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Covalent Inorganic Azides

机译:共价无机叠氮化物

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The chemistry of covalent inorganic azides originated with the synthesis of aqueous HN_3 solutions by Tony Curtis in 1890. A link later, in. 1900. it proved possible to prepare iodine azide, IN_3, as the first member of the meanwhile com-piete seriesof halogen azides. Since .then it has been possible to synthesize, in addition to HN_3 and the stable salt H_2N_3~+SbF_6~-, azide compounds of elements from Groups 13 to 17. In these compounds the N_3 moiety acts as a pseudohalogen and is primarily cova-lently coordinated to the nonmetal. On-ly a few organic azides, however, as well as HN_3. H_2N_3~+, and all halogen azides have been thoroughly studied with respect to structure and bonding. The combined application of diffraction methods (X-ray and electron diffraction) and microwave spectroscopy together with quantum chemical approaches such as ab initio SCF and density functional calculations have led in the last few years to an improved understanding of the molecular properties of numerous nonmetalazides, almost all of which are explosive. This interaction of theory and experiment has greatly enhanced the development of azide chemistry and has led to realistic expectations for the synthesis of as yet unknown non-metal azides.
机译:共价无机叠氮化物的化学起源于1890年托尼·柯蒂斯(Tony Curtis)合成HN_3水溶液。后来的一个链接是1900年。证明有可能制备碘叠氮化物IN_3,作为同时卤化物的系列化合物的第一个成员。叠氮化物。从那时起,除了HN_3和稳定的盐H_2N_3〜+ SbF_6〜-之外,还可以合成第13-17组元素的叠氮化物。在这些化合物中,N_3部分用作拟卤素,主要是甲壳素。与非金属紧密协调。但是,仅一些有机叠氮化物以及HN_3。 H_2N_3〜+以及所有卤素叠氮化物均已在结构和键合方面进行了深入研究。过去几年中,衍射方法(X射线和电子衍射)和微波光谱技术以及量子化学方法(从头算SCF)和密度泛函计算的结合应用,导致人们对许多非金属叠氮化物的分子特性有了更好的了解,几乎所有这些都是爆炸性的。理论与实验的这种相互作用极大地促进了叠氮化物化学的发展,并导致人们对合成未知金属非叠氮化物的现实期望。

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