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ChemCatChem

Cover image for Vol. 2 Issue 8

Edited by: Peter Gölitz, Deputy Editor: David Smith

Online ISSN: 1867-3899

Associated Title(s): ChemBioChem, ChemMedChem, ChemPhysChem, ChemSusChem

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aldehydes · arenes · asymmetric catalysis · asymmetric synthesis · biocatalysis · C-C coupling · C-H activation · carbon · copper · enantioselectivity · gold · heterogeneous catalysis · homogeneous catalysis · hydrogenation · IR spectroscopy · mesoporous materials · nanoparticles · nitrogen oxides · organocatalysis · oxidation · palladium · platinum · reaction mechanisms · reduction · rhodium · ruthenium · silver · supported catalysts · transition metals · zeolites

Recently Published Articles

  1. Creating Cellulose-Binding Domain Fusions of the Coenzyme A Biosynthetic Enzymes to Enable Reactor-Based Biotransformations

    Ilse Rootman, Marianne de Villiers, Leisl A. Brand and Erick Strauss

    Article first published online: 2 SEP 2010 | DOI: 10.1002/cctc.201000197

    Thumbnail image of graphical abstract

    Domain event: Coenzyme A (CoA) analogues are prepared by biotransformation of suitable pantothenamides using immobilized versions of three of the CoA biosynthetic enzymes. This transformation is achieved by fusing the enzymes to cellulose-binding domains (CBD), which allow for their simultaneous purification and immobilization. In this manner, batch and column reactors capable of continuous CoA analogue production can be prepared and successfully used.

  2. Structure–Activity Relationships of Oligocationic, Ammonium-Functionalized Triarylphosphines as Ligands in the Pd-Catalyzed Suzuki–Miyaura Reaction

    Dennis J. M. Snelders, Cornelis van der Burg, Martin Lutz, Anthony L. Spek, Gerard van Koten and Robertus J. M. Klein Gebbink

    Article first published online: 1 SEP 2010 | DOI: 10.1002/cctc.201000232

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    Ligands in charge: The catalytic activity in the Pd-catalyzed Suzuki–Miyaura reaction upon the use of oligocationic, ammonium-functionalized triarylphosphine ligands is governed by the number of cationic charges in the ligand structure, rather than by their steric or electronic properties. Increasing the number of charges increases the preference for the formation of coordinatively unsaturated phosphine–palladium species, which leads to a higher catalytic activity through faster catalyst activation.

  3. New Strategies for e-Beam Characterization of Catalysts

    A. Howie

    Article first published online: 1 SEP 2010 | DOI: 10.1002/cctc.201000171

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    How exciting is it to be ever so slightly ALOOF? We can answer this question by coincidence detection of emitted secondary electrons (SE). From the threshold excitation energy for SE emission, we may determine the surface barrier height at a nanoparticle facet that is skimmed by a focused fast electron beam.

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