Ionic Nanoparticle Networks as Solid State Catalysts

We report on the catalytic activity for the cycloaddition of CO2 to cyclic organic carbonates of recently developed ionic nanoparticle networks (INN). The combination of high imidazolium content and ability to coordinate to CO2 molecules within the 3D network makes the hybrid INN materials highly pr...

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Bibliographic Details
Published inEuropean journal of inorganic chemistry Vol. 2012; no. 32; pp. 5305 - 5311
Main Authors Roeser, Jérôme, Kronstein, Martin, Litschauer, Marco, Thomas, Arne, Neouze, Marie-Alexandra
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.11.2012
WILEY‐VCH Verlag
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Summary:We report on the catalytic activity for the cycloaddition of CO2 to cyclic organic carbonates of recently developed ionic nanoparticle networks (INN). The combination of high imidazolium content and ability to coordinate to CO2 molecules within the 3D network makes the hybrid INN materials highly promising heterogeneous catalysts for CO2 activation reactions. The catalytic activity of INN powders and gels was investigated with various starting epoxides. Quantitative conversion was reached with epichlorohydrin. The influence of mono or bis(imidazolium) bridging ligands and methylation at the C2 position in the aromatic ring of the organic cation could be highlighted by evaluation of the activity with the less reactive propylene oxide as the starting epoxide. Finally, the influence of the type of inorganic nanoparticle support was also studied by preparing heterobimetallic silica‐zinc oxide nanoparticle networks. Promising results were obtained with various epoxides. Conversion or selectivity up to 100 % could be obtained. The catalyst could be reused owing to the good thermal stability of the hybrid inorganic‐organic INN. After four reaction runs the catalyst still proved to be active. The catalytic activity of imidazolium‐based nanoparticle networks was demonstrated for CO2 cycloaddition reactions to various epoxides. The hybrid solid‐state material can be easily separated and reused after the reaction. Conversion or selectivity up to 100 % could be obtained under mild conditions and in a short reaction time.
Bibliography:ark:/67375/WNG-MZ0Z4GLP-Z
istex:A99681DBDBB67071BA9B728A3A1C9C6C47D122A6
ArticleID:EJIC201200581
ISSN:1434-1948
1099-0682
DOI:10.1002/ejic.201200581