4.8 Article

Indigo dye production by enzymatic mimicking based on an iron(III)porphyrin

Journal

JOURNAL OF CATALYSIS
Volume 315, Issue -, Pages 33-40

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2014.04.012

Keywords

Indigo; Indole; Iron(Ill)porphyrin; Oxidation; Catalysis; Hydrogen peroxide; Mechanism; Ethanol

Funding

  1. Fundacao para a Ciencia e a Tecnologia (FCT, Portugal)
  2. European Union
  3. QREN
  4. FEDER
  5. COMPETE
  6. REQUIMTE [PEst-C/EQB/LA0006/2011, NORTE-07-0124-FEDER-000067-nanochemistry]
  7. QOPNA [PEst-C/QUI/UI0062/2013, FCOMP-01-0124-FEDER-037296]
  8. Portuguese National NMR Network
  9. FCT

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A novel indigo synthesis is based on a simple and cost-effective model system of the enzymes involved in the natural and biocatalytic productions. The method considers the oxidation of indole by hydrogen peroxide, being catalyzed by an iron(III)porphyrin in ethanol, as solvent, and no other additives. The yields of indigo and of the other oxidized indolinoid derivatives were found to be dependent on the metalloporphyrin system used and on the control of the oxidation conditions. Significant reductions of the environmental impact relatively to the present industrial production and of the costs relatively to the biocatalytic methodologies were obtained. The enhanced indigo production in the presence of the iron(III)porphyrin-ethanol catalytic system relatively to the manganese(III)porphyrin-acetonitrile system can be rationalized by the formation of different active species in the two systems. (C) 2014 Elsevier Inc. All rights reserved.

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