{"title":"Supramolecular Diodes with Donor–Acceptor Interactions","authors":"Wei Xu, Hua Zhang, Yu Zhou, Taige Lu, Yuting Li, Yixuan Zhu, Caiyun Wei, Jueting Zheng, Ruihao Li, Jing Li, Lijue Chen, Guanxin Zhang, Jia Shi, Junyang Liu, Deqing Zhang, Wenjing Hong","doi":"10.1021/jacs.4c14656","DOIUrl":null,"url":null,"abstract":"Inspired by the initial proposal of σ-bridged donor–acceptor (D-σ-A) single-molecule diodes in 1974, extensive studies over the past 50 years have explored various designs for π-conjugated D-π–A single-molecule diodes due to their feasible chemical synthesis and effective charge transfer. However, the rectification ratio of π-conjugated single-molecule diodes has been long-term limited by the challenge of asymmetric electronic coupling to induce the rectification effect. Here, we present a supramolecular diode constructed through an intramolecular π–π interaction-driven assembly strategy. The asymmetric transmission in this system is tunable via subangström mechanical control, resulting in a rectification ratio of up to 16. Electron transport studies reveal that this through-space D-π–π–A system constructed by the π–π stacking between pyrene (<b>Py</b>) and naphthalenediimide (<b>NDI</b>) is crucial for achieving asymmetric currents under different bias polarization. Theoretical calculations suggest that the intermolecular destructive quantum interference not only enables a sharp variation in electron transmission but also facilitates asymmetric electronic energy shifts through mechanical stretching, significantly improving the rectification ratio. Our work provides a general approach to fabricating and modulating asymmetric molecular architectures through noncovalent supramolecular interactions, showcasing the potential of high-performance single-molecule rectifiers.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"47 1","pages":""},"PeriodicalIF":14.4000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c14656","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Inspired by the initial proposal of σ-bridged donor–acceptor (D-σ-A) single-molecule diodes in 1974, extensive studies over the past 50 years have explored various designs for π-conjugated D-π–A single-molecule diodes due to their feasible chemical synthesis and effective charge transfer. However, the rectification ratio of π-conjugated single-molecule diodes has been long-term limited by the challenge of asymmetric electronic coupling to induce the rectification effect. Here, we present a supramolecular diode constructed through an intramolecular π–π interaction-driven assembly strategy. The asymmetric transmission in this system is tunable via subangström mechanical control, resulting in a rectification ratio of up to 16. Electron transport studies reveal that this through-space D-π–π–A system constructed by the π–π stacking between pyrene (Py) and naphthalenediimide (NDI) is crucial for achieving asymmetric currents under different bias polarization. Theoretical calculations suggest that the intermolecular destructive quantum interference not only enables a sharp variation in electron transmission but also facilitates asymmetric electronic energy shifts through mechanical stretching, significantly improving the rectification ratio. Our work provides a general approach to fabricating and modulating asymmetric molecular architectures through noncovalent supramolecular interactions, showcasing the potential of high-performance single-molecule rectifiers.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.