Asymmetric Oxygen Bridged Copper(II) Carboxylate: Synthesis, Complete Characterization, and Crystal Structure

Abstract

Binuclear centrosymmetric copper(II) complex of the formula bipyCu(L)4Cubipy, where bipy = 2,2′- bipyridine and L = 4-methoxy-2-phenyl acetate, is synthesized and characterized by FT-IR, UV-Visible, ESR and mass spectroscopy, electrochemical, thermogravimetric, and single crystal XRD techniques. The complex contains two differently oriented molecules per unit cell stabilized via intermolecular interactions. Geometry around each Cu(II) was found to be square pyramidal affected by asymmetrically bridging oxygen atoms occupying the apical position of one square pyramid and the axial position of another in the same binuclear molecule. The square base is formed by two oxygen atoms from two carboxylate ligands and two nitrogen atoms from the bipyridine moiety. TGA shows that the complex is stable up to 170 °C followed by stepwise loss of coordinated ligands, which was supported by GC-MS data as well. A broad absorption spectrum indicated 2B1g as the ground state and single electron occupancy of the dx2–y2 orbital, which was confirmed by the ESR spectrum. The electrochemical study gives two oxidation curves corresponding to Cu(II)/Cu(III) and Cu(I)/Cu(II) and a reduction signal corresponding to the Cu(II)/Cu(I) process. The robust complex represents an interesting contribution to the understanding of coordination chemistry.