Institute of Chemistry, 18059 Rostock, Albert-Einstein-Str. 3a, Germany.
Dalton Trans. 2018 Dec 18;48(1):125-132. doi: 10.1039/c8dt04295k.
Various tin(ii) compounds such as Mes2Sn (Mes = 2,4,6-tri-tert-butylphenyl), Sn[N(SiMe3)2]2 and TerSnCl (Ter = 2,6-bis(2,4,6-trimethylphenyl)phenyl) could be readily oxidised by organic azides to release N2, forming nitrogen-tin compounds. Depending on the used Sn(ii) compound, the reactions with two equivalents of azide led to the formation of tetrazastannoles (R2N4SnR'2) or cyclo-distannadiazanes [R2Sn(μ-NR')]2. The reactivity was independent of the electronic situation of the organic azide. Additionally, Mes*2Sn formed an amido-azido compound of the type R(R')Sn(N(SiMe3)2)N3 in the presence of Me3SiN3. Presumably, the corresponding tetrazastannole was formed in the first step followed by a ring opening reaction. The same holds true for the reaction of Sn[N(SiMe3)2]2 with Me3SiN3 while TerSnCl showed no reaction in the presence of Me3SiN3, even after prolonged heating.
各种锡(II)化合物,如 Mes2Sn(Mes=2,4,6-三-叔丁基苯基)、Sn[N(SiMe3)2]2 和 TerSnCl(Ter=2,6-双(2,4,6-三甲基苯基)苯基),可被有机叠氮化物轻易氧化,释放出氮气,形成氮锡化合物。根据所使用的 Sn(II)化合物的不同,与两当量的叠氮化物反应会导致四唑基锡(R2N4SnR'2)或环二锡氮烷[R2Sn(μ-NR')]2 的形成。反应与有机叠氮化物的电子情况无关。此外,Mes*2Sn 在 Me3SiN3 的存在下形成了类型为 R(R')Sn(N(SiMe3)2)N3 的酰胺-叠氮化合物。据推测,首先形成相应的四唑基锡,然后发生开环反应。Sn[N(SiMe3)2]2 与 Me3SiN3 的反应也是如此,而 TerSnCl 在 Me3SiN3 的存在下没有反应,即使在长时间加热后也是如此。