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
- Improving Oxygen Electrochemistry through Nanoscopic Confinement
Andrew D. Doyle, Joseph H. Montoya and Dr. Aleksandra Vojvodic
Article first published online: 30 JAN 2015 | DOI: 10.1002/cctc.201402864
Nanostructuring catalysts: Density functional theory calculations show that well-defined reaction geometries substantially improve the activity of RuO2 catalysts for electrochemical oxygen evolution. Enhanced efficiency is primarily due to hydrogen bonding, which breaks the previously limiting energetic scaling relationships of the reaction intermediates.
- Design of a Hierarchical Meso/Macroporous Zeolite-Supported Cobalt Catalyst for the Enhanced Direct Synthesis of Isoparaffins from Syngas
Qihang Lin, Guohui Yang, Qingjun Chen, Ronggang Fan, Yoshiharu Yoneyama, Prof. Huilin Wan and Prof. Noritatsu Tsubaki
Article first published online: 30 JAN 2015 | DOI: 10.1002/cctc.201402929
I’ve seen the zeolite! A hierarchical meso/macroporous zeolite is developed by a steam-assisted crystallization method using alumina-modified meso/macroporous silica as the precursor. After the loading of Co, the as-synthesized catalyst exhibits excellent performance for the direct synthesis of isoparaffins because of the strong acidic sites of the β-zeolite and its unique hierarchical meso/macroporous structure.
- Imidazole Derivatives as Accelerators for Ruthenium-Catalyzed Hydroesterification and Hydrocarbamoylation of Alkenes: Extensive Ligand Screening and Mechanistic Study
Dr. Hideyuki Konishi, Takashi Muto, Dr. Tsuyoshi Ueda, Yayoi Yamada, Dr. Miyuki Yamaguchi and Prof. Dr. Kei Manabe
Article first published online: 30 JAN 2015 | DOI: 10.1002/cctc.201402986
Effective imidazole assistant: [Ru3(CO)12]-catalyzed hydroesterification of alkenes by using formates is drastically accelerated by imidazole derivatives and exhibits a broad substrate scope for both alkenes and formates. The Ru– imidazole complex also catalyzes the intramolecular hydrocarbamoylation of alkenes.
- Nanostructured Encapsulated Catalysts for Combination of Fischer–Tropsch Synthesis and Hydroprocessing
Nadine Kruse, Albert G. Machoke, Prof. Dr. Wilhelm Schwieger and Prof. Dr. Robert Güttel
Article first published online: 30 JAN 2015 | DOI: 10.1002/cctc.201403004
Under control: Controlling the selectivity of Fischer–Tropsch (FT) synthesis in a single reaction step is a major challenge in heterogeneous catalysis. An innovative synthetic approach that allows the bottom-up construction of nanostructured bifunctional catalysts in a step-wise manner is described. The resulting material, which exhibits cobalt nanoparticles encapsulated inside a zeolite matrix, is proven to shift the FT selectivity from waxy to liquid products.
- Cp*CoIII-Catalyzed CH Activation of (Hetero)arenes: Expanding the Scope of Base-Metal-Catalyzed CH Functionalizations
Prof. Naohiko Yoshikai
Article first published online: 30 JAN 2015 | DOI: 10.1002/cctc.201403017
Directed activation: Cationic Cp*CoIII (Cp*=1,2,3,4,5-pentamethylcyclopentadienyl) complexes, either well-defined or in situ-generated, promote catalytic functionalization of arene CH bonds with a variety of electrophilic reaction partners by directed CH activation. These complexes not only emulate known reaction patterns of Cp*RhIII analogues, but also exhibit remarkable catalytic activity or unique reactivity. DG=Directing group.