Polar solvent-induced self-assembly of organic cocrystal helixes based on achiral molecules

IF 3.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Yuhao Ye , Lei Yao , Shulei Chen , Guan Wang , Yongyi Zhang , Tao Jin , Jing Zhang , Jing Che
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引用次数: 0

Abstract

Precise control over chirality in supramolecular structures has attracted significant attention in biology and optoelectronics. Herein, we report a novel helical cocrystal of organic donor−acceptor complex based on two achiral components. Depending on the solvent polarity, two red emissive cocrystals were self-assembled with different stacking manners. Notably, although the inversion symmetry of crystal lattice, strong solvent-solute interactions between polar crystal planes and acetonitrile governs the growth dynamics, to generate helical architectures. Furthermore, chiral additive tailoring was successfully established to regulate the supramolecular helix handedness which showed good circularly polarized luminescence performance, with an asymmetry factor (glum) of 0.005. This work demonstrates new pathway for chirality growth and tuning in circularly polarized optoelectronic devices and chiral recognition systems.

Abstract Image

极性溶剂诱导的基于非手性分子的有机共晶螺旋自组装
在超分子结构中对手性的精确控制已经引起了生物学和光电子学领域的广泛关注。在此,我们报道了一种基于两种非手性组分的有机供体-受体络合物的新型螺旋共晶。根据溶剂极性的不同,两个红色发射共晶以不同的堆叠方式自组装。值得注意的是,尽管晶格的反转对称,极性晶体平面与乙腈之间的强溶剂-溶质相互作用支配着生长动力学,从而产生螺旋结构。此外,成功地建立了手性添加剂裁剪来调节超分子螺旋旋向性,该超分子螺旋旋向性具有良好的圆偏振发光性能,其不对称系数(glum)为0.005。这项工作为圆偏振光电子器件和手性识别系统的手性生长和调谐提供了新的途径。
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来源期刊
Journal of Solid State Chemistry
Journal of Solid State Chemistry 化学-无机化学与核化学
CiteScore
6.00
自引率
9.10%
发文量
848
审稿时长
25 days
期刊介绍: Covering major developments in the field of solid state chemistry and related areas such as ceramics and amorphous materials, the Journal of Solid State Chemistry features studies of chemical, structural, thermodynamic, electronic, magnetic, and optical properties and processes in solids.
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