电化学发光
化学
纳米团簇
等温滴定量热法
非金属
猝灭(荧光)
过氧二硫酸盐
接受者
脱氧核糖核酸
化学发光
电子
密度泛函理论
检出限
电子受体
合理设计
电子转移
纳米技术
能量转移
三噻吩
光化学
热化学
激发态
自电离
设计要素和原则
光电子学
电子供体
组合化学
作者
Zhongnan Huang,Qinhui Lin,Yaling Chen,Yuxing Lei,Zhenglian Li,Yunzhong Xu,Wei Chen,Hua‐Ping Peng
标识
DOI:10.1021/acs.analchem.5c05612
摘要
Monitoring the levels and metabolic changes of deoxyribonucleotides is crucial for various clinical disease research studies. In this study, we propose a highly efficient nonmetal material self-mediated electron transfer (ET)-based electrochemiluminescence (ECL) sensing platform. This platform utilizes deoxyguanosine monophosphate (dGMP) as a model nonmetal-based electron acceptor and strategically employs 6-aza-2-thiothymine-protected gold nanoclusters (ATT-AuNCs) with matched energy levels as the ECL donor. The ET-mediated quenching mechanism has been investigated using ECL technology, isothermal titration calorimetry measurements, and density functional theory (DFT) calculations. These investigations reveal that dGMP is uniquely capable of undergoing spontaneous ET with ATT-AuNCs compared with the other three deoxyribonucleotides (dAMP, dTMP, and dCMP). Furthermore, dGMP exhibits the lowest reorganization energy (λ) after ET, indicating superior ET kinetics, which results in more efficient ECL quenching and excellent detection selectivity. The achieved detection limit is as low as 2.7 × 10-12 M, significantly outperforming most reported methodologies. Additionally, the proposed ET-ECL sensing platform demonstrates notable advantages, including high efficiency, simplicity, exceptional sensitivity, and excellent specificity. Consequently, this study establishes a new paradigm for studying nonmetal-mediated ET-based ECL mechanisms and provides a foundation for future high-performance sensing systems based on molecular ET behavior.
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