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Viologen Tweezers to Probe the Force of Individual Donor-Acceptor π-Interactions

机译:viologen镊子探测单个供体受体π相互作用的力量

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摘要

Donor-acceptor (DA) π-interactions are weak attractive forces that are exploited widely in molecular and supramolecular chemistry. They have been characterized extensively by ensemble techniques, providing values for their energies that are useful for the design of soft materials. For implementation of motions or operations based on these DA π-interactions in wholly synthetic molecular machines, the mechanical strength and force associated with their out-of-equilibrium performance are the key parameters, in addition to their energies obtained at thermodynamic equilibrium. In this context, we have used single-molecule force spectroscopy as a nonequilibrium technique to determine the mechanical strength of individual DA π-interactions in solution. We designed and synthesized a molecular tweezer that is able to encapsulate π-donors and also demonstrated a precise opening extension. The mechanical breaking of the noncovalent interactions between viologen units-π-acceptors commonly employed in mechanically interlocked molecules-and several π-donors afforded a characteristic force-distance signature, revealing the opening of individual viologen tweezers with an unambiguous extension. Single-tweezer host-exchange experiments performed in situ demonstrated the sensitivity of the technique. This simple design could be exploited in quantifying the force of a large range of weak noncovalent bonding interactions as well as the potential work that molecular machines can generate at the single-molecule level.
机译:供体受体(DA)π相互作用是弱的吸引力,其在分子和超分子化学中广泛利用。它们通过集合技术进行了广泛的特征,为它们的能量提供了可用于设计软材料的能量的值。为了实现基于全完全合成的分子机中的基于这些DAπ相互作用的运动或操作,除了在热力学平衡时获得的能量之外,与其超平衡性能相关的机械强度和力是关键参数。在这种情况下,我们使用单分子力光谱作为非识别技术,以确定溶液中单个DEπ相互作用的机械强度。我们设计和合成了一种能够封装π-供体的分子镊子,并且还证明了精确的开口延伸。在机械互锁分子中通常采用的viologen单位 - π-受体之间的非共价相互作用的机械破碎 - 以及几个π-供体的特征力距离签名,揭示了具有明确延伸的个体Viologen镊子的开口。原位执行的单镊子主机交换实验证明了该技术的灵敏度。这种简单的设计可以在量化大范围的非共价键合相互作用以及分子机可以在单分子水平上产生的潜在工作来利用。

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  • 来源
    《Journal of the American Chemical Society》 |2020年第50期|21153-21159|共7页
  • 作者单位

    Research Unit MolSys NanoChem University of Liege Liege 4000 Belgium Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States Institute for Molecular Design and Synthesis Tianjin University Tianjin 300072 China School of Chemistry University of New South Wales Sydney New South Wales 2052 Australia;

    Research Unit MolSys NanoChem University of Liege Liege 4000 Belgium;

  • 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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  • 正文语种 eng
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