Abstract
The first study of the self-association of a copper(I) tetrahedral complex ([Cu(N-{4-nitrophenyl}pyridine-2-yl-methanimine)(PPh3)Br]) has been performed. The formation of a discrete dimer supported by supramolecular π-π stacking and C-H·Br interactions was established by X-ray diffraction techniques. 1D- and 2D NMR techniques were used for the structural characterization of this compound in solution. Unexpected 1H- 1H NOE effects are coherent with the presence of a dimer in solution, whose structure replicates that found in the crystal. Dimerization constants obtained by VT-1H NMR spectroscopy allowed the determination ofthe thermodynamic parameters for the self-association process, namely ΔS = -0.67±0.21 calmol-1K-1, ΔH = -2.00±0.05 kcalmol-1 and ΔG(298 K) = -1.79 kcalmol -1. Consequently, this association process is enthalpy driven. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Jara, D. H., Lemus, L., Farías, L., Freire, E., Baggio, R., & Guerrero, J. (2012). Spectroscopic evidence in solid and solution of a discrete copper(I) tetrahedral complex dimer supported by supramolecular interactions. European Journal of Inorganic Chemistry, (10), 1579–1583. https://doi.org/10.1002/ejic.201101356
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