Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 1Citation - Scopus: 1Hydrothermal Synthesis, Characterization and Catalytic Activities of a Keggin Structure of (4,4′-Bpyh2)3[pw12o40]2•3h2o and a Wells-Dawson Structure of (4,4′-Bpyh2)3(4,4′(Elsevier, 2025) Ece, Ozlem; Chilufya, Langson; McMillen, Colin D.; Emirdag-Eanes, MehtapTwo novel polyoxometalates composed of heteropolytungstates, (4,4 '-bpyH2)3[PW12O40]2 center dot 3H2O (1) and (4,4 '- bpyH2)3(4,4 '-bpyH)1.75[Cu(bpy)2]0.25[H2P2W18O62]2 (2) have been synthesized under hydrothermal conditions and characterized by single crystal X-ray diffraction and TGA methods. Compound 1 crystallizes in the cubic space group Ia-3with a = 25.9356(12) angstrom, b = 25.936(3) angstrom, c = 25.936(3) angstrom, alpha = 90.00, (3= 90.00, gamma= 90.00 and Z = 8, and compound 2 crystallizes in the triclinic space group P-1with a = 13.5194(17) angstrom, b = 22.400(3) angstrom, c = 27.374(4) angstrom, alpha = 79.833(3), (3= 77.439(3), gamma= 80.213(4) and Z = 2. In addition to structural characterization, the catalytic activities of 1 and 2 were determined in hydrolysis reactions. In the catalytic study, starch hydrolysis reactions were performed by using hydrothermal synthesis, and starch was hydrolyzed successfully at 150 degrees C, 5 h, based on the results of Lugol's test, which highest conversion yields above 90 wt.% under optimum reaction conditions. FT-IR analysis and catalyst reusability tests were also performed for each compound. No appreciable loss was observed in activity after five reaction cycles.Article Citation - WoS: 5Citation - Scopus: 5Hydrothermal Synthesis and Characterization of One Dimensional Chain Structures of Monolacunary Keggin Polyoxoanions Substituted With Copper(Elsevier Ltd., 2015) Eanes, Mehtap; Önen, Banu; McMillen, Colin D.Two novel polymeric polyoxometallates constructed from transition metal substituted heteropolytungstates, [(4,4’bpyH2)2(4,4’bpyH)][PCuW11O39]·H2O (1), and [(4,4’bpyH2)(pyH)3][PCuW11O39]·2H2O (2), (4,4’bpy = 4,4’bipyridine, py = pyridine) have been synthesized under hydrothermal conditions and characterized by IR, TGA, single crystal X-ray diffraction and magnetic measurements. The product formation showed a high sensitivity toward experimental factors including pH and stirring. Compounds 1 crystallizes in the monoclinic space group P2(1)/n with a = 13.503(3) Å, b = 26.726(5) Å, c = 15.168(3) Å, = 99.61(3)° and Z=4. The second compound also crystallizes in space group P2(1)/n, but with a = 13.519(3) Å, b = 20.431(4) Å, c =18.655(4) Å, = 96.52(3)° and Z=4. Compound 1 exhibits a zigzag chain structure, while compound 2 exhibits a straight chain structure. Compound 2 is the first example of a polyoxometallate containing 1D chains of transitionmetal- substituted heteropolytungstate designed with two significantly different organic units as the countercations. The Cu2+ ions in 1 exhibit paramagnetic behavior.
