Cadmium-sensitive electrode based on tetracetone derivatives of p-tert-butylcalix[8]arene

被引:17
作者
Dernane, C. [1 ]
Zazoua, A. [1 ]
Kazane, I. [1 ]
Jaffrezic-Renault, N. [2 ]
机构
[1] Univ Jijel, Lab Mat Elaborat Proprietes Applicat, Ouled Aissa 18000, Jijel, Algeria
[2] Univ Lyon 1, LSA UMR CNRS 5180, F-69622 Villeurbanne, France
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2013年 / 33卷 / 07期
关键词
Calix[8]arene; Cadmium-sensitive electrode; Impedance spectroscopy; Sensors; ISFET SENSORS; ION DETECTION; THIN-FILMS; CALIXARENE; SPECTROMETRY; CHEMOSENSOR; FLUORESCENT; MERCURY(II); MEMBRANE; PROSTATE;
D O I
10.1016/j.msec.2013.04.049
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The performance of a cadmium-sensitive electrode based on the tetracetone derivatives of p-tert butylcalix [8]arene was investigated. The ion-sensitivity of the calix[8]arene was examined via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), X-ray photoelectron spectrometry, UV/Vis spectroscopy and FT-IR spectroscopy. The sensitive membrane containing the active ionophore was cast onto the surface of a gold electrode. The electrode exhibited a linear relationship between the charge transfer resistance (R-ct) and the logarithm of the detected ion concentration. The cathodic peak at a potential of 0.56 V increased linearly as the Cd2+ ion concentration increased. The detection limit of the device reached 10(-7) M with high sensitivity toward cadmium. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:3638 / 3643
页数:6
相关论文
共 50 条
[41]   Adsorption of direct black-38 azo dye on p-tert-butylcalix[6]arene immobilized material [J].
Kamboh, Muhammad Afzal ;
Bhatti, Asif Ali ;
Solangi, Imam Bakhsh ;
Sherazi, S. T. H. ;
Memon, Shahabuddin .
ARABIAN JOURNAL OF CHEMISTRY, 2014, 7 (01) :125-131
[42]   An excellent arsenic(V) sorption behavior of p-tert-butylcalix[8]areneoctamide impregnated resin [J].
Qureshi, Imdadullah ;
Memon, Shahabuddin ;
Yilmaz, Mustafa .
COMPTES RENDUS CHIMIE, 2010, 13 (11) :1416-1423
[43]   Linear and crosslinked copolymers of p-tert-butylcalix[4]arene derivatives and styrene:: New synthetic approaches to polymer-bound calix[4]arenes [J].
Mendes, AR ;
Gregório, CC ;
Barata, PD ;
Costa, AI ;
Prata, JV .
REACTIVE & FUNCTIONAL POLYMERS, 2005, 65 (1-2) :9-21
[44]   Recovery of host crystals from inclusion crystals of p-tert-butylcalix[4]arene and p-tert-butylthiacalix[4]arene by the treatment with a solvent and/or supercritical CO2 [J].
Morohashi, Naoya ;
Ebata, Kohei ;
Hattori, Tetsutaro .
JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 2018, 90 (3-4) :279-285
[45]   Synthesis and Crystal Structure of p-tert-Butylcalix[4]arene 1,3-Distal and Monosubstituted Semicarbazones and Thiosemicarbazones [J].
Liu Zhenming ;
Liu Dongmei ;
Wang Jinxiang ;
Sun Jing ;
Yan Chaoguo .
CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2014, 30 (03) :415-419
[46]   Extraction and DFT study on the complexation of H3O+ with hexaethyl p-tert-butylcalix[6]arene hexaacetate [J].
Lang, Jan ;
Dybal, Jiri ;
Makrlik, Emanuel ;
Vanura, Petr ;
Vasickova, Sona ;
Malon, Petr .
JOURNAL OF MOLECULAR STRUCTURE, 2007, 846 (1-3) :157-160
[47]   Synthesis and crystal structure of p-tert-butylcalix[4]arene 1,3-distal and monosubstituted semicarbazones and thiosemicarbazones [J].
Zhenming Liu ;
Dongmei Liu ;
Jinxiang Wang ;
Jing Sun ;
Chaoguo Yan .
Chemical Research in Chinese Universities, 2014, 30 :415-419
[48]   Dicopper complex of p-tert-butylcalix8arene bearing acylhydrazone pendant domains [J].
Yan, Chao-Guo ;
Han, Jun ;
Li, Liang ;
Liu, Dong-Mei .
JOURNAL OF COORDINATION CHEMISTRY, 2009, 62 (05) :825-832
[49]   Catalytic application of zinc complex of oxygen depleted 1,3-bis(pyrazole)-p-tert-butylcalix[4]arene [J].
Sinha, Anshu Kumar ;
Vigalok, Arkadi ;
Rawat, Varun .
TETRAHEDRON LETTERS, 2019, 60 (11) :796-799
[50]   Hydrogen-bonded hexameric cluster of benzyl alcohol in the solid state polymeric organization of p-tert-Butylcalix[5]arene [J].
Kajiki, Yasunori ;
Sekiya, Ryo ;
Haino, Takeharu .
SUPRAMOLECULAR CHEMISTRY, 2016, 28 (5-6) :444-449