Jiao Shaoshao, Shen Pingchuan, Li Jinshi, Dong Xiaobin, Tang Ben Zhong, Zhao Zujin
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology, Guangzhou, 510640, China.
School of Science and Engineering, Shenzhen Institute of Aggregate Science and Technology, The Chinese University of Hong Kong, Shenzhen, Guangdong, 518172, China.
Angew Chem Int Ed Engl. 2025 Jan 10;64(2):e202414801. doi: 10.1002/anie.202414801. Epub 2024 Oct 25.
Developing long-chain molecules with stable helical structures is of significant importance for understanding and modulating the properties and functions of helical biological macromolecules, but challenging. In this work, an effective and facile approach to stabilize folded helical structures by strengthening through-space conjugation is proposed, using new ortho-hexaphenylene (o-HP) derivatives as models. The structure-activity relationship between the through-space conjugation and charge-transport behavior of the prepared folded helical o-HP derivatives is experimentally and theoretically investigated. It is demonstrated that the through-space conjugation within o-HP derivatives can be strengthened by introducing electron-withdrawing pyridine and pyrazine rings, which can effectively stabilize the helical structures of o-HP derivatives. Moreover, scanning tunneling microscopy-break junction measurements reveal that the stable regular helical structures of o-HP derivatives open-up dominant through-space charge-transport pathways, and the single-molecule conductance is enhanced by more than 70 % by strengthening through-space conjugation with pyridine and pyrazine. However, the through-bond charge transport pathways contribute much less to the conductance of o-HP derivatives. These results not only provide a new method for exploring stable helical molecules, but also provide a stepping stone for deciphering and modulating the charge-transport behavior of helical systems at the single-molecule level.
开发具有稳定螺旋结构的长链分子对于理解和调控螺旋生物大分子的性质和功能具有重要意义,但颇具挑战性。在这项工作中,提出了一种通过增强空间共轭来稳定折叠螺旋结构的有效且简便的方法,以新型邻位六亚苯基(o-HP)衍生物为模型。通过实验和理论研究了所制备的折叠螺旋o-HP衍生物的空间共轭与电荷传输行为之间的构效关系。结果表明,通过引入吸电子的吡啶和吡嗪环可以增强o-HP衍生物内部的空间共轭,从而有效稳定o-HP衍生物的螺旋结构。此外,扫描隧道显微镜-断结测量表明,o-HP衍生物稳定的规则螺旋结构开辟了主要的空间电荷传输途径,通过与吡啶和吡嗪增强空间共轭,单分子电导提高了70%以上。然而,通过化学键的电荷传输途径对o-HP衍生物电导的贡献要小得多。这些结果不仅为探索稳定的螺旋分子提供了一种新方法,也为在单分子水平上解读和调控螺旋体系的电荷传输行为提供了一块垫脚石。