[PDF][PDF] Electrochemical and Theoretical Modelled Reduction of β-Diketone Inspired Chalcones

DI Ugwu, J Conradie - 2024 - d-nb.info
The growing interest in synthesizing electrochemically active organic ligands stems from
extensive reports highlighting the applications of redox-active organic molecules. These …

Electrochemical and Theoretical Modelled Reduction of β‐Diketone Inspired Chalcones

D Izuchukwu Ugwu, J Conradie - ChemistrySelect, 2024 - Wiley Online Library
The growing interest in synthesizing electrochemically active organic ligands stems from
extensive reports highlighting the applications of redox‐active organic molecules. These …

Theoretical Study for Isomerization of Some 2-Hydroxychalcone Derivative by Using DFT Calculation

SA Said, OA Shareef, ZW Majed - Egyptian Journal of …, 2021 - ejchem.journals.ekb.eg
In this work we present a study about the molecular structure and electrochemical behavior
of a series of substituted 2´-hydroxychalcones and their conversion to the corresponding …

Electrochemical and density functional theory modeled reduction of enolized 1, 3-diketones

A Kuhn, KG Von Eschwege, J Conradie - Electrochimica acta, 2011 - Elsevier
Cathodic peak potentials (E pc) of ten enolized 1, 3-substituted 1, 3-diketones, R 1 COCHC
(OH) R 2 derivatives containing electron withdrawing and/or electron donating groups, were …

Electrochemical and DFT study of the reduction of substituted phenanthrolines

H Ferreira, MM Conradie, KG von Eschwege… - Polyhedron, 2017 - Elsevier
The irreversible electrochemical reduction data of a series of free uncoordinated differently
substituted phenanthrolines is presented. Electron withdrawing chloride substituents in the …

Theoretical and Experimental Studies on the Positional Impact of Hydroxyl Groups on the Electrochemical Oxidative Behaviour of Di-Hydroxybenzenes

N CHANDRAKANTH, K Jathi - Available at SSRN 4740143 - papers.ssrn.com
The impact of the position of the electron-donating hydroxyl groups on the oxidative
behaviour of dihydroxybenzenes were determined by using cyclic voltammetry (CV) …

[HTML][HTML] Electrochemical behaviour of 2-hydroxybenzophenones and related molecules

E Chiyindiko, EHG Langner, J Conradie - Results in Chemistry, 2022 - Elsevier
An electrochemical study, using cyclic voltammetry of 2-hydroxybenzophenone and related
molecules, containing various electron withdrawing and/or electron donating groups, is …

Electron affinities, solvation energies and redox potentials of some chalcones: substituentseffect and correlation with semi-empirical MO energies

A Rahman, R Qureshi, M Kiran… - Turkish Journal of …, 2007 - journals.tubitak.gov.tr
Experimental and theoretical investigations were carried out on 2 sets of chalcones. Set 1
has an OH group on ring A and Set 2 does not, and both have different substituents on ring …

Substituent effects on the redox potentials of dihydroxybenzenes: theoretical and experimental study

T Liu, MM Liu, XW Zheng, CY Du, XY Cui, L Wang… - Tetrahedron, 2014 - Elsevier
The redox reactions of p-hydroquinone and pyrocatechol undergo a two-proton-two-electron
process in aqueous solution. We calculated their redox potentials at the B3LYP/6-311+ G (d …

Reduction potential of benzophenones, hydroxyphenones and bis (2-hydroxyphenone) copper molecules

J Conradie - Electrochimica Acta, 2023 - Elsevier
In this study the redox behaviour of three different series of molecules are discussed and
compared. The first series consist of 24 differently substituted benzophenones (BPs). The …