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Hyperpolarized ~(129)Xe NMR spectroscopic investigation of potentially porous shape-persistent macrocyclic materials

机译:超极化〜(129)Xe NMR光谱研究潜在的多孔形状持久大环材料

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摘要

The application of continuous-flow hyperpolarized ~(129)Xe NMR spectroscopy to investigate the pores of three shape-persistent organic macrocycles is described.Peaks with xenon chemical shifts between 160 and 200 ppm are assigned to xenon atoms trapped in highly confined pores while NMR peaks with chemical shifts of 100 to 140 ppm are assigned to xenon present in channels that exist through the centre of the stacked macrocycles.With the aid of molecular dynamics simulations,connections between the ~(129)Xe NMR spectra and the X-ray diffraction structure of one of the solvated macrocycles,1,have been made.The similarities in the ~(129)Xe NMR spectra of the three compounds containing hyperpolarized xenon suggest that all three hosts possess comparable pore structures.The ~(129)Xe NMR data provide information about the porous nature of the two compounds for which X-ray crystallographic analysis was not possible.Data obtained from two-dimensional ~(129)Xe NMR exchange spectroscopy experiments,variable-temperature ~(129)Xe NMR and molecular dynamics simulations suggest a mechanism whereby the xenon gains access to the highly confined sites via the channels.
机译:描述了应用连续流超极化〜(129)Xe NMR光谱研究三个形状持久的有机大环的孔,将氙化学位移介于160和200 ppm之间的峰分配给捕获在高度受限孔中的氙原子化学位移为100至140 ppm的峰被分配给存在于通过堆积大环中心存在的通道中的氙。借助分子动力学模拟,〜(129)Xe NMR光谱与X射线衍射之间的联系已制得其中一个溶剂化大环化合物1的结构。三种含超极化氙的化合物的〜(129)Xe NMR光谱相似,表明这三个主体均具有可比的孔结构。〜(129)Xe NMR数据提供了无法进行X射线晶体学分析的两种化合物的多孔性质的信息。从二维〜(129)Xe NMR交换光谱实验获得的数据nts,〜(129)Xe变温NMR和分子动力学模拟提出了一种机制,通过该机制,氙气可以通过通道进入高度受限的位置。

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