Kajitani Takashi, Motokawa Kyuri, Kosaka Atsuko, Shoji Yoshiaki, Haruki Rie, Hashizume Daisuke, Hikima Takaaki, Takata Masaki, Yazawa Koji, Morishima Ken, Shibayama Mitsuhiro, Fukushima Takanori
Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.
RIKEN SPring-8 Center, Sayo, Hyogo, Japan.
Nat Mater. 2019 Mar;18(3):266-272. doi: 10.1038/s41563-018-0270-7. Epub 2019 Jan 21.
The self-assembly of organic molecules into supramolecular materials with structural ordering beyond the nanometre scale is challenging. Here, we report the spontaneous self-assembly of a chiral discotic triphenylene derivative into millimetre-sized droplets. The structure of the droplets is characterized by high positional and orientational ordering and a three-dimensional integrity similar to that of single crystals. Notwithstanding, these assemblies slide when placed on a vertical substrate demonstrating their fluid nature. X-ray imaging shows that during the sliding process the internal crystal-like structure is maintained and that the droplets undergo clockwise or counterclockwise unidirectional rotation, depending on the chirality of their molecular components. Rheological measurements suggest that this rotational behaviour might result from the distinct yield stress between the (R)- and (S)-enantiomers. Overall, our findings demonstrate that molecular chirality can determine the movement direction of a supramolecular structure, thus expanding the fundamental understanding of the structure and dynamics of soft materials.
将有机分子自组装成具有超越纳米尺度结构有序性的超分子材料具有挑战性。在此,我们报道了一种手性盘状三亚苯衍生物自发自组装成毫米级液滴。这些液滴的结构具有高度的位置和取向有序性以及类似于单晶的三维完整性。尽管如此,这些组装体放置在垂直基板上时会滑动,表明它们具有流体性质。X射线成像显示,在滑动过程中,内部类似晶体的结构得以维持,并且液滴会根据其分子组分的手性进行顺时针或逆时针单向旋转。流变学测量表明,这种旋转行为可能源于(R)-和(S)-对映体之间不同的屈服应力。总体而言,我们的研究结果表明,分子手性可以决定超分子结构的运动方向,从而扩展了对软材料结构和动力学的基本认识。