Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Editor: Michael Rowan; Editorial Board Chairs: Uwe Bornscheuer, Luis A. Oro, Bert Weckhuysen
Impact Factor: 5.044
ISI Journal Citation Reports © Ranking: 2013: 26/136 (Chemistry Physical)
Online ISSN: 1867-3899
February 01, 2014
New Online Manuscript Submission System
We are pleased to announce that after over ten years, manuscriptXpress was replaced by a new Manuscript handling system, EditorialManager from ARIES, on February 1.
The links to the new journal sites are available at: chemistryviews.org/submission.
Articles that have been submitted to manuscriptXpress will be processed from there.
Thank you for your patience and we look forward to receiving your next excellent manuscript.
Recently Published Articles
- Exploring the Reactivity of Nickel Pincer Complexes in the Decomposition of Formic Acid to CO2/H2 and the Hydrogenation of NaHCO3 to HCOONa
Dr. Stephan Enthaler, Dr. Andreas Brück, Anja Kammer, Dr. Henrik Junge, Dr. Elisabeth Irran and Dr. Samet Gülak
Article first published online: 19 OCT 2014 | DOI: 10.1002/cctc.201402716
A nickel for your hydrogen economy: The catalytic abilities of nickel complexes modified by a PCP pincer ligand in the decomposition of formic acid to produce dihydrogen and carbon dioxide have been studied.
- Photocatalytic Hydrogen Evolution from Silica-Templated Polymeric Graphitic Carbon Nitride–Is the Surface Area Important?
Dr. Xiaobo Li, Prof. Anthony F. Masters and Prof. Thomas Maschmeyer
Article first published online: 19 OCT 2014 | DOI: 10.1002/cctc.201402567
More H2 through silica templating: Mesoporous-silica-templated, low-surface-area, polymeric graphitic carbon nitride (SBA–g-C3N4) exhibits a greatly improved photocatalytic hydrogen evolution rate on a per-surface area basis compared to that of conventional bulk graphitic carbon nitrides. The intrinsically high surface activity of SBA–g-C3N4 was confirmed for both homo- (cobaloxime) and heterogeneous (Pt) co-catalyst systems (TEOA=triethanolamine).
- Eco-Friendly Catalytic Systems Based on Carbon-Supported Magnesium Oxide Materials for the Friedländer Condensation
Marina Godino-Ojer, Prof. Antonio J. López-Peinado, Prof. Rosa M. Martín-Aranda, Dr. Jacek Przepiórski, Dr. Elena Pérez-Mayoral and Dr. Elena Soriano
Article first published online: 19 OCT 2014 | DOI: 10.1002/cctc.201402602
Oxide, outside: MgO supported on carbon is able to catalyze the synthesis of interesting N-containing heterocyclic compounds efficiently under mild conditions. MgO on the carbon surface is responsible for the catalytic behavior. These carbon materials are environmentally friendly catalysts for the Friedländer reaction.
- Highly Efficient and Magnetically Recoverable Niobium Nanocatalyst for the Multicomponent Biginelli Reaction
Carolina G. S. Lima, Dr. Sandrina Silva, Ricardo H. Gonçalves, Prof. Dr. Edson R. Leite, Prof. Dr. Ricardo S. Schwab, Prof. Dr. Arlene G. Corrêa and Prof. Dr. Márcio W. Paixão
Article first published online: 16 OCT 2014 | DOI: 10.1002/cctc.201402689
Magnetic personality: A new magnetically recoverable nanocatalyst, Fe3O4@Nb2O5, is prepared and fully characterized. Its catalytic activity is evaluated by using the one-pot, three-component Biginelli reaction, with the aim to synthesize 1,4-dihydropyrimidinones. The new nanocatalyst proves to be highly efficient in synthesizing a wide range of Biginelli products and has the advantage of a remarkably low catalyst loading (0.1 mol %) and high reusability.
- Sulfonated Core-Shell Magnetic Nanoparticle (Fe3O4@SiO2@PrSO3H) as a Highly Active and Durable Protonic Acid Catalyst; Synthesis of Coumarin Derivatives through Pechmann Reaction
Dr. Farhad Kabiri Esfahani, Dr. Daryoush Zareyee and Reza Yousefi
Article first published online: 16 OCT 2014 | DOI: 10.1002/cctc.201402547
Green earth and blue sky: Herein, we wish to disclose a simple bench top procedure for the synthesis of sulfonated core-shell magnetic nanoparticles (SMNPs) (Fe3O4@SiO2@PrSO3H) and discuss its performance as a very strong solid acid in the Pechmann condensation reaction.