增强Cu(II)介导的Chan-Lam偶联的选择性和约束,用于建立即时诊断

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY ChemElectroChem Pub Date : 2025-03-26 DOI:10.1002/celc.202400642
Yu-Chia Chang, Prof. Kevin D. Moeller
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摘要

Cu(II) 介导的 Chan-Lam 偶联反应为开发微电极阵列上的床旁检测设备提供了多种益处。然而,由于本底反应的存在,在基于硼酸酯的聚合物表面实现选择性被证明是困难的。我们使用荧光标记的乙炔亲核物进行了基于荧光的研究。最初的实验发现,整个电极阵列都有明显的本底荧光,这表明存在选择性问题。进一步的调查发现,即使没有铜,也会发生明显的背景反应。为了解决这个问题,我们开发了一种利用芳基溴化聚合物的策略,通过最大限度地减少背景非特异性反应来提高反应的选择性。对限制机制的探索揭示了乙炔在形成二聚体中的作用,从而促进了从所使用的特定电极中逸出的铜(II)试剂的快速消耗。这些发现为构建用于代谢物多重护理点检测的设备提供了一种方法,从而提高了诊断设备的性能和准确性。
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Enhancing the Selectivity and Confinement of the Cu(II)-Mediated Chan-Lam Coupling for Use in Building Point-of-Care Diagnostics

The Cu(II)-mediated Chan-Lam coupling reaction offers several benefits for developing point-of-care detection devices on microelectrode arrays. However, achieving selectivity on borate ester-based polymer surfaces has proven difficult due to background reactions. Fluorescence-based studies were conducted using fluorescently labeled acetylene nucleophiles. Initial experiments revealed significant background fluorescence across the electrode array, indicating selectivity issues. Further investigation uncovered significant background reactions occurring even without copper. To address this, a strategy utilizing an arylbromide-based polymer was developed, enhancing reaction selectivity by minimizing background non-specific reactions. Exploration into the confinement mechanism revealed the role of acetylene in forming dimers, facilitating rapid consumption of Cu(II) reagents that escaped from the specific electrodes used. These findings offer a way to construct devices for the multiplex point-of-care detection of metabolites, improving performance and accuracy in diagnostic devices.

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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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