Chemistry - A European Journal · 2009 · 29 citations · 43 references
EngineeringRational Monomer DesignSynthetic PhotochemistryOrganic ChemistryChemistryPolymersChemical EngineeringPhotoredox ProcessMacromolecular EngineeringFinal CyclizationPolymer ChemistryMaterials ScienceThree 1,8‐AnthryleneSynthetic MacromoleculePhotochemistrySupramolecular PhotochemistryBiomolecular Engineering1,8-Anthrylene UnitsIterative SynthesisHeterocyclicPolymer SciencePolymer ReactionPolymer Synthesis
An iterative synthesis of a macrocycle with three 1,8-anthrylene units (see picture, R=C6H13) was achieved by using Pd-catalyzed cross-coupling protocols, in which a copper-free Sonogashira reaction was the key to the final cyclization. Photochemical model reactions suggest that the macrocycle has the potential to undergo photo-induced [4+4] cycloaddition without undesired side reactions, which is of relevance for the ultimate goal of creating 2D polymers. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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The structure of suspended graphene sheets
Jannik C. Meyer, A. K. Geǐm, M. I. Katsnelson et al. · Nature · 2007 · 5K citations · Full text