Electrochemical Mechanism for the Preparation of Fe-Si Alloys by Melts Electrodeposition

2019 ◽  
Vol 18 (2) ◽  
Author(s):  
Hui Li ◽  
Dongbin Wang ◽  
Jing-long Liang ◽  
Hong-yan Yan ◽  
Zong-ying Cai ◽  
...  
Keyword(s):  
Cyclic Voltammetry ◽  
Electrochemical Method ◽  
Deposition Time ◽  
Experimental Results ◽  
Reaction Process ◽  
Thermodynamic Calculations ◽  
Pt Electrode ◽  
One Step ◽  
Electrochemical Mechanism ◽  
Cyclic Voltammetry Data

Abstract The melts dissolution characteristics and reaction process during the preparation of Fe-Si alloys by the melts electrochemical method were studied. The thermodynamic calculations and experimental results showed that the solubility of SiO2 in KCl-NaCl-NaF melts was 0.24 mas% at 1073 K. The cyclic voltammetry data showed that the reduction of SiO2 on a Pt electrode was a one-step electron process; when SiO2 accounted for 0.24 mas% of the NaCl-KCl-NaF melts, the Fe-Si alloy was prepared by electrodeposition at 1073 K. When the deposition time was 30 min, Fe3Si was formed.

scholarly journals Electrochemical Bromination of Glycals

2021 ◽  
Vol 9 ◽  
Author(s):  
Zhao-Xiang Luo ◽  
Miao Liu ◽  
Tian Li ◽  
De-Cai Xiong ◽  
Xin-Shan Ye
Keyword(s):  
Cyclic Voltammetry ◽  
High Efficiency ◽  
Reaction Process ◽  
Metal Catalyst ◽  
Sonogashira Coupling ◽  
Reaction Conditions ◽  
Radical Trapping ◽  
Protective Groups ◽  
Ferrier Rearrangement ◽  
One Step

Herein, the convenient one-step electrochemical bromination of glycals using Bu4NBr as the brominating source under metal-catalyst-free and oxidant-free reaction conditions was described. A series of 2-bromoglycals bearing different electron-withdrawing or electron-donating protective groups were successfully synthesized in moderate to excellent yields. The coupling of tri-O-benzyl-2-bromogalactal with phenylacetylene, potassium phenyltrifluoroborate, or a 6-OH acceptor was achieved to afford 2C-branched carbohydrates and disaccharides via Sonogashira coupling, Suzuki coupling, and Ferrier rearrangement reactions with high efficiency. The radical trapping and cyclic voltammetry experiments indicated that bromine radicals may be involved in the reaction process.

On the electroreduction mechanism of halobenzenes: Detection of intermediates in reduction of monohalobenzenes

1989 ◽  
Vol 54 (4) ◽  
pp. 900-910 ◽  
Author(s):  
Juan Casado ◽  
Iluminada Gallardo
Keyword(s):  
Cyclic Voltammetry ◽  
Electrochemical Behaviour ◽  
Experimental Results ◽  
Disk Electrode ◽  
Rotating Ring Disk Electrode ◽  
Mercury Cathode

Experimental results from electrochemical behaviour of halobenzenes in DMF at a mercury cathode are used to discuss alternative mechanisms of reduction. Intermediates of these mechanisms, such as phenyl anion, phenylmercury radical and phenylmercury cation have been detected at the electrode by using cyclic voltammetry and a rotating ring-disk electrode.

Redox Potential - (Electronic) Structure Relationships in 18- and 17-Electron Mononitrile (or Monocarbonyl) Diphosphine Complexes of Re and Fe

2001 ◽  
Vol 66 (1) ◽  
pp. 139-154 ◽  
Author(s):  
M. Fátima C. Guedes Da Silva ◽  
Luísa M. D. R. S. Martins ◽  
João J. R. Fraústo Da Silva ◽  
Armando J. L. Pombeiro
Keyword(s):  
Cyclic Voltammetry ◽  
Electronic Structure ◽  
Binding Sites ◽  
Closed Shell ◽  
Carbonyl Complexes ◽  
Metal Centre ◽  
Pt Electrode ◽  
Metal Site ◽  
Oxidation Potentials ◽  
First Time

The organonitrile or carbonyl complexes cis-[ReCl(RCN)(dppe)2] (1) (R = 4-Et2NC6H4 (1a), 4-MeOC6H4 (1b), 4-MeC6H4 (1c), C6H5 (1d), 4-FC6H4 (1e), 4-ClC6H4 (1f), 4-O2NC6H4 (1g), 4-ClC6H4CH2 (1h), t-Bu (1i); dppe = Ph2PCH2CH2PPh2), or cis-[ReCl(CO)(dppe)2] (2), as well as trans-[FeBr(RCN)(depe)2]BF4 (3) (R = 4-MeOC6H4 (3a), 4-MeC6H4 (3b), C6H5 (3c), 4-FC6H4 (3d), 4-O2NC6H4 (3e), Me (3f), Et (3g), 4-MeOC6H4CH2 (3h); depe = Et2PCH2CH2PEt2), novel trans-[FeBr(CO)(depe)2]BF4 (4) and trans-[FeBr2(depe)2] (5) undergo, as revealed by cyclic voltammetry at a Pt-electrode and in aprotic non-aqueous medium, two consecutive reversible or partly reversible one-electron oxidations assigned as ReI → ReII → ReIII or FeII → FeIII → FeIV. The corresponding values of the oxidation potentials IE1/2ox and IIE1/2ox (waves I and II, respectively) correlate with the Pickett's and Lever's electrochemical ligand and metal site parameters. This allows to estimate these parameters for the various nitrile ligands, depe and binding sites (for the first time for a FeIII/IV couple). The electrochemical ligand parameter show dependence on the "electron-richness" of the metal centre. The values of IE1/2ox for the ReI complexes provide some supporting for a curved overall relationship with the sum of Lever's electrochemical ligand parameter. The Pickett parametrization for closed-shell complexes is extended now also to 17-electron complexes, i.e. with the 15-electron ReII and FeIII centres in cis-{[ReCl(dppe)2]}+ and trans-{FeBr(depe)2}2+, respectively.

