ChemCatChem

Cover image for Vol. 9 Issue 10

Editor: Michael Rowan; Editorial Board Chairs: Uwe Bornscheuer, Hermenegildo García, A. Stephen K. Hashmi

Impact Factor: 4.724

ISI Journal Citation Reports © Ranking: 2015: 29/144 (Chemistry Physical)

Online ISSN: 1867-3899

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

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August 10, 2016

ChemCatChem Board Members receive Catalysis Awards

Two ChemCatChem board members have received prestigious awards at the 16th International Congress on Catalysis (ICC) in Beijing, P.R. China. Dr. David Farrusseng, IRCE Lyon, CNRS, (France) has received the International Catalysis Award 2016. He presented a Plenary Lecture entitled "Catalysis Inside a Box" at the ICC.

Prof. Paolo Fornasiero, University of Trieste (Italy) has received the Heinz Heinemann Award 2016. He presented a Plenary Lecture entitled "Hybrid Nanocatalysts for Energy Related Applications" at the ICC.

We congratulate both of them and thank them for their support!

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    Jinhuo Dai, Antonio Patti, Lionel Longé, Gil Garnier and Kei Saito

    Accepted manuscript online: 25 MAY 2017 06:20AM EST | DOI: 10.1002/cctc.201700632

  2. The Role of Gas in Determining Image Quality and Resolution During In Situ Scanning Transmission Electron Microscopy Experiments

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    Accepted manuscript online: 24 MAY 2017 09:20PM EST | DOI: 10.1002/cctc.201700474

  3. A Highly Active PBP–Iridium Catalyst for the Dehydrogenation of Dimethylamine–Borane: Catalytic Performance and Mechanism

    Dr. Enrique Huang Kwan, Hayato Ogawa and Prof. Dr. Makoto Yamashita

    Version of Record online: 24 MAY 2017 | DOI: 10.1002/cctc.201700384

    Thumbnail image of graphical abstract

    Stuck like PB: A newly synthesized boron-containing pincer ligand with an aliphatic backbone is treated with [Ir(coe)2Cl]2 (coe=cyclooctene) to result in (P-B-P)Ir(H)Cl. A catalyst system comprising this Ir complex and KOtBu shows excellent performance in releasing 1 equivalent of H2 from the N,N-dimethylamine–borane complex at a low catalyst loading (0.05 mol %) with an initial turnover frequency (TOF) of approximately 3400 h−1.

  4. Palladium Nanoparticles Encaged in a Nitrogen-Rich Porous Organic Polymer: Constructing a Promising Robust Nanoarchitecture for Catalytic Biofuel Upgrading

    Ramana Singuru, Karnekanti Dhanalaxmi, Subhash Chandra Shit, Prof. Dr. Benjaram Mahipal Reddy and Prof. Dr. John Mondal

    Version of Record online: 23 MAY 2017 | DOI: 10.1002/cctc.201700186

    Thumbnail image of graphical abstract

    POP goes the nanoparticle: Robust nanoarchitectures based on surfactant-free ultrafine Pd nanoparticles (NPs) were developed by using the incipient wetness impregnation method with subsequent reduction of the PdII species encaged in the 1,3,5-triazine-functionalized nitrogen-rich porous organic polymer (POP) by NaBH4, HCHO, and H2. Strong metal–support interactions, the nanoconfinement effect of POP, and the homogeneous distribution of Pd NPs have been investigated along with the catalysts’ effectiveness in the hydrodeoxygenation of vanillin, a typical compound of lignin-derived bio-oil.

  5. Tandem Diels–Alder Reaction of Dimethylfuran and Ethylene and Dehydration to para-Xylene Catalyzed by Zeotypic Lewis Acids

    Ryan E. Patet, Prof. Wei Fan, Prof. Dionisios G. Vlachos and Dr. Stavros Caratzoulas

    Version of Record online: 23 MAY 2017 | DOI: 10.1002/cctc.201601584

    Thumbnail image of graphical abstract

    What catalyzes the Diels–Alder reaction? Although Lewis acids can catalyze the dehydration of the Diels–Alder (DA) cycloadduct, it is unclear whether these same catalysts can catalyze the DA step. Thus, electronic structure calculations and microkinetic modelling have been employed to investigate the DA aromatization of 2,5-dimethylfuran and ethylene to p-xylene over the Lewis-acidic zeotypes Sn-, Zr-, and Ti-BEA. The results show that there is only minor catalysis of the DA reaction, solely attributable to confinement phenomena varying with the translational freedom allowed to the species inside the zeolite.

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