Institut für Anorganische Chemie der Universität Göttingen, Germany.
Inorg Chem. 2010 Apr 5;49(7):3461-4. doi: 10.1021/ic100031d.
The reaction of beta-diketiminate substituted tin(II) chloride, LSnCl (1; L = HC{(CMe)(2,6-iPr(2)C(6)H(3)N)}(2)), with the lithium salt of trimethylsilyl diazomethane (LiC(N(2))SiMe(3)) is described. In the course of the reaction, the exclusive formation of tin(II) substituted carbodiimide LSnNCNSiMe(3) (2) is observed in good yield. This reaction occurs at room temperature without any side products. Furthermore, we reacted diiron nonacarbonyl, Fe(2)(CO)(9), with compound 2 to confirm the carbodiimide skeleton (N=C=N) without rearrangement. The latter reaction leads to the tin(II) coordinate iron carbonyl complex LSnNCNSiMe(3)Fe(CO)(4) (3). Compounds 2 and 3 were investigated by microanalysis and multinuclear NMR spectroscopy and were further characterized by X-ray structural analysis.
β-二酮亚胺取代的二氯化锡(LSnCl,1;L = HC{(CMe)(2,6-iPr(2)C(6)H(3)N)}(2))与三甲基硅基重氮甲烷的锂盐(LiC(N(2))SiMe(3)反应。在反应过程中,以良好的收率观察到锡(II)取代的碳二亚胺 LSnNCNSiMe(3)(2)的唯一形成。该反应在室温下进行,没有任何副产物。此外,我们还使二铁九羰基反应,Fe(2)(CO)(9)与化合物 2 反应,以确认没有重排的碳二亚胺骨架(N=C=N)。后一反应导致锡(II)配位的铁羰基配合物 LSnNCNSiMe(3)Fe(CO)(4)(3)。通过微量分析和多核 NMR 光谱研究了化合物 2 和 3,并通过 X 射线结构分析进一步进行了表征。