Kaliyamoorthy Selvam and
Meenakshisundaram Swaminathan*
Department of Chemistry, Annamalai University, Annamalainagar, 608 002, India. E-mail: chemres50@gmail.com; Fax: +91 4144 225072
First published on 20th October 2020
Correction for ‘Nano N-TiO2 mediated selective photocatalytic synthesis of quinaldines from nitrobenzenes’ by Kaliyamoorthy Selvam et al., RSC Adv., 2012, 2, 2848–2855, DOI: 10.1039/C2RA01178F.
In the sentence starting on line 5 of paragraph 5 in the introduction:
‘Photocatalytic synthesis of quinolone derivatives from nitrobenzene using TiO2, metal doped TiO2 and others had been reported earlier.1,23–25’
At the end of Section 3.12 with the addition of the following sentence:
‘This catalyst was also found to be effective for the reductive cleavage of azoxybenzenes to amines or 2-phenyl indazoles in methanol.2’
The authors regret that it was not clear in the original article that the bare TiO2 and N-TiO2 characterisation data had been reproduced from their related Journal of Molecular Catalysis A: Chemical, Applied Catalysis A: General and Catalysis Communications papers.1–3 Although the Catalysis Communications article was cited as ref. 25 (ref. 3, in the reference list here) in the original article, it was not made clear that some of the data was reproduced from this article. The appropriate figure captions have been updated to reflect this.
Fig. 2: Diffuse reflectance spectra of (a) bare TiO2, (b) N-TiO2 and (c) TiO2-P25. The bare TiO2 data in Fig. 2a have been reproduced with permission from ref. 1. Copyright 2011 Elsevier. The N-TiO2 data in Fig. 2b have been reproduced with permission from ref. 2. Copyright 2012 Elsevier.
Fig. 3: Photoluminescence spectra of (a) bare TiO2, (b) TiO2-P25 and (c) N-TiO2. The bare TiO2 data in Fig. 3a have been reproduced with permission from ref. 1. Copyright 2011 Elsevier. The N-TiO2 data in Fig. 3c have been reproduced with permission from ref. 2. Copyright 2012 Elsevier.
Fig. 4: HR-TEM analysis: (a and b) images at two different regions of N-TiO2, (c) SAED pattern of N-TiO2, (d) lattice fringes of N-TiO2 and (e) particle size distribution of N-TiO2. Fig. 4 has been entirely reproduced with permission from ref. 2. Copyright 2012 Elsevier.
Fig. 5: X-ray photoelectron spectra of N-TiO2: (a) survey spectrum, (b) Ti 2p peak, (c) O 1s peak, (d) N 1s peak and (e) C peak. Fig. 5 has been entirely reproduced with permission from ref. 2. Copyright 2012 Elsevier.
Fig. 6: (a) N2 adsorption–desorption isotherms of N-TiO2 and (b) its pore size distribution. Fig. 6 has been entirely reproduced with permission from ref. 2. Copyright 2012 Elsevier.
Fig. 8: GC-MS chromatograms at different reaction times for the photocatalytic conversion of nitrobenzene with N-TiO2. Fig. 8 has been entirely reproduced with permission from ref. 3. Copyright 2011 Elsevier.
The authors also wish to remove Fig. 1 from the original article due to similarities between two of the spectra and the raw data no longer being available. This does not affect the conclusions as the presence of nitrogen was confirmed by other techniques.
The authors also wish to clarify the differences between this RSC Advances paper and the Journal of Molecular Catalysis A: Chemical, Applied Catalysis A: General and Catalysis Communications papers.1–3 The Journal of Molecular Catalysis A: Chemical paper discusses the photocatalytic synthesis of quinaldines from nitroarenes by silver loaded TiO2.1 The Applied Catalysis A: General paper reports the reductive cleavage of azoxybenzenes to amines or 2-phenyl indazoles using mesoporous nitrogen doped nano titania.2 The Catalysis Communications paper, ref. 25 in the original article, discusses the synthesis of quinaldines from nitroarenes with gold loaded TiO2 nanoparticles.3 The original RSC Advances paper discusses the catalytic ability of N-TiO2 in the synthesis of quinaldines from nitrobenzenes. In each paper, either a different catalyst was used or a different synthetic reaction was investigated.
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