Synthesis and crystal structures of two new tin bis-(carboranylamidinate) complexes.

Acta Crystallogr E Crystallogr Commun

Chemisches Institut der Otto-von-Guericke-Universität Magdeburg, Universitätsplatz 2, 39106 Magdeburg, Germany.

Published: October 2017

Reaction of 2 equiv. of the lithium carboranylamidinate Li[-(CHB)C(NCy)(NHCy)] with SnCl in THF afforded the stannylene compound bis(,'-dicyclohexylamidinatocarboranate)tin(II), Sn[-(CHB)C(NCy)(NHCy)] (). A similar reaction of SnCl with 2 equiv. of Li[-(CHB)C(N Pr)(NH Pr)] unexpectedly afforded the known solvated penta-chlorido-stannate(IV) salt [Li(THF)][SnCl(THF)] as the main reaction product. Small amounts of the new chlorido-tin(IV) bis-(carboranylamidinate) bis(,'-diiso-propylamidinatocarboranate)chloridotin(IV), SnCl[-(CHB)C(N Pr)(NH Pr)][-(CHB)C(N Pr)] (), were isolated as a by-product. Single-crystal X-ray structure analysis revealed a ,-chelating coordination of the carboranylamidinate ligands in both and . The Sn atom in adopts a pseudo-trigonal-bipyramidal coordination under participation of a stereoactive lone pair. In , a trigonal-bipyramidal coordination of Sn is completed by a chlorido ligand.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730292PMC
http://dx.doi.org/10.1107/S2056989017012671DOI Listing

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