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Cover image for Vol. 7 Issue 14

Editor: Michael Rowan; Editorial Board Chairs: Uwe Bornscheuer, Luis A. Oro, Bert Weckhuysen

Impact Factor: 4.556

ISI Journal Citation Reports © Ranking: 2014: 31/139 (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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March 24, 2015

New Online Manuscript Submission System

We are pleased to announce that after over ten years, manuscriptXpress has been replaced by a new manuscript handling system, EditorialManager from ARIES.

The links to the new journal sites are available at: chemistryviews.org/submission.

Thank you for your patience and we look forward to receiving your next excellent manuscript.

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Recently Published Articles

  1. Performance of Recombinant-Whole-Cell-Catalyzed Reductions in Deep-Eutectic-Solvent–Aqueous-Media Mixtures

    Christoph R. Müller, Iván Lavandera, Vicente Gotor-Fernández and Pablo Domínguez de María

    Article first published online: 31 JUL 2015 | DOI: 10.1002/cctc.201500428

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    DESirable biocatalysis: Several enzymes, like Ralstonia sp. alcohol dehydrognase (RasADH) overexpressed in Escherichia coli, remain active for the stereoselective reduction of ketones in various deep-eutectic-solvents (DES)–buffer solutions. Furthermore, the ee values obtained for a broad range of aromatic substrates increase significantly if the DES mixture is added.

  2. An Empirical Study of Phosphine Ligands for the Methoxycarbonylation of Medium-Chain Alkenes

    Prof. Cedric Holzapfel and Dr. Tyler Bredenkamp

    Article first published online: 31 JUL 2015 | DOI: 10.1002/cctc.201500464

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    The cat’s out of the bag: A comparative study of various phosphine ligands is undertaken to discern the necessary requirements for a suitable catalyst for the methoxycarbonylation of higher aliphatics. Our findings demonstrate that a number of ligand structural motifs can facilitate the reaction effectually and that the most promising ligands bear one bulky electron-rich P atom and one bulky electron-poor P atom, demonstrating a catopdative-like effect.

  3. Highly Active and Stable Palladium Nanoparticles Encapsulated in a Mesoporous Silica Yolk–Shell Nanoreactor for Suzuki–Miyaura Reactions

    Fang Wei, Dr. Changyan Cao, Yongbin Sun, Shuliang Yang, Peipei Huang and Prof. Dr. Weiguo Song

    Article first published online: 29 JUL 2015 | DOI: 10.1002/cctc.201500600

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    Core catalysis: A yolk–shell nanoreactor with nitrogen-doped carbon spheres as the yolk and mesoporous silica (mSiO2) as the shell, together with Pd nanoparticles uniformly encapsulated in the void space, showed excellent catalytic activity and stability in the Suzuki–Miyaura reaction. CTAB=Hexadecyl trimethyl ammonium bromide, PDA=Polydopamine, TEOS=Tetraethyl orthosilicate.

  4. Enhancement of Photoelectrochemical Performance in Water Oxidation over Bismuth Vanadate Photoanodes by Incorporation with Reduced Graphene Oxide

    Yingfei Hu, Yao Su, Huiting Huang, Qinfeng Qian, Zhongjie Guan, Dr. Jianyong Feng, Prof. Zhaosheng Li and Prof. Zhigang Zou

    Article first published online: 29 JUL 2015 | DOI: 10.1002/cctc.201500485

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    Change the channel: Reduced graphene oxide (RGO) sheets with excellent electronic conductivity are introduced to bismuth vanadate photoanode films to provide an effective channel for electron transport. The proposed mechanism of charge transport for the reduced graphene oxide–bismuth vanadate photoelectrode under irradiation is depicted. FTO=Fluorine-doped tin oxide.

  5. Highly Selective Hydrodecarbonylation of Oleic Acid into n-Heptadecane over a Supported Nickel/Zinc Oxide–Alumina Catalyst

    Dr. Guangci Li, Feng Zhang, Dr. Lei Chen, Chuanhui Zhang, Dr. He Huang and Prof. Dr. Xuebing Li

    Article first published online: 28 JUL 2015 | DOI: 10.1002/cctc.201500418

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    Basic rules! A suitable amount of basicity on the support is favorable for the conversion of oleic acid into n-alkanes mainly through hydrodecarbonylation with relatively low hydrogen consumption.

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