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   <subfield code="a">A novel iron-enhanced pathway for base-catalyzed catechol oxidation by dioxygen</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Zoltán May, László I. Simándi, and Attila Vértes]</subfield>
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   <subfield code="a">Summary: The kinetics and mechanisms of the catecholase-type biomimetic activation of O2 by the new dioximatoiron(II) complexes [Fe(Hdmed)]+, [Fe(Hdmpd)]+ and [Fe(H2dmdt)]2+ have been studied in methanol. Kinetic measurements reveal first order behavior with respect to catalyst and O2 and a saturation type dependence on the 3,5-di-tert-butylcatechol (H2dtbc) substrate. Added triethylamine increases the rate by changing the reaction mechanism. An important, hitherto unknown feature is iron(II)-enhanced base catalysis of H2dtbc oxidation, via coordination of HdtbcO2- to the Fe(II) complex present, resulting in a significant acceleration of oxidation. A mechanism involving free radicals is suggested on grounds of ESR evidence. The activity pattern of the catalyst complexes correlates with coordination number and symmetry as revealed by Mössbauer spectra.</subfield>
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   <subfield code="a">oxidation kinetics</subfield>
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   <subfield code="a">Mössbauer spectra</subfield>
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   <subfield code="D">Zoltán</subfield>
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   <subfield code="D">and Attila</subfield>
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   <subfield code="t">Reaction Kinetics and Catalysis Letters</subfield>
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