Electric Field-Induced Sequential Prototropic Tautomerism in Enzyme-like Nanopocket Created by Single Molecular Break Junction.

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2024-12-25 Epub Date: 2024-11-04 DOI:10.1021/jacs.4c12423
P A Sreelakshmi, Rahul Mahashaya, Susanne Leitherer, Umar Rashid, Joseph M Hamill, Manivarna Nair, Pachaiyappan Rajamalli, Veerabhadrarao Kaliginedi
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Abstract

Mastering the control of external stimuli-induced chemical transformations with detailed insights into the mechanistic pathway is the key for developing efficient synthetic strategies and designing functional molecular systems. Enzymes, the most potent biological catalysts, efficiently utilize their built-in electric field to catalyze and control complex chemical reactions within the active site. Herein, we have demonstrated the interfacial electric field-induced prototropic tautomerization reaction in acylhydrazone entities by creating an enzymatic-like nanopocket within the atomically sharp gold electrodes using a mechanically controlled break junction (MCBJ) technique. In addition to that, the molecular system used here contains two coupled acylhydrazone reaction centers, hence demonstrating a cooperative stepwise electric field-induced reaction realized at the single molecular level. Furthermore, the mechanistic studies revealed a proton relay-assisted tautomerization showing the importance of external factors such as solvent in such electric field-driven reactions. Finally, single-molecule charge transport and energetics calculations of different molecular species at various applied electric fields using a polarizable continuum solvent model confirm and support our experimental findings. Thus, this study demonstrates that mimicking an enzymatic pocket using a single molecular junction's interfacial electric field as a trigger for chemical reactions can open new avenues to the field of synthetic chemistry.

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电场诱导单分子断裂交界处产生的酶样纳米口袋中的顺序原向同分异构体。
掌握外部刺激诱导化学转化的控制方法并详细了解其机理途径,是开发高效合成策略和设计功能分子系统的关键。酶是最有效的生物催化剂,能有效利用其内置电场催化和控制活性位点内的复杂化学反应。在这里,我们利用机械控制断裂结(MCBJ)技术,在原子锋利的金电极内创建了一个类似于酶的纳米插槽,从而证明了界面电场诱导的酰基腙实体原向同分异构反应。此外,本文使用的分子体系还包含两个耦合的酰基腙反应中心,从而展示了在单分子水平上实现的合作分步电场诱导反应。此外,机理研究还揭示了质子中继辅助的同分异构现象,显示了溶剂等外部因素在此类电场驱动反应中的重要性。最后,利用可极化连续介质模型对不同分子物种在不同外加电场下的单分子电荷传输和能量计算证实并支持了我们的实验发现。因此,这项研究表明,利用单分子交界处的界面电场模拟酶袋作为化学反应的触发器,可以为合成化学领域开辟新的途径。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
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.
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