2005
DOI: 10.1016/j.jelechem.2005.04.001
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Electrochemical and morphological characterization of poly[(R)-(−)-3-(l-pyrrolyl)propyl-N-(3,5-dinitrobenzoyl)-α-phenylglycinate] films deposited on ITO electrodes

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Cited by 12 publications
(4 citation statements)
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“…However, the response peak for glucose of Pd NPs/SWCNT electrode (3 mC of charge deposition) was shifted to À0.15 V. It is due to the difference in electrode morphology that occurs during the growth of Pd nanoparticle layers. The similar result was reported in previous research [47]. The measured current of the Pd NPs/SWCNT electrode to 5 mM glucose was 129.9 mA (line b).…”
Section: à2supporting
confidence: 90%
“…However, the response peak for glucose of Pd NPs/SWCNT electrode (3 mC of charge deposition) was shifted to À0.15 V. It is due to the difference in electrode morphology that occurs during the growth of Pd nanoparticle layers. The similar result was reported in previous research [47]. The measured current of the Pd NPs/SWCNT electrode to 5 mM glucose was 129.9 mA (line b).…”
Section: à2supporting
confidence: 90%
“…Electropolymerization of thiophene-, , pyrrole-, and carbazole-based , monomers has been extensively studied due to the interesting properties of the resulting conducting polymer (CP) films, e.g., their electrochromic behavior. Electrochemical oxidative coupling of carbazole was first described by Ambrose and Nelson . Applying oxidative potentials, cation radicals are initially generated.…”
Section: Resultsmentioning
confidence: 99%
“…The six carbazole-based monomers were purchased from commercial suppliers or synthesized by us (see the Supporting Information). In our experiments, monomers with two, three, and four carbazole substituents have been used: Electropolymerization of thiophene-, 20,21 pyrrole-, 22 and carbazole-based 23,24 monomers has been extensively studied due to the interesting properties of the resulting conducting polymer (CP) films, e.g., their electrochromic behavior. 25−27 Electrochemical oxidative coupling of carbazole was first described by Ambrose and Nelson.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…Therefore, the properties can be adjusted by modification of the monomer structure by attaching different functional groups, such as, electron-donating and/or electronwithdrawing, n-dopable, or fluorescent substituents [10][11][12][13]. For instance, the appendage of a nitro group on the monomer structure would make the resulting polymers amenable for use in sensors or electrochemical capacitors [14,15].…”
Section: Introductionmentioning
confidence: 99%