Hofmann型和Hofmann-(en)型吡咯包合物结构和动力学的X射线和2H NMR研究

Shin-ichi Nishikiori , Akiji Takahashi , Christopher I Ratcliffe , John A Ripmeester
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引用次数: 12

摘要

用单晶X射线晶体学、固态2H NMR、PXRD、TGA和DSC研究了Hofmann和Hoffmann en型吡咯包合物Cd(NH3)2Ni(CN)4.2C4H4NH和Cd(en)Ni(CN)4.2 C4H4NH。两者都显示出吡咯在不等价的六位势中的平面内重新定向,具有两个低能量极小值,其中吡咯的N相对于晶体c轴向上或向下定向,随后是关于平行于晶体c轴的轴的平面外4倍运动。还有证据表明,存在2倍而不是4倍运动的中间动态状态。主体框架的NH3或en基团围绕晶体c方向旋转。Hofmann-en-吡咯包合物在196和259K处显示出两个相变,并且主体-en和吡咯-客体的动力学似乎与后一个结构转变密切相关。将这些吡咯包合物的结果与先前获得的两种等效苯包合物进行了比较,并用300 K以上Cd(en)Ni(CN)4·2C6D6的新的2H NMR线形数据进行了补充。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
X-ray and 2H NMR studies of structure and dynamics in the Hofmann-type and the Hofmann-(en)-type pyrrole clathrates

Structure and dynamics in the Hofmann and Hoffmann-en type pyrrole clathrates, Cd(NH3)2Ni(CN)4·2C4H4NH and Cd(en)Ni(CN)4·2C4H4NH, have been studied by single crystal X-ray crystallography, solid state 2H NMR, PXRD, TGA and DSC. Both show in-plane reorientation of the pyrrole in an inequivalent six-site potential, with two low energy minima where the N of the pyrrole is oriented up or down with respect to the crystal c axis, followed by out-of-plane 4-fold motion about an axis parallel to the crystal c axis. There is also evidence for an intermediate dynamic state where there is 2-fold rather than 4-fold motion. The NH3 or en groups of the host frameworks rotate about the crystal c direction. The Hofmann-en pyrrole clathrate shows two phase transitions at 196 and 259 K, and the dynamics of the host en and pyrrole guest appear to be intimately linked to the latter structural transition. The results for these pyrrole clathrates have been compared with those for the two equivalent benzene clathrates, obtained previously and augmented with new 2H NMR lineshape data for Cd(en)Ni(CN)4·2C6D6 above 300 K.

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