate Containing Bpe Guest Molecules
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- 作者：Roberto Fern谩ndez de Luis ; M. Karmele Urtiaga ; Jos茅 L. Mesa ; Edurne S. Larrea ; Marta Iglesias ; Te贸filo Rojo ; Mar铆a I. Arriortua
- 刊名：Inorganic Chemistry
- 出版年：2013
- 出版时间：March 4, 2013
- 年：2013
- 卷：52
- 期：5
- 页码：2615-2626
- 全文大小：650K
- 年卷期：v.52,no.5(March 4, 2013)
- ISSN：1520-510X
文摘
Four isomorphic compounds with formula [{Co2(H2O)2(Bpe)2}(V4O12)]路4H2O路Bpe, CoBpe 1; [{CoNi(H2O)2(Bpe)2}(V4O12)]路4H2O路Bpe, CoNiBpe 2; [{Co0.6Ni1.4(H2O)2(Bpe)2}(V4O12)]路4H2O路Bpe, NiCoBpe 3; and [{Ni2(H2O)2(Bpe)2}(V4O12)]路4H2O路Bpe, NiBpe 4, have been obtained by hydrothermal synthesis. The crystal structures of CoBpe 1 and NiBpe 4 were determined by single-crystal X-ray diffraction (XRD). The Rietveld refinement of CoNiBpe 2 and NiCoBpe 3 XRD patterns confirms that those are isomorphic. The compounds crystallize in the P1̅ space group, exhibiting a crystal structure constructed from inorganic layers pillared by Bpe ligands. The crystal structure contains intralayer and interlayer channels, in which the crystallization water molecules and Bpe guest molecules, respectively, are located. The solvent molecules establish a hydrogen bonding network with the coordinated water molecules. Thermodiffractometric and thermogravimetric studies showed that the loss of crystallization and coordinated water molecules takes place at different temperatures, giving rise to crystal structure transformations that involve important reduction of the interlayer distance, and strong reduction of crystallinity. The IR, Raman, and UV鈥搗is spectra of the as-synthesized and heated compounds confirm that the structural building blocks and octahedral coordination environment of the metal centers are maintained after the structural transformations. The color change and reversibility of the water molecules uptake/removal were tested showing that the initial color is not completely recovered when the compounds are heated at temperatures higher than 200 掳C. The thermal evolution of the magnetic susceptibility indicates one-dimensional antiferromagnetic coupling of the metal centers at high temperatures. For NiCoBpe 3 and NiBpe 4 compounds magnetic ordering is established at low temperatures, as can be judged by the maxima observed in the magnetic susceptibilities. CoNiBpe 2 was proved as catalyst being active for cyanosilylation reactions of aldehydes.