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.
Editorial Board Chairs
D. Astruc (Bordeaux), H. Lebel (Montréal), A.-H. Lu (Dalian) | Meet the Board
Recently Published Articles
- You have free access to this contentBis–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
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.
- You have free access to this contentDifferent 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
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.
- You have free access to this contentCounterintuitive 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
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.
- You have free access to this contentClustered 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
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.
- You have free access to this contentTheoretical 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
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.