4 resultados para Hypercoordination


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The reaction of Me3SbCl2 and (Me2SnS)3 afforded the complex (Me3SbS)2Me2SnCl2 in high yields, whose molecular structure features both hypercoordinated tin and antimony atoms. In solution, (Me3SbS)2Me2SnCl2 undergoes a reversible dissociation and ligand interchange reaction to give Me3SbS, Me3SbCl2 and (Me2SnS)3.

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A strategy for the preparation of the otherwise difficult to obtain binary organometallic oxides containing two heavy main group elements is described and exemplified by the synthesis of [(p-MeOC6H4)2Te(OSnt-Bu2OH)2]2.

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The reaction of diorganotin sulfides, cyclo-(R2SnS)n (R=Me, n-Bu; n=3; R=t-Bu; n=2) with the corresponding diorganotin dichlorides, R2SnCl2, provided the tetraorganodistannathianes, (R2ClSn)2S (1, R=Me; 2, R=n-Bu; 3, R=t-Bu). 1H-, 13C-, and 119Sn-NMR studies indicate that these compounds are kinetically labile and in equilibrium with the starting materials. Addition of equimolar amounts of [(Ph3P)2N]Cl to the reaction mixtures gave the chloride complexes [(Ph3P)2N]+[S(SnR2Cl)2Cl] (4, R=Me; 5, R=n-Bu; 6, R=t-Bu). Single-crystal X-ray diffraction studies revealed the tin atoms in both 4 and 6 to adopt distorted trigonal bipyramidal configurations with the chlorine atoms occupying the axial positions.


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The crystal and molecular structure of Gingras' salt [n-Bu4N]+ [Ph3SnF2] is reported, which reveals a variety of inter- and intramolecular C---H...F hydrogen bonding interactions. A 119Sn MAS-NMR spectrum was recorded and a tensor analysis has been performed according to the method of Herzfeld and Berger. The results are discussed in terms of the molecular structure and are compared with the parent compound Ph3SnF as well as with Mes3SnF (Mes=mesityl).