首页> 外文会议>Fraunhofer-Institut fur Chemische Technologie(ICT) International Annual Conference; 20060627-30; Karlsruhe(DE) >Preparation and Solid State ~(13)C-NMR of the Four Stable Phases of 2,4,6,8,10,12-Hexanitro-2,4,6,8,10,12-hexaazatetracyclo5.5.0.0~(5.9).0~(3,11)dodecane (HNIW, CL 20)
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Preparation and Solid State ~(13)C-NMR of the Four Stable Phases of 2,4,6,8,10,12-Hexanitro-2,4,6,8,10,12-hexaazatetracyclo5.5.0.0~(5.9).0~(3,11)dodecane (HNIW, CL 20)

机译:2,4,6,8,10,12-六硝基-2,4,6,8,10,12-六氮杂四环5.5.0.0〜()的四个稳定相的制备及固态〜(13)C-NMR 5.9).0〜(3,11)十二烷(HNIW,CL 20)

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摘要

CL 20 was prepared in a four step synthesis by a variation of Nielsen's classical method. This produced the alpha hydrated phase of CL 20. The other polymorphs were prepared by solution/precipitation in selected solventon-solvent pairs. The phase transitions obtained were alpha to beta, beta to gamma and beta to epsilon. FT-IR spectra of some polymorphs were recorded. Solid state ~(13)C NMR was done under cross polarisation conditions with magic angle spinning and a tentative assignment of the signals was attempted.
机译:CL 20是通过改变尼尔森经典方法的四步合成法制备的。这产生了CL 20的α水合相。通过在选定的溶剂/非溶剂对中进行溶液/沉淀来制备其他多晶型物。获得的相变是α到β,β到γ和β到ε。记录了一些多晶型物的FT-IR光谱。固态〜(13)C NMR是在交叉极化条件下用魔角旋转完成的,并尝试对信号进行初步分配。

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