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Cover image for Vol. 7 Issue 5

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

Associated Title(s): Advanced Synthesis & Catalysis, Angewandte Chemie International Edition, Chemistry - A European Journal, ChemBioChem, ChemElectroChem, ChemPhysChem, ChemSusChem

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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

  1. Promoting Visible-Light Photocatalysis with Palladium Species as Cocatalyst

    Xiuzhen Li, Nan Zhang and Prof. Yi-Jun Xu

    Article first published online: 6 MAR 2015 | DOI: 10.1002/cctc.201500009

    Thumbnail image of graphical abstract

    Duality is part of life: Ternary In2S3– (reduced graphene oxide–palladium) composites show enhanced visible-light photoactivity with the introduction of palladium nanoparticles, which act as dual cocatalyst with reduced graphene oxide.

  2. Magnetically Recoverable Catalysts with Dendritic Ligands for Enhanced Catalysis and Easy Separation

    Dr. Lyudmila M. Bronstein

    Article first published online: 6 MAR 2015 | DOI: 10.1002/cctc.201500007

    Thumbnail image of graphical abstract

    A smart design: Magnetically recoverable catalysts that use dendritic ligands to remain either directly on the surface of iron oxide nanoparticles, or on a silica intermediary layer, allow the fabrication of catalysts with significantly enhanced catalytic properties for a wide range of reactions.

  3. Direct Synthesis of Hydrogen Peroxide over Au-Pd Catalyst—The Effect of Co-Solvent Addition

    Violeta Paunovic, Dr. Vitaly V. Ordomsky, Dr. Vitaly L. Sushkevich, Prof. Dr. Jaap C. Schouten and Dr. T. Alexander Nijhuis

    Article first published online: 2 MAR 2015 | DOI: 10.1002/cctc.201500050

    Thumbnail image of graphical abstract

    Solvent provides the solution! The direct synthesis represents a green alternative, environmentally benign, process for the production of hydrogen peroxide. The liquid phase used in the direct synthesis has a role to collect hydrogen peroxide from the catalyst surface preventing its decomposition. Here we show that the choice of solvent used in the liquid phase has a tremendous effect not only on conversion, but on selectivity towards the desired product.

  4. Tuneable Hydrogenation of Nitriles into Imines or Amines with a Ruthenium Pincer Complex under Mild Conditions

    Jong-Hoo Choi and Dr. Martin H. G. Prechtl

    Article first published online: 2 MAR 2015 | DOI: 10.1002/cctc.201403047

    Thumbnail image of graphical abstract

    Synthetic double punch: The selective hydrogenation of nitriles into amines and imines is described. The selectivity towards amines or imines can be controlled by using a ruthenium pincer complex. The reactions are conducted at low temperature and low pressure without any additives at low catalytic loadings of 0.5–1 mol %, which results in quantitative conversions and high selectivity.

  5. The Multiple Roles of Imidazolium Ionic Liquids in Transition-Metal Catalysis: The Palladium-Catalyzed Telomerization of 1,3-Butadiene with Acetic Acid

    MSc. João M. Balbino, Dr. Daniel Peral, Prof. J. Carles Bayón and Prof. Jairton Dupont

    Article first published online: 2 MAR 2015 | DOI: 10.1002/cctc.201402943

    Thumbnail image of graphical abstract

    Completing the puzzle: A Pd catalyst with the Dan2phos ligand, a new trifluoromethylated and sulfonated phosphine, and MeOImAcO, an ionic liquid with an acetate anion, is the right combination for the telomerization of 1,3-butadiene with acetic acid.

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