Azolylphenanthridine-ligated Cu(II) catalyst for electrochemical oxidation of cholesterol in aprotic medium

被引:0
|
作者
Okhokhonin, Andrei, V [1 ]
Akulov, Alexey A. [1 ]
Izmozherova, Yulia, V [1 ]
Pershin, Andrey A. [1 ]
Tsmokalyuk, Anton N. [1 ]
Svalova, Tatiana S. [1 ]
Sharutin, Vladimir V. [2 ]
Zyryanov, Grigory, V [1 ,3 ]
Chupakhin, Oleg N. [1 ,3 ]
Varaksin, Mikhail V. [1 ,3 ]
Kozitsina, Alisa N. [1 ]
机构
[1] Ural Fed Univ, 19 Mira Str, Ekaterinburg 620002, Russia
[2] South Ural State Univ, Natl Res Univ, 76 Lenina Ave, Chelyabinsk 454080, Russia
[3] Postovsky Inst Organ Synth, 22 S Kovalevskoy Str, Ekaterinburg 620990, Russia
基金
俄罗斯科学基金会;
关键词
N-HETEROCYCLIC CARBENE; PHENANTHRIDINE; COMPLEXES; CHEMISTRY;
D O I
10.1016/j.ica.2024.122305
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis of original 6-(azol-1-yl)phenanthridine ligands and a copper(II) complex based on them is reported. Comprehensive studies of the structural, physicochemical, and electrocatalytic properties for the selected 6-(1H-pyrazol-1-yl)phenanthridine-containing H-pyrazol-1-yl)phenanthridine-containing coordination compound have been carried out. The latter has demonstrated pronounced electrochemical and electrocatalytic activities in the enzyme-free cholesterol oxidation in DMSO. A six-stage mechanism including electrocatalytic reduction of cholesterol and subsequent oxidation of its reduction products has been proposed and underpinned by quantum mechanical considerations. Obtained analytical characteristics of the enzyme-free cholesterol oxidation (LoD 0.0032 mM, detectable concentrations 0.01-0.40 mM) open a prospect towards the investigated complexes to be applied as sensitive elements of portable electrochemical platforms for the point-of-care diagnostics.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Electrochemical impedance analysis of urea electro-oxidation mechanism on nickel catalyst in alkaline medium
    Guo, Fen
    Ye, Ke
    Du, Mengmeng
    Huang, Xiaomei
    Cheng, Kui
    Wang, Guiling
    Cao, Dianxue
    ELECTROCHIMICA ACTA, 2016, 210 : 474 - 482
  • [22] ELECTROCHEMICAL OXIDATION OF MN(II) TO MNO4- IN THE PRESENCE OF AG(I) CATALYST
    COMNINELLIS, C
    PETITPIERRE, JP
    ELECTROCHIMICA ACTA, 1991, 36 (08) : 1363 - 1365
  • [23] Chemical and electrochemical water oxidation mediated by bis(pyrazol-1-ylmethyl)pyridine-ligated Cu(i) complexes
    Makhado, T.
    Das, B.
    Kriek, R. J.
    Vosloo, H. C. M.
    Swarts, A. J.
    SUSTAINABLE ENERGY & FUELS, 2021, 5 (10) : 2771 - 2780
  • [24] Electrochemical monitoring of methylparathion degradation inn an acid aqueous medium in presence of Cu(II)
    Manzanilla-Cano, JA
    Barceló-Quintal, MH
    Reyes-Salas, EO
    JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART B-PESTICIDES FOOD CONTAMINANTS AND AGRICULTURAL WASTES, 2004, 39 (04) : 577 - 588
  • [25] Enantioselective allylic oxidation of cycloalkenes by using Cu(II)-tris(oxazoline) complex as a catalyst
    Kawasaki, K
    Katsuki, T
    TETRAHEDRON, 1997, 53 (18) : 6337 - 6350
  • [27] Catalytic activity of bimetallic catalyst Pd(II)(PVP)-Cu(II)(PVP) in oxidation of octene-1
    Akbayeva, D. N.
    Bakirova, B. S.
    Smagulova, I. A.
    Rsaldina, D. E.
    MATERIALS TODAY-PROCEEDINGS, 2020, 31 : 572 - 575
  • [28] Dual Matrix Influence on Ni(II) Rich Hybrid Catalyst for Electrochemical Methanol Oxidation Reaction
    Hoque, Nazimul
    Lee, Seonghwan
    Park, Young-Bin
    Roy, Subhasish
    Baruah, Manash J.
    Biswas, Subir
    Gogoi, Gautam
    Bora, Tonmoy J.
    Dutta, Rupjyoti
    Bania, Kusum K.
    CHEMNANOMAT, 2022, 8 (10)
  • [29] Saccharide derived dinuclear Cu(II) complex: An efficient catalyst for oxidation of catechol and benzylic alcohols
    Soni, Kiran
    Kumar, Anil
    Sah, Ajay K.
    CATALYSIS COMMUNICATIONS, 2012, 17 : 95 - 98
  • [30] Selective Oxidation of n-Hexane by Cu (II) Nanoclusters Supported on Nanocrystalline Zirconia Catalyst
    Acharyya, Shankha Shubhra
    Ghosh, Shilpi
    Adak, Shubhadeep
    Singh, Raghuvir
    Saran, Sandeep
    Bal, Rajaram
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2015, 15 (08) : 5816 - 5822