Li Yu-Hao, Cui Min, Gong Yi, Xu Tian-Yi, Tong Fei
Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
Materials (Basel). 2024 Jul 24;17(15):3664. doi: 10.3390/ma17153664.
Harnessing the photoinduced phase transitions in organic crystals, especially the changes in shape and structure across various dimensions, offers a fascinating avenue for exact spatiotemporal control, which is crucial for developing future smart devices. In our study, we report a new photoactive molecular crystal made from ()-2-(3-phenyl-allylidene)malonate (()-PADM). When exposed to ultraviolet (UV) light at 365 nm, this compound experiences an -to- photoisomerization in liquid solution and a crystal-to-liquid phase transition in solid crystals. Remarkably, nanoscopic crystalline rods boost their melting rate and degree compared to bulk crystals, indicating that miniaturization enhances the photoinduced melting effect. Our results demonstrate a simple approach to rapidly drive molecular crystals into liquids via photochemical reactions and phase transitions.
利用有机晶体中的光致相变,特别是跨不同维度的形状和结构变化,为精确的时空控制提供了一条引人入胜的途径,这对于开发未来的智能设备至关重要。在我们的研究中,我们报道了一种由()-2-(3-苯基-亚烯丙基)丙二酸酯(()-PADM)制成的新型光活性分子晶体。当暴露于365nm的紫外光时,该化合物在液体溶液中经历 - 到 - 的光异构化,并在固体晶体中发生晶体到液体的相变。值得注意的是,与块状晶体相比,纳米级晶棒提高了它们的熔化速率和程度,表明小型化增强了光致熔化效应。我们的结果展示了一种通过光化学反应和相变将分子晶体快速驱动到液体中的简单方法。