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使用乙炔封端基团构建稳健的有机自由基分子结用于 C-Au 键形成。

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

机构信息

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.

出版信息

J Am Chem Soc. 2018 Feb 7;140(5):1691-1696. doi: 10.1021/jacs.7b10019. Epub 2018 Jan 25.

Abstract

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.

摘要

有机顺磁和电活性分子作为分子电子和自旋电子器件的核心组件引起了人们的兴趣。目前,分子/电极接触的稳定性和重现性较差,阻碍了进一步的发展。我们报告了一种含有一个和两个末端炔基的稳定有机自由基的合成,以形成 Au-C σ 键。在室温下研究了自组装单层的形成和稳定性以及通过单分子结的电子输运。对这两个系统的综合分析表明,与传统的基于硫的配体相比,这种连接物与金形成了牢固的共价键,并且形成了更明确的接触。密度泛函理论和量子输运计算支持实验观察,突出了基于 C-Au 结的电导值的可变性降低。我们的发现推进了基于电活性分子的器件的稳健性和重现性的研究。

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