4.7 Article Proceedings Paper

Alkene epoxidation by manganese(III) complexes immobilized onto nanostructured carbon CMK-3

Journal

CATALYSIS TODAY
Volume 203, Issue -, Pages 103-110

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cattod.2012.04.018

Keywords

CMK-3; Complex immobilization; Mn(III)porphyrin; Mn(III)salen; Heterogeneous catalysis; Epoxidation

Funding

  1. Fundacao para a Ciencia e a Tecnologia
  2. FEDER [PEst-C/EQB/LA0006/2011, PTDC/CTM/65718/2006]
  3. FCT
  4. Fundação para a Ciência e a Tecnologia [PTDC/CTM/65718/2006] Funding Source: FCT

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New heterogeneous catalysts were prepared through immobilization of Mn(III) complexes onto CMK-3 with different surface treatments. The [Mn(TF5PP)Cl] and [Mn(5-HOsalhd)Cl] complexes were anchored by a microwave-assisted protocol (CAT I and CAT III, respectively) and the Jacobsen catalyst was immobilized using conventional synthesis conditions (CAT II). XPS and FTIR revealed that the CMK-3 target functionalities for immobilization were the surface oxygen groups. XRD showed that the support treatments led to a decrease of its 2D-hexagonal order, but the complex grafting did not induce changes on the microstructure. CAT I was active in the epoxidation of cis-cyclooctene by H2O2, with substrate conversions and epoxide selectivities in the ranges of 38-30% and 100-97%, respectively, in three cycles with almost no complex leaching. CAT II was active in the epoxidation of 6-cyano-2,2-dimethylchromene using m-CPBA/NMO system with a substrate conversion similar to that of the free complex and higher ee %, but with some Mn leaching in the catalytic runs. CAT III was active in the epoxidation of indene, by H2O2, in ethanol with substrate conversions, epoxide selectivities and ee % values in the ranges of 45-37%, 83-86% and 10-12%, respectively. A correlation between the structural properties of the supports and the reaction times could be proposed. These results highlight the potentiality of CMK-3 to act as support for metal complexes with catalytic properties in oxidation reactions. (C) 2012 Elsevier B. V. All rights reserved.

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