Grid-type complexes of M2+ (M=Co, Ni, and Zn) with highly soluble bis(hydrazone)thiopyrimidine-based ligands: Spectroscopy and electrochemical properties

• Published in: Inorganica Chimica Acta Vol. 468; pp. 131 - 139
• Main Authors: Carmona-Vargas, Christian C., Váquiro, Ingri Y., Jaramillo-Gómez, Luz M., Lehn, Jean-Marie, Chaur, Manuel N.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.11.2017
• Subjects: Hydrazones; Metallogrids; Supramolecular chemistry; Hydrazones; Metallogrids; Supramolecular chemistry
• ISSN: 0020-1693; 1873-3255
• DOI: 10.1016/j.ica.2017.05.002

[Display omitted] •Grid complexes with tridentate bis(hydrazone)thiopyrimidine-based ligands were obtained.•Highly soluble metal complexes are reported.•Cobalt (II) complexes, exhibited a richer electrochemistry with a larger number of redox processes. Herein we present the syntheses of two types of two-site symmetric bis(hydrazone) ligands (1 and 2) which contain two tridentate subunits suitable for metal ion complexation, with remarkable solubility in most organic solvents, contrary to other pyrimidine-based bis(hydrazones) used for the preparation of metallogrids. As expected, compounds 1 and 2 exhibit conformational changes when coordinated metal ions (Zn2+, Ni2+, Co2+) through the two terpyridine-like sites leading to the metal complexes 1a–c and 2a–c. The absorption spectra and redox properties of ligands 1 and 2 and of the metal complexes 1a–c and 2a–c were studied. Compounds 1 and 2 exhibit absorption spectra dominated by intense π–π∗ bands in the UV region, while the absorption spectra of the metal complexes 1a–c and 2a–c show intense bands in the UV region, due to the spin-allowed ligand-centred (LC) transitions, and in the visible region, due to spin-allowed metal-to-ligand charge transfer (MLCT) transitions. Cyclic voltammetry and square wave voltammetry were carried out in order to establish the relevance of the complexation, and the grid formation in the redox potentials of the ligands 1 and 2.