© WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Editor-in-Chief: Guido Kemeling; Editorial Board Chairs: Matthias Beller, Gabriele Centi, Licheng Sun
Impact Factor: 7.657
ISI Journal Citation Reports © Ranking: 2014: 18/157 (Chemistry Multidisciplinary)
Online ISSN: 1864-564X
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.
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Recently Published Articles
- Levulinic Acid Biorefineries: New Challenges for Efficient Utilization of Biomass
Filoklis D. Pileidis and Prof. Maria-Magdalena Titirici
Article first published online: 5 FEB 2016 | DOI: 10.1002/cssc.201501405
Refined and ready: Lignocellulosic biomass upgrade through the use of levulinic acid offers a wide array of products with a variety of applications ranging from fuel additives to biobased chemicals, green solvents, biopolymers, and biofertilizers.
- The Role of MgCl2 as a Lewis Base in ROMgCl–MgCl2 Electrolytes for Magnesium-Ion Batteries
Dr. Baofei Pan, Dr. Jinhua Huang, Meinan He, Dr. Scott M. Brombosz, Dr. John T. Vaughey, Dr. Lu Zhang, Dr. Anthony K. Burrell, Dr. Zhengcheng Zhang and Dr. Chen Liao
Article first published online: 4 FEB 2016 | DOI: 10.1002/cssc.201501557
Switching roles: A series of strong Lewis-acid-free alkoxide/siloxide-based Mg electrolytes are developed with remarkable oxidative stability up to 3.5 V (vs. Mg/Mg2+). Despite the perception of ROMgCl (R=alkyl, silyl) as a strong base, ROMgCl acts like a Lewis acid, whereas the role of MgCl2 is unambiguously demonstrated as a Lewis base through the identification of the key intermediate using single-crystal X-ray crystallography.
- Evaluation of Metal-Organic Frameworks and Porous Polymer Networks for CO2-Capture Applications
Wolfgang M. Verdegaal, Kecheng Wang, Dr. Julian P. Sculley, Prof. Dr. Mario Wriedt and Prof. Dr. Hong-Cai Zhou
Article first published online: 3 FEB 2016 | DOI: 10.1002/cssc.201501464
Capture-all: The physical properties of a diverse set of porous materials are experimentally obtained, fed into a carbon-capture model, and evaluated according to the working capacity of CO2 separated from flue gas per energy by comparing seven different carbon-capture scenarios. This method provides a tool for researchers to make more meaningful comparisons of their data to literature results.
- Hybrid Amine-Functionalized Graphene Oxide as a Robust Bifunctional Catalyst for Atmospheric Pressure Fixation of Carbon Dioxide using Cyclic Carbonates
Vitthal B. Saptal, Prof. Takehiko Sasaki, Kei Harada, Dr. Daisuke Nishio-Hamane and Prof. Bhalchandra M. Bhanage
Article first published online: 3 FEB 2016 | DOI: 10.1002/cssc.201501438
Re-cyclo-addition: Amine-functionalized graphene oxide (AP-GO) is presented as an environmentally-benign carbocatalyst for the conversion of epoxides to cyclic carbonates using CO2. The synthesis and characterization of this catalyst is described, along with thorough optimization of the reaction conditions for the carbocatalyzed cycloaddition reaction under mild temperatures and pressures. AP-GO is proved to be a highly active catalyst for the synthesis of cyclic carbonates and can be recycled up to seven times without losing its catalytic activity.
- Metal-free Nanoporous Carbon as a Catalyst for Electrochemical Reduction of CO2 to CO and CH4
Wanlu Li, Dr. Mykola Seredych, Prof. Enrique Rodríguez-Castellón and Prof. Teresa J. Bandosz
Article first published online: 2 FEB 2016 | DOI: 10.1002/cssc.201501575
Double doped! S,N-doped polymer-derived carbons are studied as electrocatalysts for the reduction of CO2 to CO and CH4. Higher Faradaic efficiencies are obtained on dual S,N-doped carbon than on its S-doped counterpart. The presence of positively charged sites and the incorporation of functional groups promotes the electrochemical reduction of CO2 and the ultra-micropores enhance the reduction of CO2 to CH4.