偶氮苯
弯曲
构象异构
外消旋混合物
材料科学
辐照
弯曲分子几何
结晶学
光化学
光学
分子物理学
异构化
对映体
化学
复合材料
立体化学
聚合物
有机化学
物理
分子
催化作用
核物理学
作者
Takuya Taniguchi,Juri Fujisawa,Motoo Shiro,Hideko Koshima,Toru Asahi
标识
DOI:10.1002/chem.201505149
摘要
Abstract The photomechanical motion of chiral crystals of trans ‐azobenzene derivatives with an ( S )‐ and ( R )‐phenylethylamide group was investigated and compared with a racemic crystal. Changes in the UV/Vis absorption spectra of the powdered crystals before and after UV irradiation were measured by using an optical waveguide spectrometer, showing that the lifetime of the cis ‐to‐ trans thermal back‐isomerization of the chiral crystals was faster than that of the racemic crystals. Upon UV irradiation, a long plate‐like chiral microcrystal bent away from the light source with a twisting motion. A square‐like chiral microcrystal curled toward the light with some twisting. Reversible bending of a rod‐like chiral microcrystal was repeatable over twenty‐five cycles. In contrast, bending of a plate‐like racemic microcrystal was small. A possible mechanism for the bending and twisting motion was discussed based on the optimized cis conformer determined by using calculations, showing that the bending motion with twisting is caused by elongation along the b axis and shrinkage along the a axis.
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