电导
空格(标点符号)
纳米技术
化学
材料科学
化学物理
物理
计算机科学
凝聚态物理
操作系统
作者
Shaoshao Jiao,Pingchuan Shen,Jinshi Li,Xiaobin Dong,Wei He,Zujin Zhao
标识
DOI:10.1002/ange.202414801
摘要
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, 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. But 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 pave a stepping stone for deciphering and modulating the charge transport behavior of helical systems at the single‐molecule level.
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