1985
DOI: 10.1039/c39850000370
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Controlled growth of poly(N-vinylcarbazole) films on Pt by scan technique electropolymerization of N-vinylcarbazole

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Cited by 20 publications
(20 citation statements)
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“…The preparation of poly(N-vinylcarbazole) (PVCz) by electrochemical polymerization has been known for many years [1][2][3][4]. The first stage of electropolymerization involves the oxidation of monomer to the cation radical.…”
Section: Introductionmentioning
confidence: 99%
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“…The preparation of poly(N-vinylcarbazole) (PVCz) by electrochemical polymerization has been known for many years [1][2][3][4]. The first stage of electropolymerization involves the oxidation of monomer to the cation radical.…”
Section: Introductionmentioning
confidence: 99%
“…Only a few papers have described the electrodeposition of films from carbazole and their properties [15][16][17]. On the other hand, the anodic oxidation of N-ethyl carbazole (ECz) in acetonitrile does not produce films [15] except on Au and glassy carbon electrodes in aqueous HClO 4 with conductivities of between 10 Ϫ 8 and 10 Ϫ 4 S/cm [18]. As noted above the oxidative polymerization of carbazoles by using metal salts have not been investigated systematically so far.…”
Section: Introductionmentioning
confidence: 99%
“…The electrochemical polymerization of NVK proceeds through an electrochemical-chemical-electrochemical mechanism [23][24][25][26] (Scheme 1), which starts with the oxidation of the monomer to the corresponding cation radical (1 → 2) followed by a fast dimerization at position 3 of the carbazole unit (2 → 3). The two-electron oxidation 3 → 4, which occurs at less positive potential than that required for the oxidation of the monomer, leads to the formation of a dimer bonded between the carbazole units (4).…”
Section: Introductionmentioning
confidence: 99%
“…When dimerization occurs, H + ions split off and provoke the polymerization of NVK through its vinyl group. The attack of these protons (H + ) to the vinyl group of the growing electron-conducting polymer (4 → 5), causes cross-linking (5 → 6), whereas the activation of the vinyl group of the monomer in solution leads to the formation of a photo-conducting polymer (structure 8, Scheme 2) [23][24][25][26]. The deposited poly(3,6-N -vinylcarbazole) formed on the anode surface, here named P3,6NVK, exhibits different cross-linking degrees (m in structure 6, Scheme 1) depending on the synthesis conditions.…”
Section: Introductionmentioning
confidence: 99%
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