Anion directed template synthesis of Cu(II) complexes of a N,N,O donor mono-condensed Schiff base ligand: A molecular scaffold forming highly ordered H-bonded rectangular grids

Anion directed, template syntheses of two dinuclear copper(II) complexes of mono-condensed Schiff base ligand Hdipn (4-[(3-aminopentylimino)-methyl]-benzene-1,3-diol) involving 2,4-dihydroxybenzaldehyde and 1,3-diaminopentane were realized in the presence of bridging azide and acetate anions. Both complexes, [Cu2(dipn)2(N3)2] (1) and [Cu2(dipn)2(OAc)2] (2) have been characterized by X-ray crystallography. The two mononuclear units are joined together by basal–apical, double end-on azido bridges in complex 1 and by basal–apical, double mono-atomic acetate oxygen-bridges in 2. Both complexes form rectangular grid-like supramolecular structures via H-bonds connecting the azide or acetate anion and the p-hydroxy group of 2,4-dihydroxybenzaldehyde. Variable-temperature (300–2 K) magnetic susceptibility measurements reveal that complex 1 has antiferromagnetic coupling (J = −2.10 cm−1) through the azide bridge while 2 has intra-dimer ferromagnetic coupling through the acetate bridge and inter-dimer antiferromagnetic coupling through H-bonds (J = 2.85 cm−1, J′ = −1.08 cm−1).

Anion directed, template synthesis of two dinuclear copper(II) complexes of mono-condensed Schiff base ligand involving 2,4-dihydroxybenzaldehyde and 1,3-diaminopentane were realized in the presence of bridging azide and acetate anions. Both the complexes form rectangular grid like supramolecular structure by H-bonds. The azido bridged complex shows antiferromagnetic coupling while the acetate bridged complex shows intra-dimer ferromagnetic coupling and inter-dimer antiferromagnetic coupling.Figure optionsDownload as PowerPoint slide