Harmgarth Nicole, Liebing Phil, Hillebrand Philipp, Busse Sabine, Edelmann Frank T
Chemisches Institut der Otto-von-Guericke-Universität Magdeburg, Universitätsplatz 2, 39106 Magdeburg, Germany.
ETH Zurich, Laboratory for Inorganic Chemistry, Vladimir-Prelog-Weg 1-5/10, 8093, Zurich, Switzerland.
Acta Crystallogr E Crystallogr Commun. 2017 Sep 12;73(Pt 10):1443-1448. doi: 10.1107/S2056989017012671. eCollection 2017 Oct 1.
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.
2当量的锂碳硼烷脒基锂Li[-(CHB)C(NCy)(NHCy)]与SnCl在四氢呋喃中反应,得到亚锡烯化合物双(,'-二环己基脒基碳硼烷酸根)锡(II),Sn[-(CHB)C(NCy)(NHCy)] ()。SnCl与2当量的Li[-(CHB)C(N Pr)(NH Pr)]的类似反应意外地得到了已知的溶剂化五氯锡酸(IV)盐[Li(THF)][SnCl(THF)]作为主要反应产物。少量新的氯锡(IV)双(碳硼烷脒基)双(,'-二异丙基脒基碳硼烷酸根)氯化锡(IV),SnCl[-(CHB)C(N Pr)(NH Pr)][-(CHB)C(N Pr)] ()作为副产物被分离出来。单晶X射线结构分析表明,在 和 中碳硼烷脒基配体均为 ,-螯合配位。 中的Sn原子在一个立体活性孤对的参与下采取伪三角双锥配位。在 中,Sn的三角双锥配位由一个氯配体完成。