快速交变极性作为合成电化学的独特工具

IF 0.2 4区 化学 Q4 CHEMISTRY, ORGANIC Journal of Synthetic Organic Chemistry Japan Pub Date : 2023-11-01 DOI:10.5059/yukigoseikyokaishi.81.1020
Yu Kawamata, Phil S. Baran
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引用次数: 0

摘要

由可再生能源驱动的电合成是一种以可持续的方式获得有用化学反应性的有力方法。通常,电化学反应是使用直流电(DC)进行的,其中电子沿单一方向流动。相比之下,尽管交流电在我们的日常生活中得到了广泛的应用,但它在合成电化学领域的应用还很少。这可能源于对使用这种波形缺乏独特反应性/选择性的历史认知,以及缺乏现成的仪器来消除大规模采用的工程障碍。该领域的一个突破是引入了快速交替极性(rAP),它可以在毫秒时间尺度内交替电极的极性。这种电流传递模式现已在广泛使用的恒电位器ElectraSyn2.0中实现,可以在有机合成中获得独特的反应性和选择性,这是目前任何已知方法(化学或电化学)都无法实现的。rAP具有显著的化学选择性和简单性,为现代合成电化学开辟了新的前景。
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Rapid Alternating Polarity as a Unique Tool for Synthetic Electrochemistry
Electrosynthesis, driven by renewable energy, is a powerful method for accessing useful chemical reactivity in a sustainable fashion. Typically, electrochemical reactions have been carried out using direct current (DC), where electrons flow in a single direction. In contrast, utilization of alternating current (AC) has been largely unexplored in synthetic electrochemistry despite its wide applications in our daily life. This could stem from a historical perception regarding the lack of unique reactivity/selectivity that would result from using such a waveform, as well as the absence of readily available instrumentation to remove the engineering barrier for mass adoption. A breakthrough in this area is the introduction of rapid alternating polarity (rAP), which alternates the polarity of an electrode in the millisecond timescale. This mode of current delivery, now implemented in the widely employed potentiostat, ElectraSyn2.0, enables access to unique reactivity and selectivity in organic synthesis that are challenging or currently impossible to achieve by any known method (chemical or electrochemical). The remarkable chemoselectivity and simplicity of rAP open new vistas in modern synthetic electrochemistry.
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来源期刊
CiteScore
0.30
自引率
0.00%
发文量
120
审稿时长
6-12 weeks
期刊介绍: Information not localized
期刊最新文献
Synthetic Element Chemistry based on Precise Designs of Reagents and Transition States Use of Emerging C-H Functionalization Methods to Implement Strategies for the Divergent Total Syntheses of Bridged Polycyclic Natural Products Rapid Alternating Polarity as a Unique Tool for Synthetic Electrochemistry Synthesis of Structurally Diverse Polycyclic Arenes Using Tandem Oxidative Ring Expansion Strategy Divergent Transformation of Carboxylic Acids through Photocatalytic Decarboxylation with Hypervalent Iodine Reagents
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