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Synthesis, crystal structures and spectroscopic properties of dichloroethylphenyltin(IV) and its phenanthroline adduct
Author(s) -
Casas José S.,
Castellano Eduardo E.,
Ellena Javier,
GarcíaTasende María S.,
Sánchez Agustín,
Sordo José,
Taboada Carmen,
Vidarte María J.
Publication year - 2003
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.552
Subject(s) - chemistry , adduct , crystal structure , crystallography , phenanthroline , octahedron , molecule , chloroform , intermolecular force , solvent , tin , nmr spectra database , x ray crystallography , stereochemistry , diffraction , spectral line , organic chemistry , physics , astronomy , optics
The reaction of dichloroethylphenyltin(IV), Ph(Et)SnCl 2 , with phenanthroline monohydrate (phen·H 2 O) in chloroform, in 1:1 mole ratio, afforded [Ph(Et)SnCl 2 (phen)]. The crystal structures of dichloroethylphenyltin(IV) and its phenanthroline adduct were studied by X‐ray diffraction. In Ph(Et)SnCl 2 the tin atom is in a distorted tetrahedral environment, the distortion probably being imposed by weak intermolecular Sn· · ·Cl interactions. In [Ph(Et)SnCl 2 (phen)] the tin atom is in an octahedral trans ‐C 2 , cis ‐Cl 2 , N 2 environment and weak intermolecular C–H· · ·Cl interactions connect the molecules throughout the lattice. Spectroscopic studies in solution ( 1 H, 13 C and 119 Sn NMR) were also carried out; the 1 H and 13 C NMR data in dimethylsulfoxide suggest that [Ph(Et)SnCl 2 (phen)] remains at least partially undissociated in this solvent. Copyright © 2003 John Wiley & Sons, Ltd.
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