Synthesis,crystal structures and spectroscopic properties of dichloroethylphenyltin(IV) and its phenanthroline adduct |
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Authors: | Jos S. Casas,Eduardo E. Castellano,Javier Ellena,Marí a S. Garcí a‐Tasende,Agustí n S nchez,Jos Sordo,Carmen Taboada,Marí a J. Vidarte |
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Affiliation: | José S. Casas,Eduardo E. Castellano,Javier Ellena,María S. García‐Tasende,Agustín Sánchez,José Sordo,Carmen Taboada,María J. Vidarte |
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Abstract: | The reaction of dichloroethylphenyltin(IV), Ph(Et)SnCl2, with phenanthroline monohydrate (phen·H2O) in chloroform, in 1:1 mole ratio, afforded [Ph(Et)SnCl2(phen)]. The crystal structures of dichloroethylphenyltin(IV) and its phenanthroline adduct were studied by X‐ray diffraction. In Ph(Et)SnCl2 the tin atom is in a distorted tetrahedral environment, the distortion probably being imposed by weak intermolecular Sn· · ·Cl interactions. In [Ph(Et)SnCl2(phen)] the tin atom is in an octahedral trans‐C2, cis‐Cl2, N2 environment and weak intermolecular C–H· · ·Cl interactions connect the molecules throughout the lattice. Spectroscopic studies in solution (1H, 13C and 119Sn NMR) were also carried out; the 1H and 13C NMR data in dimethylsulfoxide suggest that [Ph(Et)SnCl2(phen)] remains at least partially undissociated in this solvent. Copyright © 2003 John Wiley & Sons, Ltd. |
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Keywords: | crystal structure 1H NMR 13C NMR 119Sn NMR mixed diorganotin complexes phenanthroline complexes |
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