Department of Chemical Engineering, National Tsing Hua University, No. 101, Section 2, Kuang-Fu Road, Hsinchu, Taiwan 30013, ROC.
Chemistry. 2012 Jul 16;18(29):9091-8. doi: 10.1002/chem.201200057. Epub 2012 Jun 11.
Herein, two asymmetric chiral bent-core molecules, 3-[(4-{[4-(heptyloxy)benzoyl]oxy}benzoyl)oxy]-phenyl-4-[(4-{[(1R)-1-methylheptyl]oxy}benzoyl)oxy] benzoate (BC7R) and 3-[(4-{[4-(heptyloxy)benzoyl]oxy}benzoyl)oxy]-phenyl-4-[(4-{[(1S)-1-methylheptyl]oxy}benzoyl)oxy] benzoate (BC7S), were synthesized to demonstrate control of the helicity of their self-assembled hierarchical superstructures. Mirror-imaged CD spectra showed a split-type Cotton effect after the formation of self-assembled aggregates of BC7R and BC7S, thereby suggesting the formation of intermolecular exciton couplets with opposite optical activities. Both twisted and helical ribbons with preferential helicity that corresponded to the twisting character of the intermolecular exciton couplet were found in the aggregates. The formation of helical ribbons was attributed to the merging of twisted ribbons through an increase in width to improve morphological stability. As a result, control of the helicity of hierarchical superstructures from the self-assembly of bent-core molecules could be achieved by taking advantage of the transfer of chiral information from the molecular level onto the hierarchical scale.
本文合成了两种不对称手性双锥分子,3-[(4-({[4-(庚氧基)苯甲酰基]氧基}苯甲酰基)氧基]苯基-4-[(4-({[(1R)-1-甲基庚基]氧基}苯甲酰基)氧基]苯甲酰基)苯甲酸酯(BC7R)和 3-[(4-({[4-(庚氧基)苯甲酰基]氧基}苯甲酰基)氧基]苯基-4-[(4-({[(1S)-1-甲基庚基]氧基}苯甲酰基)氧基]苯甲酰基)苯甲酸酯(BC7S),以证明其自组装分级超结构的手性控制。BC7R 和 BC7S 自组装聚集体形成后,圆二色谱显示出分裂型 Cotton 效应,从而表明形成了具有相反光学活性的分子间激子偶极子。在聚集体中发现了具有优先手性的扭曲和螺旋带,与分子间激子偶极子的扭曲特征相对应。螺旋带的形成归因于通过增加宽度来合并扭曲带,以提高形态稳定性。因此,通过利用手性信息从分子水平传递到分级尺度,可以实现从双锥分子自组装到分级超结构的手性控制。