© WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
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
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We are pleased to announce that after over ten years, manuscriptXpress has been replaced by a new manuscript handling system, EditorialManager from ARIES.
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Thank you for your patience and we look forward to receiving your next excellent manuscript.
Recently Published Articles
- N-Heterocyclic Carbene–Pd Polymers as Reusable Precatalysts for Cyanation and Ullmann Homocoupling of Aryl Halides: The Role of Solvent in Product Distribution
Prof. Dr. Babak Karimi, Dr. Majid Vafaeezadeh and Dr. Pari Fadavi Akhavan
Article first published online: 1 JUL 2015 | DOI: 10.1002/cctc.201500383
Switch the solvent: An NHC-Pd polymer with an N-dodecyl group was found to be a highly efficient and recyclable catalyst for cyanation and the Ullmann homocoupling reaction. The employed solvent exhibited a critical influence in the product distribution.
- Does the Surface Structure of Oxide Affect the Strong Metal–Support Interaction with Platinum? Platinum on Fe3O4(0 0 1) versus Fe3O4(1 1 1)
Ke Zhang, Dr. Shamil Shaikhutdinov and Prof. Dr. Hans-Joachim Freund
Article first published online: 1 JUL 2015 | DOI: 10.1002/cctc.201500328
The effect remains the same: Platinum deposited on the (√2×√2)R45°-reconstructed surface of Fe3O4(0 0 1) thin films exhibits a strong metal–support interaction that results in cuboid Pt nanoparticles, with edges oriented along the crystallographic directions of the Fe3O4(0 0 1) surface, encapsulated by an FeO(1 1 1) single layer, which is the same as observed previously for hemispherical Pt particles on a Fe3O4(1 1 1) support.
- The Pyridyl Functional Groups Guide the Formation of Pd Nanoparticles Inside A Porous Poly(4-Vinyl-Pyridine)
Dr. Elena Groppo, Dr. Giovanni Agostini, Dr. Elisa Borfecchia, Andrea Lazzarini, Dr. Wei Liu, Prof. Dr. Carlo Lamberti, Dr. Francesco Giannici, Dr. Giuseppe Portale and Dr. Alessandro Longo
Article first published online: 1 JUL 2015 | DOI: 10.1002/cctc.201500211
N attraction: The reactivity of palladium acetate inside a poly(4-vinylpyridine-co-divinylbenzene) polymer is strongly influenced by the establishment of strong interaction between the palladium precursor and the pyridyl functional group in the polymer, as determined by IR spectroscopy and simultaneous X-ray absorption techniques in the presence of H2 or CO as a function of temperature.
- Suzuki–Miyaura Diversification of Amino Acids and Dipeptides in Aqueous Media
Tom Willemse, Karolien Van Imp, Dr. Rebecca J. M. Goss, Prof. Dr. Herman W. T. Van Vlijmen, Dr. Wim Schepens, Prof. Dr. Bert U. W. Maes and Prof. Dr. Steven Ballet
Article first published online: 29 JUN 2015 | DOI: 10.1002/cctc.201500190
Get down and derivatise! The palladium-catalysed Suzuki–Miyaura derivatisation of (un)protected Phe or Trp, and peptide substrates containing halogenated Phe or Trp, is performed via use of various water-compatible catalytic systems. By mimicking the natural aqueous environment of peptides, halogenated moieties are transformed to a variety of (hetero)aryl and vinyl subtituents.
- A Viable Hydrogen Storage and Release System Based on Cesium Formate and Bicarbonate Salts: Mechanistic Insights into the Hydrogen Release Step
Katerina Sordakis, Andrew F. Dalebrook and Prof. Dr. Gábor Laurenczy
Article first published online: 26 JUN 2015 | DOI: 10.1002/cctc.201500359
Cesium cycling: In the presence of a ruthenium catalytic precursor and a stabilizing phosphine ligand, cesium formate and bicarbonate in aqueous solution perform as a stable hydrogen storage–release couple. An intermediate pentacoordinated 16-electron ruthenium hydride complex is crucial in the promotion of the formate dehydrogenation.