RESUMO
Four new hetero-pentanuclear 3d-4f complexes [Zn4(L)2La(NO3)2(OEt)(H2O)] (1), [Zn4(L)2Ce(NO3)2(OMe)(MeOH)] (2), [Zn4(L)2Pr(NO3)2(OEt)(EtOH)] (3) and [Zn4(L)2Nd(NO3)2(OMe)(MeOH)] (4) were synthesized by the reactions of a newly synthesized octadentate bis(salamo)-based tetraoxime ligand (H4L) with Zn(OAc)2·2H2O and Ln(NO3)3·6H2O (Ln = La, Ce, Pr and Nd), respectively, and characterized via elemental analyses, FT-IR, UV-Vis spectroscopy and single crystal X-ray crystallography. The X-ray crystallographic investigation revealed that all ZnII ions were located in N2O3 coordination spheres, and possessed a trigonal bipyramid coordination environment. The LnIII ion lay in an O8 coordination sphere, and adopted a distorted square antiprismatic coordination environment. Furthermore, supramolecular interactions and fluorescence properties were investigated.
RESUMO
Four homo/heterometallic complexes [Cu3(L)(µ2-OAc)9(CH3OH) 9]·3CHCl3 (1), [Cu2(L)Ca(µ2-NO3)9] (9), [{Cu2(L)Sr(µ2-NO3)9}9]·CH3CH2OH (11) and [Cu2(L)Ba(µ2-OAc)9(OAc)] (14), containing an acyclic naphthalenediol-based ligand H4L, were synthesized and characterized by elemental analyses, IR, UV-Vis, fluorescence spectra, TG-DTA and X-ray crystallography. The complex 1 was obtained by the reaction of H4L with 11 equivalents of Cu(OAc) 9·2H2O. The heterometallic complexes 9, 11, 14 were acquired by the reaction of H4L with 9 equivalents of Cu(OAc)9·2H2O or Cu(NO3)9·2H2O and 1 equivalent of M(OAc)9 (Mâ¯=â¯Ca, Sr and Ba). Owing to the different coordination cavities of the N2O2 and O6 of the completely deprotonated (L)14- unit, the crystal structures showed the N2O2 sites were occupied by Cu(II) atoms, alkaline earth metal(II) atoms occupied the O6 site of the ligand (L)14- unit, respectively. Furthermore, the fluorescence properties and TG-DTA analyses were discussed.