Synthesis and Fluorescence Properties of Structurally Characterized Heterobimetalic Cu(II)–Na(I) Bis(salamo)-Based Complex Bearing Square Planar, Square Pyramid and Triangular Prism Geometries of Metal Centers

A novel heterotrinuclear complex [Cu(2)(L)Na(µ-NO(3))]∙CH(3)OH∙CHCl(3) derived from a symmetric bis(salamo)-type tetraoxime H(4)L having a naphthalenediol unit, was prepared and structurally characterized via means of elemental analyses, UV-Vis, FT-IR, fluorescent spectra and single-crystal X-ray diffraction. The heterobimetallic Cu(II)–Na(I) complex was acquired via the reaction of H(4)L with 2 equivalents of Cu(NO(3))(2)·2H(2)O and 1 equivalent of NaOAc. Clearly, the heterotrinuclear Cu(II)–Na(I) complex has a 1:2:1 ligand-to-metal (Cu(II) and Na(I)) ratio. X-ray diffraction results exhibited the different geometric behaviors of the Na(I) and Cu(II) atoms in the heterotrinuclear complex; the both Cu(II) atoms are sited in the N(2)O(2) coordination environments of fully deprotonated (L)(4−) unit. One Cu(II) atom (Cu1) is five-coordinated and possesses a geometry of slightly distorted square pyramid, while another Cu(II) atom (Cu2) is four-coordination possessing a square planar coordination geometry. Moreover, the Na(I) atom is in the O(6) cavity and adopts seven-coordination with a geometry of slightly distorted single triangular prism. In addition, there are abundant supramolecular interactions in the Cu(II)–Na(I) complex. The fluorescence spectra showed the Cu(II)–Na(I) complex possesses a significant fluorescent quenching and exhibited a hypsochromic-shift compared with the ligand H(4)L.