Chemistry – An Asian Journal
Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Editor: Theresa Kueckmann
Impact Factor: 3.935
ISI Journal Citation Reports © Ranking: 2013: 32/148 (Chemistry Multidisciplinary)
Online ISSN: 1861-471X
Associated Title(s): Angewandte Chemie International Edition, Asian Journal of Organic Chemistry, Chemistry - A European Journal, Chinese Journal of Chemistry, Journal of the Chinese Chemical Society, The Chemical Record
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February 01, 2014
New Online Manuscript Submission System
We are pleased to announce that after over ten years, manuscriptXpress was replaced by a new Manuscript handling system, EditorialManager from ARIES, on February 1.
The links to the new journal sites are available at: chemistryviews.org/submission.
Articles that have been submitted to manuscriptXpress will be processed from there.
Thank you for your patience and we look forward to receiving your next excellent manuscript.
Below are the most frequent article keywords in 2013. Click on a keyword to find the latest articles that have it. Click "Edit Search" on the results page to refine or expand the query. Click "Save Search" to add the query to your profile and be alerted to new articles that match it.
copper · density functional calculations · electrochemistry · fluorescence · gold · graphene · heterocycles · homogeneous catalysis · magnetic properties · mesoporous materials · nanoparticles · nanostructures · natural products · organocatalysis · oxidation · self-assembly · sensors · synthetic methods
Recently Published Articles
- Diindolo[2,3-b:2′,3′-f]pyrrolo[3,2-b]pyrroles as Electron-Rich, Ladder-Type Fluorophores: Synthesis and Optical Properties
Dr. Anita Janiga, Maciej Krzeszewski and Prof. Daniel T. Gryko
Article first published online: 1 OCT 2014 | DOI: 10.1002/asia.201402925
Feeling a little blue: Unprecedented heterocycles containing four linearly fused pyrrole moieties are synthesized in three steps from commercially available materials. All these π-expanded pyrrolo[3,2-b]pyrroles display blue emission, and the fluorescence quantum yields are typically over 70 %. The is located at −4.6 to −5.1 eV.
- Copper(II)-Mediated Transformation of a Tridentate Non-Innocent Ligand into a Tetradentate Salen-Type Innocent Ligand
Samir Ghorai and Dr. Chandan Mukherjee
Article first published online: 1 OCT 2014 | DOI: 10.1002/asia.201402868
Radically different: The H4L ligand is a combination of benzylamine, the substrate part, and 4,6-di-tert-butyl-2-aminophenol, the π-radical generating part. It reacts with CuII to provide 1 through ligand-centered amine oxidation, CN bond cleavage, and CO bond formation. H4L2, a geometrical isomer of H4L, and H3L1, the two-electron oxidized (imine) form of H4L2, also provide 1 under the same reaction conditions.
- Enantioselective Radical Alkynylation of C(sp3)-H Bonds Using Sulfoximine as a Traceless Chiral Auxiliary
Dr. Masanori Nagatomo, Shun Yoshioka and Prof. Dr. Masayuki Inoue
Article first published online: 1 OCT 2014 | DOI: 10.1002/asia.201402983
Without a trace: Enantioselective alkynylation of C(sp3)H bonds adjacent to a nitrogen atom has been achieved using only chiral p-tolyl tert-butyldimethylsilylethynyl sulfoximine and benzophenone under photo-irradiation conditions. The NH-unprotected sulfoximine group efficiently transmits its stereochemical information to the product and functions as a traceless chiral auxiliary.
- Polymer- and Silica-Supported Iron BPMEN-Inspired Catalysts for CH Bond Functionalization Reactions
Dr. Yan Feng, Dr. Eric G. Moschetta and Prof. Christopher W. Jones
Article first published online: 1 OCT 2014 | DOI: 10.1002/asia.201402461
Minor adjustments: Two approaches are presented to functionalize the popular N1,N2-dimethyl-N1,N2-bis(pyridin-2-ylmethyl)ethane-1,2-diamine (BPMEN) ligand, so that it can be supported on porous silica or polymer resin supports. Iron that complexes with this ligand can be used in an array of catalytic CH functionalization reactions (see picture).
- Molecular Pop-up Toy: A Molecular Machine Based on Folding/Unfolding Motion of Alkyl Chains Bound to a Host
Dr. Young Ho Ko, Dr. Ilha Hwang, Hyunuk Kim, Youngkook Kim and Prof. Dr. Kimoon Kim
Article first published online: 29 SEP 2014 | DOI: 10.1002/asia.201402988
Alkyl chains in action! A new type of redox-driven molecular machine based on the reversible interconversion between a folded and an extended conformation of an alkyl chain has been designed and synthesized.