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在 : 一系列 中,分子的重定向动力学的热力学和动力学转变及相互作用方面 。

Thermodynamic and Dynamic Transitions and Interaction Aspects in Reorientation Dynamics of in : A Series of with .

机构信息

Polymer Institute of SAS, 845 41 Bratislava, Slovakia.

Department of Nuclear Chemistry, Faculty of Natural Sciences, Comenius University, 842 15 Bratislava, Slovakia.

出版信息

Int J Mol Sci. 2023 Sep 18;24(18):14252. doi: 10.3390/ijms241814252.

Abstract

The spectral and dynamic properties of in a series of ranging from to over a temperature range 100-300 K were investigated by ). The main characteristic ESR temperatures connected with slow to fast motion regime transition; 's and 's are situated above the corresponding glass temperatures, , and for the the 's lie above or close to melting point, , while the the < relationship indicates that the are in the local disordered regions of the . The 's and especially 's are compared with the dynamic crossover temperatures, = 8.72, as obtained by fitting the viscosity data in the liquid with the empirical power law. In particular, for > 6, the 's lie rather close to the resembling [PCCP 2018,,11145-11151], while for < 6, they are situated in the vicinity of . The absence of a coincidence for lower indicates that the is significantly influenced by the mutual interaction between the and the due to the increased polarity and proticity destroyed by the larger-scale melting transition.

摘要

在 100-300 K 的温度范围内,通过电子顺磁共振(ESR)研究了一系列 ()的光谱和动态性质。与慢到快的运动状态转变相关的主要特征 ESR 温度;'s 和 's 位于相应的玻璃化转变温度 、 之上,而对于 ,'s 位于或接近熔点 、 之上,而 〈 关系表明 处于 的局部无序区域。将 's 特别是 's 与通过拟合液体粘度数据得到的动态交叉温度 进行比较, = 8.72,该温度由经验幂律得出。特别是,对于 > 6,'s 非常接近 ,类似于 [PCCP 2018, 11145-11151],而对于 < 6,它们位于 附近。对于较低值没有一致的情况表明,由于极性和质子性的增加以及由较大规模的熔融转变破坏, 受到 和 之间相互作用的显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf2/10532429/e81b380f165b/ijms-24-14252-g001.jpg

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