叔丁基二氯膦:晶体结构及其对超硅基钠的反应性

L. Fink, Marcel Bamberg, E. Alig, H. Lerner
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引用次数: 0

摘要

在80 °C/0.150 mbar下,通过短程升华获得了tBuPCl2晶体。基于x射线粉末数据确定了tBuPCl2的结构。测量是在173 K到rt的温度范围内进行的。在173 K时,x射线粉末模式被指定为正交相,而在213 K时,x射线粉末模式被指定为塑性结晶,立方相。我们进一步研究了tBuPCl2在室温下对Na(thf)2[SitBu3]的反应性。bupcl2与两种等效的Na(thf)2[SitBu3]反应,通过氯-钠交换,与tBu3SiCl一起生成未知的磷二化物Na2[PtBu]。Na2[PtBu]的身份被31P核磁共振光谱证实,它的存在被明确地证明了它与甲醇的质子化和随后形成的tBuPH2。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
tert-Butyldichlorophosphane: crystal structure and its reactivity towards supersilyl sodium
Abstract Crystals of tBuPCl2 were obtained by a short-path sublimation at 80 °C/0.150 mbar. The structure determination of tBuPCl2 was based on X-ray powder data. The measurements were carried out in a temperature range from 173 K to r. t. At 173 K the X-ray powder pattern has been assigned to an orthorhombic phase, and that at 213 K to a plastic-crystalline, cubic phase. We further investigated the reactivity of tBuPCl2 towards Na(thf)2[SitBu3] at ambient temperature. The reaction of tBuPCl2 with two equivalents of Na(thf)2[SitBu3] gave together with tBu3SiCl the yet unknown phosphanediide Na2[PtBu] by a chlorine-sodium exchange. The identity of Na2[PtBu] was confirmed by 31P NMR spectroscopy and its existence was unambiguously demonstrated by its protonation with methanol and the consequent formation of tBuPH2.
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