A Dinitrophenol-Based Colorimetric Chemosensor for Sequential Cu2+ and S2- Detection

被引:10
|
作者
Nam, Hyejin [1 ]
Moon, Sungjin [1 ]
Gil, Dongkyun [1 ]
Kim, Cheal [1 ]
机构
[1] Seoul Natl Univ Sci & Technol SNUT, Dept Fine Chem & Renewable Energy Convergence, Seoul 01098, South Korea
基金
新加坡国家研究基金会;
关键词
dinitrophenol; colorimetric chemosensor; Cu2+; S2-; DFT calculation; FLUORESCENT CHEMOSENSOR; HYDROGEN-SULFIDE; AQUEOUS-MEDIA; WATER; PROBE; IONS; RECOGNITION; COMPLEX; CO2+;
D O I
10.3390/chemosensors11020143
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A dinitrophenol-based colorimetric chemosensor sequentially sensing Cu2+ and S2-, HDHT ((E)-2-(2-(2-hydroxy-3,5-dinitrobenzylidene)hydrazineyl)-N,N,N-trimethyl-2-oxoethan-1-aminium), was designed and synthesized. The HDHT selectively detected Cu2+ through a color change of yellow to colorless. The calculated detection limit of the HDHT for Cu2+ was 6.4 x 10(-2) mu M. In the interference test, the HDHT was not considerably inhibited by various metal ions in its detection of Cu2+. The chelation ratio of the HDHT to Cu2+ was determined as 1:1 by using a Job plot and ESI-MS experiment. In addition, the HDHT-Cu2+ complex showed that its color selectively returned to yellow only in the presence of S2-. The detection limit of the HDHT-Cu2+ complex for S2- was calculated to be 1.2 x 10(-1) mu M. In the inhibition experiment for S2-, the HDHT-Cu2+ complex did not significantly interfere with other anions. In the real water-sample test, the detection performance of the HDHT for Cu2+ and S2- was successfully examined. The detection features of HDHT for Cu2+ and the HDHT-Cu2+ for S2- were suggested by the Job plot, UV-Vis, ESI-MS, FT-IR spectroscopy, and DFT calculations.
引用
收藏
页数:15
相关论文
共 50 条
  • [1] A simple colorimetric chemosensor for relay detection of Cu2+ and S2- in aqueous solution
    Kim, Min Seon
    Jung, Jae Min
    Ahn, Hye Mi
    Kim, Cheal
    [J]. JOURNAL OF COORDINATION CHEMISTRY, 2018, 71 (02) : 355 - 370
  • [2] Colorimetric Detection of Cu2+ and Fluorescent Detection of PO43- and S2- by a Multifunctional Chemosensor
    Joo, Dong Hee
    Mok, Jin Su
    Bae, Geon Hwan
    Oh, Sang Eun
    Kang, Ji Hye
    Kim, Cheal
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2017, 56 (30) : 8399 - 8407
  • [3] Colorimetric chemosensor for multiple targets, Cu2+, CN- and S2-
    Ryu, Ka Young
    Lee, Jae Jun
    Kim, Jin Ah
    Park, Dae Yul
    Kim, Cheal
    [J]. RSC ADVANCES, 2016, 6 (20) : 16586 - 16597
  • [4] Colorimetric detection of Cu2+ by amino phenol based chemosensor
    Patil, D. Y.
    Khadke, N. B.
    Patil, A. A.
    Borhade, A. V.
    [J]. RESULTS IN CHEMISTRY, 2022, 4
  • [5] A benzyl carbazate-based colorimetric chemosensor for relay detection of Cu2+ and S2- in near-perfect aqueous media
    Park, Soyoung
    Choe, Donghwan
    Lee, Jae Jun
    Kim, Cheal
    [J]. JOURNAL OF MOLECULAR STRUCTURE, 2021, 1240
  • [6] A single chemosensor for the detection of dual analytes Cu2+ and S2- in aqueous media
    Park, Dae Yul
    Ryu, Ka Young
    Kim, Jin Ah
    Kim, So Young
    Kim, Cheal
    [J]. TETRAHEDRON, 2016, 72 (27-28) : 3930 - 3938
  • [7] An anthraquinone-based highly selective colorimetric and fluorometric sensor for sequential detection of Cu2+ and S2- with intracellular application
    Hou, Lingjie
    Kong, Xiangyu
    Wang, Yishou
    Chao, Jianbin
    Li, Chenzhong
    Dong, Chuan
    Wang, Yu
    Shuang, Shaomin
    [J]. JOURNAL OF MATERIALS CHEMISTRY B, 2017, 5 (45) : 8957 - 8966
  • [8] A thiol-containing colorimetric chemosensor for relay recognition of Cu2+ and S2- in aqueous media with a low detection limit
    So, Haeri
    Chae, Ju Byeong
    Kim, Cheal
    [J]. INORGANICA CHIMICA ACTA, 2019, 492 : 83 - 90
  • [9] Amino-Quinoline Based Colorimetric Chemosensor for Cu2+ Detection
    Patil, D. Y.
    Khadke, N. B.
    Patil, A. A.
    Borhade, A., V
    [J]. JOURNAL OF ANALYTICAL CHEMISTRY, 2022, 77 (01) : 18 - 25
  • [10] Amino-Quinoline Based Colorimetric Chemosensor for Cu2+ Detection
    D. Y. Patil
    N. B. Khadke
    A. A. Patil
    A. V. Borhade
    [J]. Journal of Analytical Chemistry, 2022, 77 : 18 - 25