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Robust Organic Radical Molecular Junctions Using Acetylene Terminated Groups for C-Au Bond Formation

机译:使用乙炔封端基团形成C-Au键的稳健有机自由基分子结

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摘要

Organic paramagnetic and electroactive molecules are attracting interest as core components of molecular electronic and spintronic devices. Currently, further progress is hindered by the modest stability and reproducibility of the molecule/electrode contact. We report the synthesis of a persistent organic radical bearing one and two terminal alkyne groups to form Au–C σ bonds. The formation and stability of self-assembled monolayers and the electron transport through single-molecule junctions at room temperature have been studied. The combined analysis of both systems demonstrates that this linker forms a robust covalent bond with gold and a better-defined contact when compared to traditional sulfur-based linkers. Density functional theory and quantum transport calculations support the experimental observation highlighting a reduced variability of conductance values for the C–Au based junction. Our findings advance the quest for robustness and reproducibility of devices based on electroactive molecules.
机译:作为分子电子和自旋电子设备的核心组件,有机顺磁和电活性分子引起了人们的兴趣。当前,分子/电极接触的适度稳定性和可再现性阻碍了进一步的发展。我们报告了带有一个和两个末端炔基的持久性有机自由基的合成,以形成Au–Cσ键。研究了自组装单分子膜的形成和稳定性以及在室温下电子通过单分子结的传输。两种系统的综合分析表明,与传统的基于硫的连接基相比,该连接基与金形成牢固的共价键,并具有更清晰的接触。密度泛函理论和量子输运计算支持了实验观察,突出了基于C–Au的结的电导值的降低的可变性。我们的发现推动了对基于电活性分子的设备的耐用性和可再现性的追求。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2018年第5期|1691-1696|共6页
  • 作者单位

    Department of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (ICMAB- CSIC) and CIBER-BBN, Campus de la Universitat Autònoma de Barcelona (UAB), 08193 Bellaterra, Spain;

    Kavli Institute of Nanoscience, Delft University of Technology, Lorentzweg 1, Delft 2628 CJ, The Netherlands;

    Nano-Bio Spectroscopy Group and European Theoretical Spectroscopy Facility (ETSF), Universidad del País Vasco (UPV/EHU), Avenida Tolosa 72, 20018 San Sebastian, Spain;

    National Physical Laboratory, Teddington TW11 0LW, United Kingdom;

    Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland,Russian Academy of Sciences A. N. Frumkin Institute of Physical Chemistry and Electrochemistry RAS, Leninskii pr. 31, Moscow, 119991, Russia;

    Department of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (ICMAB- CSIC) and CIBER-BBN, Campus de la Universitat Autònoma de Barcelona (UAB), 08193 Bellaterra, Spain;

    Department of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (ICMAB- CSIC) and CIBER-BBN, Campus de la Universitat Autònoma de Barcelona (UAB), 08193 Bellaterra, Spain;

    Department of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (ICMAB- CSIC) and CIBER-BBN, Campus de la Universitat Autònoma de Barcelona (UAB), 08193 Bellaterra, Spain;

    Kavli Institute of Nanoscience, Delft University of Technology, Lorentzweg 1, Delft 2628 CJ, The Netherlands;

    Department of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (ICMAB- CSIC) and CIBER-BBN, Campus de la Universitat Autònoma de Barcelona (UAB), 08193 Bellaterra, Spain;

    Kavli Institute of Nanoscience, Delft University of Technology, Lorentzweg 1, Delft 2628 CJ, The Netherlands,IMDEA Nanoscience, Ciudad Universitaria de Cantoblanco, c/Faraday 9, 28049 Madrid, Spain;

    Department of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (ICMAB- CSIC) and CIBER-BBN, Campus de la Universitat Autònoma de Barcelona (UAB), 08193 Bellaterra, Spain;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 入库时间 2022-08-18 03:07:18

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