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
- Multicomponent Approach to Silica-Grafted Peptide Catalysts: A 3 D Continuous-Flow Organocatalytic System with On-line Monitoring of Conversion and Stereo- selectivity
Gabriel S. Scatena, Alexander F. de la Torre, Prof. Dr. Quezia B. Cass, Prof. Dr. Daniel G. Rivera and Prof. Dr. Márcio W. Paixão
Article first published online: 22 SEP 2014 | DOI: 10.1002/cctc.201402501
Fully automated: A 3 D continuous-flow organocatalytic system is designed with the integration of the microreactor and multidimensional chromatography technologies. This enamine catalysis platform enables the production of chiral γ-nitroaldehydes with on-line monitoring of the reaction parameters. Boc=tert-Butoxycarbonyl, dr=diastereomeric ratio.
- Niobium Peroxide-Catalyzed Selective Epoxidation of Allylic Alcohols
Chen Chen, Xiuge Zhao, Jizhong Chen, Li Hua, Ran Zhang, Li Guo, Baoning Song, Huimei Gan and Prof. Dr. Zhenshan Hou
Article first published online: 22 SEP 2014 | DOI: 10.1002/cctc.201402545
Making it look easy is difficult: Niobium peroxides modified with surfactants are prepared and used for catalyzing the epoxidation of allylic alcohols with hydrogen peroxide in the absence of any other solvent. The modified amphiphilic catalysts allow easier accessibility to hydrophobic substrates and thus demonstrate high reaction rate and excellent recyclability for the epoxidation under mild conditions.
- Heterobimetallic Metal–Organic Framework as a Precursor to Prepare a Nickel/Nanoporous Carbon Composite Catalyst for 4-Nitrophenol Reduction
Dr. Ying Yang, Dr. Ying Zhang, Dr. Cheng Jun Sun, Xinsong Li, Wen Zhang, Xiaohui Ma, Dr. Yang Ren and Prof. Dr. Xin Zhang
Article first published online: 18 SEP 2014 | DOI: 10.1002/cctc.201402607
A tailored fit: Thermal conversion of heterobimetallic zinc–nickel–terephthalate frameworks yields mesoporous nickel/mesoporous carbon (MC) composite catalysts for the reduction of 4-nitrophenol. Tailoring the Ni/Zn ratio in the precursor compounds (Zn1−xNixMOF, x≈0–1, MOF=metal–organic framework) creates densely populated and smaller Ni nanocrystals (Ni NCs) while maintaining sufficient porosity and surface area.
- Formic Acid Dehydrogenation Catalysed by Tris(TPPTS) Ruthenium Species: Mechanism of the Initial “Fast” Cycle
Arnaud Thevenon, Ewan Frost-Pennington, Dr. Gan Weijia, Dr. Andrew F. Dalebrook and Prof. Gábor Laurenczy
Article first published online: 18 SEP 2014 | DOI: 10.1002/cctc.201402410
Two phosphines or three? Ruthenium m-triphenylphosphinetrisulfonate (TPPTS) complexes are highly active for aqueous phase formic acid dehydrogenation. Using a series of NMR experiments, several active intermediates that each bind three TPPTS units have been identified. The system activity decreases with the loss of one phosphine ligand upon progression to the slower catalytic cycle.
- Self-Regenerative Property of Nanocrystalline Ce0.89M0.11O2−y (M=Pd, Rh) Mixed Oxides
Dr. Michalina Kurnatowska, Dr. Manfred E. Schuster, Dr. Wlodzimierz Mista and Prof. Leszek Kepinski
Article first published online: 18 SEP 2014 | DOI: 10.1002/cctc.201402480
Born to rise again: Self-regenerative properties of nanocrystalline Ce0.89M0.11O2−y (M=noble metal, e.g., Pd and Rh) mixed oxides are investigated by applying the reduction–oxidation treatment. The redox properties of Ce0.89Rh0.11O2−y are completely reversible after the reduction–oxidation treatment, whereas those of Ce0.89Pd0.11O2−y are only partially reversible.