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ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.

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D. Astruc (Bordeaux), H. Lebel (Montréal), A.-H. Lu (Dalian) | Meet the Board

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Recently Published Articles

  1. You have free access to this content
    Bis–o–Benzosemiquinonato Cobalt(II) and Nickel(II) Complexes with Neutral N-Heterocyclic Carbene Ligand: Synthesis, Structure and Magnetic Properties (pages 2988–2992)

    Dr. Ekaterina V. Bellan, Prof. Andrey I. Poddel'sky, Dr. Natalia A. Protasenko, Dr. Artem S. Bogomyakov, Prof. Georgy K. Fukin, Prof. Vladimir K. Cherkasov and Prof. Gleb A. Abakumov

    Version of Record online: 29 JUL 2016 | DOI: 10.1002/slct.201600506

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    The mixed-ligand N-heterocyclic carbene - bis-o-benzosemiquinonato cobalt(II) and nickel(II) complexes of (3,6-SQ)2M(Me2PhIm) type have been synthesized. Cobalt complex has a square-pyramidal geometry in crystal with NHC ligand in the apical site. Cobalt(II) and nickel(II) in complexes are high-spin and the antiferromagnetic exchange interaction between spins of o-benzosemiquinonato ligands is observed.

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    Different Recognition of TEAD Transcription Factor by the Conserved B-strand:loop:a–helix Motif of the TEAD Binding Site of YAP and VGLL1 (pages 2993–2997)

    Yannick Mesrouze, Dr. Dirk Erdmann, Patrizia Fontana, Marco Meyerhofer, Catherine Zimmermann, Dr. Tobias Schmelzle and Dr. Patrick Chène

    Version of Record online: 28 JUL 2016 | DOI: 10.1002/slct.201600599

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    The coactivators YAP (green) and VGLL1 (blue) bind to the transcription factor TEAD (green) via a conserved α-helix. Despite a high primary sequence homology and a similar binding mode at TEAD surface, these two α-helices have large difference in affinity for TEAD and that they are optimized in a very different manner for binding to TEAD.

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    Counterintuitive Solid-State Syntheses of Indium-Thiolate-Phen Cations as Efficient and Selective Fluorescent Biosensors for HIV-1 ds-DNA and Sudan Ebolavirus RNA Sequences (pages 2979–2987)

    Fu-Ling Li, Shui-Ping Yang, Prof. Wen-Hua Zhang, Quan Liu, Prof. Hong Yu, Prof. Jin-Xiang Chen and Prof. Jian-Ping Lang

    Version of Record online: 28 JUL 2016 | DOI: 10.1002/slct.201600554

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    Indium–thiolate–phenanthroline cations as fluorescent biosensors: In-Tab-Phen (or Dpphen) complexes have been prepared via counterintuitive solid-state reactions at room temperature. These compounds displayed efficient and selective sensing of HIV-1 ds-DNA and Sudan Ebolavirus RNA sequences.

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    Clustered Au on TiO2 Snowman-Like Nanoassemblies for Photocatalytic Applications (pages 2963–2970)

    Vipul Sharma, Suneel Kumar and Dr. Venkata Krishnan

    Version of Record online: 28 JUL 2016 | DOI: 10.1002/slct.201600671

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    In this work, we demonstrate that the concept of having a cluster of noble metal nanoparticles on to a semiconductor oxide provides distinctive advantages in enhancing the photocatalytic performance of hybrid nanoassemblies under both ultraviolet and visible light irradiations.

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    Theoretical Investigation on Mechanism of the PPh3-Catalyzed Isomerization of Allenic Sulfones to 2-Arylsulfonyl 1,3-Dienes: Effects of Additive as the Proton-Shuttle (pages 2971–2978)

    Dr. Binfang Yuan, Prof. Rongxing He, Dr. Wei Shen, Yanyan Xu, Dr. Xiaorui Liu and Prof. Ming Li

    Version of Record online: 28 JUL 2016 | DOI: 10.1002/slct.201600631

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    The PPh3-catalyzed isomerization of allenic sulfones (R) to 2-arylsulfonyl 1,3-dienes (P) reported by Harmata group is employed as a simple model, aiming to illustrate the following issues. a) Exploring the roles of additive in this reaction; b) To explore the regularity of the additive effects as the proton-shuttle. What causes this regularity; c) To predict the acceleration of catalytic amounts EtOH and H2O.