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首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >Synthesis of spirocyclic aminosilanes with electron withdrawing substituents at nitrogen
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Synthesis of spirocyclic aminosilanes with electron withdrawing substituents at nitrogen

机译:用电子取代基在氮气中合成螺环氨硅烷

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摘要

The first synthesis of spirocyclic tetrasulfonamidosilanes is described. According to the X-Ray structure analysis of the most stable tetratosylamidosilane obtained the Silicon is bonded to four Nitrogen atoms in a spirocycle and surrounded by four Oxygen atoms which are located above the planes of the SiN4 tetrahedron. [References: 29]
机译:描述了螺环氧丙胺硅氧烷的第一次合成。 根据所得最稳定的四氰基氨基硅烷的X射线结构分析,硅在螺旋形循环中键合到四个氮原子中,并被四个氧原子包围,该氧原子位于SIN4四面体的平面上方。 [参考:29]

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