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五配位磷在氮化磷酰亚胺 P4N6(NH) 的高压多晶型物中。

Pentacoordinate phosphorus in a high-pressure polymorph of phosphorus nitride imide P4N6(NH).

机构信息

Department Chemie, Lehrstuhl für Anorganische Festkörperchemie, Ludwig-Maximilians-Universität München, Butenandtstrasse 5-13, 81377 München (Germany) http://www.cup.uni-muenchen.de/ac/schnick.

出版信息

Angew Chem Int Ed Engl. 2014 Dec 22;53(52):14490-3. doi: 10.1002/anie.201406086. Epub 2014 Aug 14.

Abstract

Coordination numbers higher than usual are often associated with superior mechanical properties. In this contribution we report on the synthesis of the high-pressure polymorph of highly condensed phosphorus nitride imide P4 N6 (NH) representing a new framework topology. This is the first example of phosphorus in trigonal-bipyramidal coordination being observed in an inorganic network structure. We were able to obtain single crystals and bulk samples of the compound employing the multi-anvil technique. γ-P4 N6 (NH) has been thoroughly characterized using X-ray diffraction, solid-state NMR and FTIR spectroscopy. The synthesis of γ-P4 N6 (NH) gives new insights into the coordination chemistry of phosphorus at high pressures. The synthesis of further high-pressure phases with higher coordination numbers exhibiting intriguing physical properties seems within reach.

摘要

通常,配位数高于常规的物质往往具有更优异的机械性能。在本研究中,我们报道了高度缩合磷氮酰亚胺 P4N6(NH)的高压多晶型物的合成,其代表了一种新的骨架拓扑结构。这是首次在无机网络结构中观察到磷呈三角双锥配位。我们采用多砧技术获得了该化合物的单晶和块状样品。利用 X 射线衍射、固态 NMR 和傅里叶变换红外光谱对 γ-P4N6(NH)进行了全面的表征。γ-P4N6(NH)的合成使我们对高压下磷的配位化学有了新的认识。进一步合成具有更高配位数、表现出有趣物理性质的高压相似乎也触手可及。

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