Chemical Resources Laboratory, Tokyo Institute of Technology, R1-12 Nagatsuta, Midori-ku, Yokohama 226-8503, Japan.
Adv Mater. 2012 Nov 20;24(44):OP345-52. doi: 10.1002/adma.201204060. Epub 2012 Oct 18.
It is demonstrated that halogen bonding can be used to construct low-molecular-weight supramolecular complexes with unique light-responsive properties. In particular, halogen bonding drives the formation of a photoresponsive liquid-crystalline complex between a non-mesogenic halogen bond-donor molecule incorporating an azo group, and a non-mesogenic alkoxystilbazole moiety, acting as a halogen bond-acceptor. Upon irradiation with polarized light, the complex exhibits a high degree of photoinduced anisotropy (order parameter of molecular alignment > 0.5). Moreover, efficient photoinduced surface-relief-grating (SRG) formation occurs upon irradiation with a light interference pattern, with a surface-modulation depth 2.4 times the initial film thickness. This is the first report on a halogen-bonded photoresponsive low-molecular-weight complex, which furthermore combines a high degree of photoalignment and extremely efficient SRG formation in a unique way. This study highlights the potential of halogen bonding as a new tool for the rational design of high-performance photoresponsive suprastructures.
研究表明,卤键可用于构建具有独特光响应特性的低分子量超分子配合物。具体而言,卤键促使包含偶氮基团的非介晶卤键供体分子与非介晶烷氧基三唑部分之间形成光响应液晶配合物,后者充当卤键受体。经偏振光照射后,该配合物表现出高度的光致各向异性(分子取向有序参数>0.5)。此外,经光干涉图案照射后,可有效形成光致表面浮雕光栅(SRG),表面调制深度是初始膜厚的 2.4 倍。这是首例报道的卤键光响应低分子量配合物,它以独特的方式将高度的光取向和极其有效的 SRG 形成结合在一起。该研究强调了卤键作为合理设计高性能光响应超结构的新工具的潜力。