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Lanthanide metal organic frameworks based on dicarboxyl-functionalized arylhydrazone of barbituric acid: syntheses, structures, luminescence and catalytic cyanosilylation of aldehydes.

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Five isostructural lanthanide MOFs, [Ln(1κOO',2κO'',3κO''',4κO''''-μ4-L)(NO3)(DMF)2]n·n(DMF) {Ln = La3+ (1), Ce3+ (2), Nd3+ (3), Sm3+ (4) and Dy3+ (5); L = 5-[2-{2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene}hydrazinyl]isophthalate; DMF = N,N'-dimethyl formamide}, based on dicarboxyl-functionalized arylhydrazone of… Click to show full abstract

Five isostructural lanthanide MOFs, [Ln(1κOO',2κO'',3κO''',4κO''''-μ4-L)(NO3)(DMF)2]n·n(DMF) {Ln = La3+ (1), Ce3+ (2), Nd3+ (3), Sm3+ (4) and Dy3+ (5); L = 5-[2-{2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene}hydrazinyl]isophthalate; DMF = N,N'-dimethyl formamide}, based on dicarboxyl-functionalized arylhydrazone of barbituric acid were synthesized under solvothermal conditions. They were characterized by elemental analysis, FT-IR spectroscopy, thermogravimetric and X-ray diffraction analyses. Crystal structure analysis revealed that these frameworks possess a similar type of two dimensional (2D) structure with a dinuclear {Ln2(COO-)2} unit acting as a secondary building block. Topological analysis shows that these frameworks display a 3,6-connected kgd; Shubnikov plane (3.6.3.6)/dual net. They exhibit excellent heterogeneous catalytic activities (compound 2 is the most active one) towards the cyanosilylation of aldehydes under solvent-free conditions. These catalysts can be recycled at least up to five cycles without a loss of activity. Compounds 1-5 exhibit luminescence properties in the solid state at room temperature.

Keywords: based dicarboxyl; arylhydrazone barbituric; barbituric acid; cyanosilylation aldehydes; functionalized arylhydrazone; dicarboxyl functionalized

Journal Title: Dalton transactions
Year Published: 2017

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