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Synthesis, molecular structure, and spectral analysis of copper(II) complexes derived from pyridinediols

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Version 5 2015-03-07, 14:27
Version 4 2015-03-07, 14:27
Version 3 2014-12-16, 23:43
Version 2 2014-11-21, 09:02
Version 1 2015-01-17, 00:00
journal contribution
posted on 2015-03-07, 14:27 authored by Guillermo M. Chans, Elizabeth Gómez, Virginia Gómez-Vidales, R. Alfredo Toscano, Cecilio Álvarez-Toledano

A series of mononuclear copper(II) complexes was synthesized by reaction of different 2,6-disubstituted pyridines with elemental Cu in a CCl4/DMSO solvent system. Physical properties were analyzed using IR, optical spectroscopy, mass spectrometry, and EPR. Single-crystal X-ray diffraction for complexes 2a and 4a revealed that the molecular structure of 2a is composed of a six-coordinate unit in which two ligands are linked to Cu(II) by oxygen and nitrogen donors. Conversely, in the molecular structure of 4a, the Cu(II) has a slightly distorted trigonal bipyramidal arrangement, where the coordination environment around the copper ion is five-coordinate. EPR spectra of Cu(II) complexes were illustrated elaborately and some theoretical data were abstracted from EPR curves to support the proposed structures.

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