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热致显著晶体中的各向异性应变释放:分子重排的微观取向与宏观机械运动之间的相关性。

Anisotropic strain release in a thermosalient crystal: correlation between the microscopic orientation of molecular rearrangements and the macroscopic mechanical motion.

作者信息

Seki Tomohiro, Mashimo Takaki, Ito Hajime

机构信息

Division of Applied Chemistry , Frontier Chemistry Center , Faculty of Engineering , Hokkaido University , Sapporo , Hokkaido 060-8628 , Japan . Email:

Institute for Chemical Reaction Design and Discovery (WPI-ICReDD) , Hokkaido University , Sapporo , Hokkaido 060-8628 , Japan.

出版信息

Chem Sci. 2019 Mar 6;10(15):4185-4191. doi: 10.1039/c8sc05563g. eCollection 2019 Apr 21.

DOI:10.1039/c8sc05563g
PMID:31057747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6471989/
Abstract

The salient effect, which refers to a jumping phenomenon of organic and organometallic molecular crystals typically triggered by phase transitions in response to external stimuli, has been investigated intensively in the last five years. A challenging topic in this research area is the question of how to characterize the release of microscopic strain accumulated during phase transitions, which generates macroscopic mechanical motion. Herein, we describe the thermosalient effect of the triphenylethenyl gold 4-chlorophenyl isocyanide complex , which jumps reversibly at approximately -100 °C upon cooling at 50 °C min and heating at 30 °C min. Single-crystal X-ray diffraction measurements and differential scanning calorimetric analyses of suggest the occurrence of a thermal phase transition at this temperature. Detailed structural analyses indicate that anisotropic changes to the molecular arrangement occur in , whereby the crystallographic axis contracts upon cooling while the axis expands. Simultaneously, macroscopic changes of the crystal dimensions occur. This is observed as bending, , as an inclination of the crystal edges, and in the form of splitting, which occurs in a perpendicular direction to the major crystal axis. This study thus bridges the gap between macroscopic mechanical responses that are observed in high-speed photographic images and microscopic changes of the crystal structure, which are evaluated by X-ray diffraction measurements with face indexing.

摘要

显著效应是指有机和有机金属分子晶体的一种跳跃现象,通常由响应外部刺激的相变引发,在过去五年中已得到深入研究。该研究领域一个具有挑战性的课题是如何表征相变过程中积累的微观应变的释放,这种应变会产生宏观机械运动。在此,我们描述了三苯基乙烯基金4-氯苯基异氰化物配合物的热显著效应,该配合物在以50℃/分钟冷却和30℃/分钟加热时,在约-100℃时可逆地跳跃。单晶X射线衍射测量和差示扫描量热分析表明在此温度下发生了热相变。详细的结构分析表明,该配合物中分子排列发生了各向异性变化,即冷却时结晶学c轴收缩,而a轴膨胀。同时,晶体尺寸发生宏观变化。这表现为弯曲、晶体边缘倾斜以及在与主晶轴垂直方向上发生的分裂。因此,本研究填补了高速摄影图像中观察到的宏观机械响应与通过面索引X射线衍射测量评估的晶体结构微观变化之间的差距。

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