Abstract
A new polyoxomolybdate, [(C6H12N4-CH3)2Na2(H2O)8](C6H12N4-CH3)2[(H0.5)N(CH2O)3FeMo6O18.5(OH)2.5]2·10H2O (1), was synthesized. The structure of the synthesized polyoxomolybdate was investigated by single-crystal X-ray diffraction analysis and several other identification techniques such as FTIR and EDX analysis. Each unit cell of 1 contains one cation [(C6H12N4-CH3)2Na2(H2O)8]4+ and two hexamethylenetetramine cations (C6H12N4-CH3)+, and two polyanions [(H0.5)N(CH2O)3FeMo6O18.5(OH)2.5]3– with ten water molecules in the crystal lattice. In the polyanion, molybdenum ions are bonded to two terminal oxygen atoms and two μ2- (Mo-Mo) and μ3- (Mo-Fe-Mo) bridging oxygen atoms. Iron in the center of the polyanion 1 is also surrounded by three deprotonated oxygens of trimethanolamine ligand and three μ3- (Mo-Fe-Mo) bridging oxygen atoms. This new polyoxomolybdate was used as an efficient catalyst in the azide–alkyne cycloaddition reaction to produce various 1,2,3-triazoles with high yields. Additional investigations reveal this catalytic system can be refreshed and utilized for up to six successive applications.
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