Literature DB >> 24446331

Highly active aluminium catalysts for the formation of organic carbonates from CO2 and oxiranes.

Christopher J Whiteoak1, Nicola Kielland, Victor Laserna, Fernando Castro-Gómez, Eddy Martin, Eduardo C Escudero-Adán, Carles Bo, Arjan W Kleij.   

Abstract

Al(III) complexes of amino-tris(phenolate) ligand scaffolds have been prepared to attain highly Lewis acidic catalysts. Combination of the aforementioned systems with ammonium halides provides highly active catalysts for the synthesis of organic carbonates through addition of carbon dioxide to oxiranes with initial turnover frequencies among the highest reported to date within the context of cyclic carbonate formation. Density functional theory (DFT) studies combined with kinetic data provides a rational for the relative high activity found for these Al(III) complexes, and the data are consistent with a monometallic mechanism. The activity and versatility of these Al(III) complexes has also been evaluated against some state-of-the-art catalysts and the combined results compare favorably in terms of catalyst construction, stability, activity, and applicability.
Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  aluminium; carbon dioxide; carbonates; homogeneous catalysis; ligands

Year:  2014        PMID: 24446331     DOI: 10.1002/chem.201302536

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Aluminium based binary catalytic system for the solvent free conversion of CO2 to carbonates with high activity and selectivity.

Authors:  Ran Ma; Haojie Sun; Yuanzhi Cui
Journal:  RSC Adv       Date:  2018-03-21       Impact factor: 4.036

2.  Comparing kinetic profiles between bifunctional and binary type of Zn(salen)-based catalysts for organic carbonate formation.

Authors:  Carmen Martín; Arjan W Kleij
Journal:  Beilstein J Org Chem       Date:  2014-08-08       Impact factor: 2.883

  2 in total

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