Campbell Rory, Davis Martin F, Fazakerley Mathew, Portius Peter
Department of Chemistry, The University of Sheffield, Brook Hill, S3 7HF (UK) https://www.sheffield.ac.uk/chemistry/staff/profiles/peter_portius.
Chemistry. 2015 Dec 14;21(51):18690-8. doi: 10.1002/chem.201503478. Epub 2015 Nov 13.
The first charge-neutral Lewis base adducts of tin(IV) tetraazide, [Sn(N3)4(bpy)], [Sn(N3)4(phen)] and [Sn(N3)4(py)2], and the salt bis{bis(triphenylphosphine)iminium} hexa(azido)stannate [(PPN)2Sn(N3)6] (bpy = 2,2'-bipyridine; phen = 1,10-phenanthroline; py = pyridine; PPN = N(PPh3)2) have been prepared using covalent or ionic azide-transfer reagents and ligand-exchange reactions. The azides were isolated on the 0.3 to 1 g scale and characterized by IR and NMR spectroscopies, microanalytical and thermal methods and their molecular structures determined by single-crystal XRD. All complexes have a distorted octahedral Sn[N]6 coordination geometry and possess greater thermal stability than their Si and Ge homologues. The nitrogen content of the adducts of up to 44% exceed any Sn(IV) compound known hitherto.
四叠氮锡(IV)的首个电荷中性路易斯碱加合物[Sn(N₃)₄(bpy)]、[Sn(N₃)₄(phen)]和[Sn(N₃)₄(py)₂],以及盐双{双(三苯基膦)亚胺鎓}六(叠氮基)锡酸盐[(PPN)₂Sn(N₃)₆](bpy = 2,2'-联吡啶;phen = 1,10-菲咯啉;py = 吡啶;PPN = N(PPh₃)₂)已通过共价或离子型叠氮基转移试剂及配体交换反应制备而成。这些叠氮化合物以0.3至1克的规模分离得到,并通过红外光谱和核磁共振光谱、微量分析和热分析方法进行表征,其分子结构通过单晶X射线衍射确定。所有配合物都具有扭曲的八面体Sn[N]₆配位几何结构,并且比它们的硅和锗同系物具有更高的热稳定性。加合物中高达44%的氮含量超过了迄今为止已知的任何四价锡化合物。