Abstract
Eighteen mononuclear diorganotin(IV) complexes derived from tridentate Schiff bases and R2SnO (IV) oxides (R = Me, n-Bu, Ph) were synthetized by multicomponent reactions in moderate yields. Complexes were characterized by common spectroscopic techniques such as FT-IR, UV–vis, mass spectrometry and NMR (1H, 13C and 119Sn) spectroscopy analysis. Nine complexes were characterized by single crystal X-ray diffraction analysis (1c, 1d, 1g, 1k, 1n, 1o, 1p, 1q and 1r). 119Sn NMR spectra showed signals at δ = 135–145, 175–185 and 319–323 ppm for Me, n-Bu and Ph derivatives respectively, indicating the pentacoordination of the tin atoms. In solid state, for compounds 1c, 1d, and 1g a distorted octahedral geometry for tin atoms was observed owing the presence of intermolecular Sn⋯O interactions, while for compounds 1k, 1n-1r, the pentacoordinate environment for tin atoms is observed. At supramolecular level the presence of OH⋯O, CH⋯O, CH⋯X (X = Cl, Br), CH⋯π and π⋯π interactions allow the formation of 1D and 2D polymeric chains.
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