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Correction: Water oxidation by a copper(II) complex: new findings, questions, challenges and a new hypothesis

Mohammad Mahdi Najafpour *abc, Somayeh Mehrabani a, Younes Mousazade a and Małgorzata Hołyńska d
aDepartment of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan, 45137-66731, Iran. E-mail: mmnajafpour@iasbs.ac.ir; Tel: +9824 3315 3201
bCenter of Climate Change and Global Warming, Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan, 45137-66731, Iran
cResearch Center for Basic Sciences & Modern Technologies (RBST), Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan 45137-66731, Iran
dFachbereich Chemie and Wissenschaftliches Zentrum für Materialwissenschaften (WZMW), Philipps-Universität Marburg, Hans-Meerwein-Straße, D-35032 Marburg, Germany

Received 8th August 2018 , Accepted 8th August 2018

First published on 16th August 2018


Abstract

Correction for ‘Water oxidation by a copper(II) complex: new findings, questions, challenges and a new hypothesis’ by Mohammad Mahdi Najafpour et al., Dalton Trans., 2018, 47, 9021–9029.


The authors would like to correct part b of Fig. 1, which, in the published manuscript, is the same as part a. The correct Fig. 1 is shown below:
image file: c8dt90139b-f1.tif
Fig. 1 CVs (scan rate: 50.0 mV s−1; a, b) for 1 (red), 2 (blue), 3 (olive), 4 (gray), copper(II) salt (pink), and bare FTO electrode (black as a reference) in the buffer solution. The continuous CV for 2 at (−1.2)–(−0.5) V (c). Amperometry for 1 (red), 2 (blue), 3 (olive), 4 (gray), copper(II) salt (pink) and bare FTO electrode (black as a reference) in the buffer solution (d). The orange arrows indicate the peak attributed to uncomplexed Cu(II) species. The conditions: in the phosphate buffer solution (0.25 M, pH = 11.0) at room temperature. The electrochemical studies were carried out with a conventional three-electrode setup, in which FTO, Ag/AgCl/KClsat and platinum foil served as working, reference and auxiliary electrodes, respectively. The concentrations of copper(II) compounds were 0.25 mM.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


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