In Situ Formed 3,3′,5,5′-Tetramethylbenzidine-Cu(I/II) Charge-Transfer Complex Intermediates Promoting Colorimetric Assay of Cr6+

被引:0
|
作者
Zhao, Jiahui [1 ]
Zhao, Yixuan [1 ]
Shao, Xuefeng [1 ]
Sun, Ying [1 ]
Wen, Huang [2 ,3 ]
Liu, Jian [1 ]
机构
[1] Jiangxi Normal Univ, Coll Chem Engn, Sch Chem Engn, State Prov Joint Engn Lab Zeolite Membrane Mat, Nanchang 330022, Peoples R China
[2] Putian Univ, Sch Pharm & Med Technol, Key Lab Pharmaceut Anal, Putian 351100, Peoples R China
[3] Putian Univ, Lab Med Fujian Prov, Putian 351100, Peoples R China
基金
中国国家自然科学基金;
关键词
FENTON-LIKE SYSTEMS; HEXAVALENT CHROMIUM; HYDROGEN-PEROXIDE; OXIDATION; REDUCTION; H2O2; ACTIVATION;
D O I
10.1021/acs.inorgchem.4c02619
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Developing a synthesis-free, multifunctional, and effective colorimetric assay system based on 3,3 ',5,5 '-tetramethylbenzidine (TMB) oxidation is attractive yet challenging. Herein, we established a synergetic Cu2+/Cr6+-promoting strategy for TMB-based colorimetric detection of Cr6+. By introducing Cu2+, critical TMB center dot(+)center dot center dot center dot Cu(I/II)center dot center dot center dot TMB charge transfer complex (TMC) intermediates were in situ formed to reduce the activation energy of TMB oxidation, thereby accelerating Cr6+-mediated TMB oxidation. TMC intermediates also played a pivotal role in H2O2-participated TMB oxidation, clarifying the secondary responsibility of reactive oxygen species frequently caused by Fenton-like reactions. Leveraging the synergetic capacity between Cu2+ and Cr6+ for TMB oxidation, we demonstrated sensitive and specific colorimetric detections for Cr6+ with a limit of detection of 0.006 mu M. With its convenient operation and rapid responsiveness, this strategy successfully enabled the practical detection of Cr6+ in real water samples. This work not only enhances the understanding of the internal acceleration mechanism in colorimetric sensing but also provides valuable opportunities to advance synthesis-free detection platforms.
引用
收藏
页码:17005 / 17013
页数:9
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