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Details

Autor(en) / Beteiligte
Titel
Fe() complexes of pyridine-substituted thiosemicarbazone ligands as catalysts for oxidations with hydrogen peroxide
Ist Teil von
  • Dalton transactions : an international journal of inorganic chemistry, 2023-10, Vol.52 (4), p.1466-14612
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2023
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • The reaction of three [Fe II (TSC) 2 ] complexes, where TSC is a pyridine-substituted thiosemicarbazone of the HDpT or HBpT families, with H 2 O 2 in acetonitrile solution does not result in the accumulation of the corresponding [Fe III (TSC) 2 ] + complexes. Instead, a mixture of diamagnetic low-spin Fe II species is generated. According to the MS spectra, those species result from the sequential addition of up to five oxygen atoms to the complex. This capability for the addition of oxygen atoms suggested that oxygen atom transfer to external substrates may be possible, and these TSC complexes were tested in the oxidation of thioanisole and styrene with H 2 O 2 . As hypothesized, the complexes are active in both the oxidation of thioanisole to its sulfoxide and styrene to benzaldehyde, with time scales indicating the participation of the species containing added oxygen atoms. Interestingly, the free thiosemicarbazone ligands and the [Zn(Dp44mT) 2 ] complex also catalyse the selective sulfoxidation of thioanisole, but they are ineffective in catalysing styrene oxidation to benzaldehyde. These findings open up new directions for the development of thiosemicarbazone-based metal catalysts for oxidation processes. [Fe II (TSC) 2 ] complexes selectively catalyze oxidation of styrene to benzaldehyde with H 2 O 2 . These iron complexes, the free TSC ligands, and [Zn(Dp44mT) 2 ] also catalyze sulfoxidation of thioanisole, but only the iron complexes catalyze styrene oxidation.
Sprache
Englisch
Identifikatoren
ISSN: 1477-9226
eISSN: 1477-9234
DOI: 10.1039/d3dt02442c
Titel-ID: cdi_proquest_miscellaneous_2872181754

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