4.2 Article

Halogenated meso-phenyl Mn(III) porphyrins as highly efficient catalysts for the synthesis of polycarbonates and cyclic carbonates using carbon dioxide and epoxides

Journal

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
Volume 423, Issue -, Pages 489-494

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcata.2015.10.025

Keywords

Polycarbonates; Cyclic carbonates; Metalloporphyrins; Manganese(III); Carbon dioxide

Funding

  1. Ministerio de Economia y Competitividad [CTQ2013-43438-R]
  2. Departament d'Economia i Coneixement (Generalitat de Catalunya) [2014SGR 670]
  3. FCT-Portugal (Portuguese Foundation for Science and Technology)
  4. FEDER-European Regional Development Fund through the COMPETE Programme (Operational Programme for Competitiveness) [UID/QUI/00313/2013]
  5. [SFRH/BD/84146/2012]
  6. Fundação para a Ciência e a Tecnologia [SFRH/BD/84146/2012] Funding Source: FCT

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Introduction of halogen electron withdrawing atoms (chloro and fluoro) in the ortho position of the aryl groups of meso-tetraphenylporphyrin manganese(III) complexes increased their activity as catalysts in the reaction of carbon dioxide with epoxides, when compared with the meso-tetraphenylporphyrin manganese(III) counterpart, even in the absence of co-catalysts. In the polymerization reaction of carbon dioxide and cyclohexene oxide, almost ten-fold increase of the TOF was observed when 5,10,15,20-tetra(2,6-dichlorophenyl)porphyrinatomanganese(III) acetate or 5,10,15,20-tetra(2,6-difluorophenyl)porphyrinatomanganese(III) acetate complexes were used as catalysts. Under similar conditions, when terminal epoxides were used as substrates, the selective cycloaddition of CO2 with styrene oxide, epichlorohydrin, propylene oxide, and 1,2-epoxytetradecane yielded exclusively the corresponding cyclic carbonates (conversion 6-98%). (C) 2016 Published by Elsevier B.V.

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