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首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Electron Spin Resonance Study of Molecular Orientation and Dynamics of Phenyl Imino and Nitronyl Nitroxide Radicals in Organic 1D Nanochannels of Tris(o-phenylenedioxy)cyclotriphosphazene
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Electron Spin Resonance Study of Molecular Orientation and Dynamics of Phenyl Imino and Nitronyl Nitroxide Radicals in Organic 1D Nanochannels of Tris(o-phenylenedioxy)cyclotriphosphazene

机译:苯基亚氨基和硝基硝基氧化物基团中的分子取向和动力学研究Tris(O-苯二烷基二氧基)环氨基膦嘧啶的分子取向和动力学研究

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摘要

Imino and nitronyl nitroxide (IN and NN, respectively) radicals such as phenyliminonitroxide (PhIN) and phenylnitronylnitroxide (PhNN), respectively, were dispersed in the organic 1D nanochannels of tris(o-phenylenedioxy)-cyclotriphosphazene (TPP). Electron spin resonance (ESR) measurements were conducted on these inclusion compounds (ICs) in the temperature range 4.2-300 K. The modulated-septet ESR spectra of TPP ICs using PhIN observed in the range 165-258 K were reproduced with the EasySpin program package using a model in which some of the PhIN molecules underwent uniaxial rotational diffusion in the TPP nanochannels around the molecular long axis corresponding to the principal y-axis of the g tensor. However, for the TPP IC using PhNN, complicated ESR spectra were observed, which were not consistent with the modulated quintet observed in solution or in the fast-motion limit in solids. These spectra were reproduced by the superposition of a quintet originating from rotational diffusion of PhNN molecules and a septet based on rotational diffusion of PhIN molecules generated in the synthetic process. The rotational diffusion activation energies of PhIN and PhNN in the TPP nanochannels were estimated to be 19 and 45 kJ mol(-1) using an Arrhenius plot, respectively. These were consistent with that for NN radicals in the 1D nanochannels of 2,4,6-tris(4-chlorophenoxy)-1,3,5-triazine (CLPOT) (37-54 kJ mor l ) with a larger pore diameter than TPP reported in our previous study, or with that for 4-substituted-2,2,6,6-tetramethyl-l-piperidinyloxyl (4-X-TEMPO) in TPP nanochannels (5-26 kJ mol(-1)) with regard to molecular size or host-guest or guest-guest interactions. These results indicate that not only the NN group but also IN may be used for the clarification of chemical or biological structures of nanomaterials such as nanosized cavities.
机译:亚氨基和氮氧自由基(分别IN和NN,)基团如phenyliminonitroxide(PHIN)和phenylnitronylnitroxide(PhNN),分别分散在三有机1D纳米通道(邻亚苯基二氧基)-cyclotriphosphazene(TPP)。电子自旋共振(ESR)测量在温度范围4.2-300 K的这些包合物(ICS)进行调制,七重峰ESR使用PHIN TPP IC的光谱在165-258 k中的范围内观察到被与EasySpin程序再现打包使用模型,其中一些PHIN分子在围绕对应于克张量的主y轴上的分子长轴的TPP纳米通道进行单轴旋转扩散。然而,对于使用PhNN TPP的IC,复杂ESR谱中观察到,这是不与溶液中或在固体快速运动极限中观察到的经调制的五重峰一致。这些光谱通过从PhNN分子的旋转扩散和基于在所述合成过程中产生的PHIN分子的旋转扩散一个七重峰一个五重峰始发的叠加再现。在TPP纳米通道PHIN和PhNN的旋转扩散活化能估计为使用阿累尼乌斯曲线图19和45千焦耳摩尔(-1),分别。这些是与用于与更大的孔径比1D纳米通道2,4,6-三(4-氯苯氧基)-1,3,5-三嗪(CLPOT)(37-54千焦MOR升)的NN基团一致的TPP报道我们以前的研究,或与4-取代基-2,2,6,6-四甲基-1-哌啶基氧基在TPP纳米通道(4-X-TEMPO)(5-26千焦摩尔(-1))以把分子大小或其主客体或客体 - 客体相互作用。这些结果表明,不仅NN组,而且在可用于澄清如纳米空腔纳米材料的化学或生物结构。

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