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偶氮苯衍生物的自组装为有机凝胶和光响应液晶。

Self-Assembly of Azobenzene Derivatives into Organogels and Photoresponsive Liquid Crystals.

机构信息

Department of Chemistry, School of Sciences, and School of Materials Science and Engineering, Tianjin University, Tianjin, 300354, P. R. China.

出版信息

Chem Asian J. 2018 May 4;13(9):1173-1179. doi: 10.1002/asia.201800019. Epub 2018 Mar 30.

Abstract

A new class of coil-rod-coil molecules with an azobenzene core was synthesized. They were found to form robust organogels in several organic solvents. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), FTIR spectroscopy, UV/Vis absorption spectroscopy, H NMR spectroscopy, and X-ray diffraction (XRD) revealed that in these organogels, the molecules self-assembled into a nanofiber network with an H-type aggregation mode under the joint effect of π-π stacking, intermolecular hydrogen bonding, and van der Waals forces. Interestingly, the incorporation of the azobenzene mesogene into the rigid core led to photoisomerizable liquid crystal materials, which exhibited quick responsiveness to light and temperature, along with the trans-cis transition stimulated by UV light and heating.

摘要

一种新型的带有偶氮苯核心的线圈-棒-线圈分子被合成出来。研究发现,它们在几种有机溶剂中形成了坚固的有机凝胶。扫描电子显微镜(SEM)、透射电子显微镜(TEM)、原子力显微镜(AFM)、傅里叶变换红外光谱(FTIR)、紫外/可见吸收光谱、氢核磁共振光谱( H NMR)和 X 射线衍射(XRD)表明,在这些有机凝胶中,分子在π-π堆积、分子间氢键和范德华力的共同作用下自组装成具有 H 型聚集模式的纳米纤维网络。有趣的是,将偶氮苯介晶基元引入刚性核心中,得到了光致变色的液晶材料,它们对光和温度具有快速响应性,并且可以通过紫外光照射和加热来进行顺反异构转换。

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