4.5 Article

Efficient and Selective Oxidation of Primary and Secondary Alcohols Using an Iron(III)/Phenanthroline Complex: Structural Studies and Catalytic Activity

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume -, Issue 28, Pages 4479-4485

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201200658

Keywords

Homogeneous catalysis; Oxidation; Iron; Alcohols; Ketones

Funding

  1. University Grants Commission (UGC), New Delhi, India [MRP] [F. PSW-039/09-10(ERO)]
  2. National Science Council of Taiwan [NSC 99-2113-M-006-003-MY3]
  3. Fonds National de la Recherche Scientifique (FNRS) [FRFC 2.4508.08, FRFC 2.4537.12, IISN 4.4507.10]

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An efficient catalytic system for the oxidation of alcohols has been developed by using iron(III) catalyst [Fe(phen)2Cl2]NO3 (1) (phen = 1,10-phenanthroline) and H2O2 as terminal oxidant. A series of primary and secondary alcohols were oxidized into aldehydes and ketones in good yields and excellent selectivities after a short reaction time. The mononuclear iron(III) complex [Fe(phen)2Cl2]NO3 was characterized by several independent methods. The X-ray structure shows distorted octahedral geometry around the FeIII center, which is in a high-spin state (S = 5/2) according to Mossbauer study.

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