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Iron(II) Complexes of 2-Mercaptopyridine as Rubredoxin Site Analogues

Abstract

The synthesis, characterization and reactivity studies of iron(II) complexes [FeII(PySH)4](OTf)2, 1-(OTf)2, [FeII(PySH)4](ClO)4, 1-(ClO4)2, and [FeII(PyS)2]n, (2) of 2-mercaptopyridine (PySH) ligand are discussed. The X-ray crystal structures of both 1-(OTf)2, and 1-(ClO4)2 reveal distorted tetrahedral geometry at the iron(II) center with identical constituents. All the pyridine nitrogen atoms are protonated and thiolate ions are coordinated to the iron(II) center. The structure and function of complex 1-(OTf)2 or 1-(ClO4)2 resembles the active site of rubredoxin. Complex 2 has octahedral geometry at the iron(II) center forming a 1-D coordination polymer. Complex 1-(OTf)2 exhibits high positive redox potential (E1/2 = 0.23 V vs Ag/AgCl) which reduces to -0.12 V in the presence of triethylamine under inert atmosphere. This change of redox potential is highly reversible in the presence of weak acid such p-toluenesulfonic acid, pTsOH. DFT studies show that the complex cation [FeII(PySH)4]2+ upon treatment with a base converts to its anionic congener, [FeII(PyS)4]2─ via deprotonation of pyridinium moiety. The iron complexes readily react with molecular oxygen to yield the corresponding iron(III) complex, which rapidly decays to form pyridine disulphide (Py2S2) and an iron(II) complex

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Publication details

The article was received on 20 Jul 2017, accepted on 08 Sep 2017 and first published on 11 Sep 2017


Article type: Paper
DOI: 10.1039/C7DT02645E
Citation: Dalton Trans., 2017, Accepted Manuscript
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    Iron(II) Complexes of 2-Mercaptopyridine as Rubredoxin Site Analogues

    P. Halder, S. Ghorai, S. Banerjee, B. Mondal and A. Rana, Dalton Trans., 2017, Accepted Manuscript , DOI: 10.1039/C7DT02645E

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