TBAI Catalyzed Electrochemical C-H Bond Activation of 2-arylated-N-methoxyamides for the Synthesis of Phenanthridinones

Synlett ◽  
2021 ◽  
Author(s):  
Kripa Subramanian ◽  
Subhash L. Yedage ◽  
Kashish Sethi ◽  
Bhalchandra M. Bhanage
Keyword(s):  
Electrochemical Method ◽  
Bond Activation ◽  
Supporting Electrolyte ◽  
Bioactive Compound ◽  
Reaction Conditions ◽  
Redox Catalyst ◽  
Synthetic Utility ◽  
One Step ◽  
Constant Potential

An electrochemical method for the synthesis of phenanthridinones via constant potential electrolysis (CPE) mediated by <i>n</i>-Bu<sub>4</sub>NI (TBAI) has been reported. The protocol is metal and oxidant free and proceeds with 100% current efficiency. Here TBAI plays the dual role of the redox catalyst as well as supporting electrolyte. The intramolecular C-H activation proceeds under mild reaction conditions and short reaction time via electrochemically generated amidyl radicals. The reaction has been scaled up to gram level showing its practicability and the synthetic utility and applicability of the protocol has been demonstrated by the direct one-step synthesis of the bioactive compound Phenaglaydon.

Enhanced Electrochemical Oxidation of BH4− on Pt Electrode in Alkaline Electrolyte with the Addition of Thiourea

2010 ◽  
Vol 132 ◽  
pp. 271-278 ◽  
Author(s):  
Dan Mei Yu ◽  
Chang Guo Chen ◽  
Shu Lei ◽  
Xiao Yuan Zhou ◽  
Guo Zhong Cao
Keyword(s):  
Cyclic Voltammetry ◽  
Electrochemical Oxidation ◽  
Electrochemical Impedance ◽  
Alkaline Electrolyte ◽  
Hydroxyl Groups ◽  
Catalytic Hydrolysis ◽  
Direct Oxidation ◽  
Pt Electrode ◽  
Separation Membrane ◽  
And Diffusion

The electrochemical oxidation of sodium borohydride (NaBH4) on Pt electrode in alkaline electrolyte with the addition of thiourea has been studied by means of cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and chronopotentiometry (CP). NaBH4 is readily to react with hydroxyl groups to release hydrogen through either direct oxidation or catalytic hydrolysis. The experimental results demonstrated that the addition of an appropriate amount of thiourea to the alkaline electrolyte resulted in the suppression of catalytic hydrolysis and diffusion of borohydride ions through the separation membrane.

Production of novel carbon nanostructures by electrochemical reduction of polychlorinated organic rings under mild conditions for supercapacitors

2021 ◽  
Author(s):  
Züleyha Kudaş ◽  
Emir Çepni ◽  
Emre Gür ◽  
Duygu Ekinci
Keyword(s):  
Carbon Source ◽  
Electrochemical Reduction ◽  
Electrochemical Method ◽  
Carbon Nanostructures ◽  
Electrochemical Growth ◽  
Mild Conditions ◽  
One Step ◽  
The One ◽  
Carbon Based

Here, new carbon-based nanostructures were prepared by the one-step electrochemical method using hexagonal and pentagonal polychlorinated organic rings as carbon source. The electrochemical growth of carbon nanostructures on substrates was...

scholarly journals Chemical Space Mapping for Multicomponent Gas Mixtures

2021 ◽  
Author(s):  
Airat Kotliar-Shapirov ◽  
Fedor S. Fedorov ◽  
Henni Ouerdane ◽  
Stanislav Evlashin ◽  
Albert G. Nasibulin ◽  
...  
Keyword(s):  
Cyclic Voltammetry ◽  
Data Processing ◽  
Electrochemical Sensors ◽  
Chemical Space ◽  
Chemical Species ◽  
Single Species ◽  
Data Driven ◽  
Multicomponent Gas ◽  
Data Driven Approach ◽  
Cyclic Voltammetry Data

In our manuscript, we present our protocol for data processing to mitigate the effects of interfering analytes on the identification of the chemical species detected by sensors. Considering NO2 and CO2, we designed electrochemical sensors whose response yielded the cyclic voltammetry data that we analyzed to classify single-species components and their mixtures using a data-driven approach to generate a chemical space where their mixtures can be deconvoluted.<br>

scholarly journals Phenol Removal from Wastewaters by Electrochemical Biosensor

2019 ◽  
pp. 24-32
Keyword(s):  
Cyclic Voltammetry ◽  
Electrochemical Impedance Spectroscopy ◽  
Impedance Spectroscopy ◽  
Electrochemical Biosensor ◽  
Electrochemical Impedance ◽  
Experimental Results ◽  
Phenol Oxidation ◽  
Phenol Removal ◽  
Natural Phosphate ◽  
The Matrix

The aim of this work is to introduce bacteria into the matrix of natural phosphate to catalyze the phenol oxidation in the wastewater.This electrode, designated subsequently by bacteria-NP-CPE, Showed stable response and was characterized with voltammeter methods, as cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and DRX. The experimental results revealed that the prepared electrode could be a feasible for degradation of hazardous phenol pollutants in the wastewater.

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