Electrochemical, spectroscopic, and computational study of bis(μ-methylthiolato)diironhexacarbonyl: Homoassociative stabilization of the dianion and a chemically reversible reduction/reoxidation cycle

Orrasa In-Noi, Kenneth J. Haller, Gabriel B. Hall, William P. Brezinski, Jacob M. Marx, Taka Sakamoto, Dennis H. Evans, Richard S Glass, Dennis L Lichtenberger

Research output: Contribution to journalArticle

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Abstract

The redox characteristics of (μ-SMe)<inf>2</inf>Fe<inf>2</inf>(CO)<inf>6</inf> from the 1+ to 2- charge states are reported. This [2Fe-2S] compound is related to the active sites of [FeFe]-hydrogenases but notably without a linker between the sulfur atoms. The 1+ charge state was studied both by ionization in the gas phase by photoelectron spectroscopy and by oxidation in the solution phase by cyclic voltammetry. The adiabatic ionization is to a cation whose structure features a semibridging carbonyl, similar to the structure of the active site of [FeFe]-hydrogenases in the same oxidation state. The reduction of the compound by cyclic voltammetry gives an electrochemically irreversible cathodic peak, which often suggests disproportionation or other irreversible chemical processes in this class of molecules. However, the return scan through electrochemically irreversible oxidation peaks that occur at potentials around 1 V more positive than the reduction led to the recovery of the initial neutral compound. The dependence of the CVs on scan rate, IR spectroelectrochemistry of reduction and oxidation cycles, chronocoulometry, and DFT computations indicate a mechanism in which stabilization of the dianion plays a key role. Initial one-electron reduction of the compound is accompanied in the same cathodic peak with a second slower electron reduction to the dianion. Geometric reorganization and solvation stabilize the [2Fe-2S]<sup>2-</sup> dianion such that the potential for addition of the second electron is slightly less negative than that of the first (potential inversion). The return oxidation peaks at more positive potentials follow from rapid pairing of the dianion with another neutral molecule in solution (termed homoassociation) to form a stabilized [4Fe-4S]<sup>2-</sup> dianion. Two one-electron oxidations of this [4Fe-4S]<sup>2-</sup> dianion result in regeneration of the initial neutral compound. The implications of this homoassociation for the [FeFe]-hydrogenase enzyme, in which the H-cluster active site features a [2Fe-2S] site associated with a [4Fe-4S] cubane cluster via a thiolate bridge, are discussed. (Figure Presented)

Original languageEnglish (US)
Pages (from-to)5009-5019
Number of pages11
JournalOrganometallics
Volume33
Issue number18
DOIs
StatePublished - Sep 22 2014

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Stabilization
stabilization
Hydrogenase
Oxidation
oxidation
cycles
Electrons
Cyclic voltammetry
Ionization
electrons
Spectroelectrochemistry
cubane
ionization
Molecules
Solvation
Carbon Monoxide
Photoelectron spectroscopy
regeneration
Sulfur
Discrete Fourier transforms

ASJC Scopus subject areas

  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Inorganic Chemistry

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Electrochemical, spectroscopic, and computational study of bis(μ-methylthiolato)diironhexacarbonyl : Homoassociative stabilization of the dianion and a chemically reversible reduction/reoxidation cycle. / In-Noi, Orrasa; Haller, Kenneth J.; Hall, Gabriel B.; Brezinski, William P.; Marx, Jacob M.; Sakamoto, Taka; Evans, Dennis H.; Glass, Richard S; Lichtenberger, Dennis L.

In: Organometallics, Vol. 33, No. 18, 22.09.2014, p. 5009-5019.

Research output: Contribution to journalArticle

In-Noi, Orrasa ; Haller, Kenneth J. ; Hall, Gabriel B. ; Brezinski, William P. ; Marx, Jacob M. ; Sakamoto, Taka ; Evans, Dennis H. ; Glass, Richard S ; Lichtenberger, Dennis L. / Electrochemical, spectroscopic, and computational study of bis(μ-methylthiolato)diironhexacarbonyl : Homoassociative stabilization of the dianion and a chemically reversible reduction/reoxidation cycle. In: Organometallics. 2014 ; Vol. 33, No. 18. pp. 5009-5019.
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abstract = "The redox characteristics of (μ-SMe)2Fe2(CO)6 from the 1+ to 2- charge states are reported. This [2Fe-2S] compound is related to the active sites of [FeFe]-hydrogenases but notably without a linker between the sulfur atoms. The 1+ charge state was studied both by ionization in the gas phase by photoelectron spectroscopy and by oxidation in the solution phase by cyclic voltammetry. The adiabatic ionization is to a cation whose structure features a semibridging carbonyl, similar to the structure of the active site of [FeFe]-hydrogenases in the same oxidation state. The reduction of the compound by cyclic voltammetry gives an electrochemically irreversible cathodic peak, which often suggests disproportionation or other irreversible chemical processes in this class of molecules. However, the return scan through electrochemically irreversible oxidation peaks that occur at potentials around 1 V more positive than the reduction led to the recovery of the initial neutral compound. The dependence of the CVs on scan rate, IR spectroelectrochemistry of reduction and oxidation cycles, chronocoulometry, and DFT computations indicate a mechanism in which stabilization of the dianion plays a key role. Initial one-electron reduction of the compound is accompanied in the same cathodic peak with a second slower electron reduction to the dianion. Geometric reorganization and solvation stabilize the [2Fe-2S]2- dianion such that the potential for addition of the second electron is slightly less negative than that of the first (potential inversion). The return oxidation peaks at more positive potentials follow from rapid pairing of the dianion with another neutral molecule in solution (termed homoassociation) to form a stabilized [4Fe-4S]2- dianion. Two one-electron oxidations of this [4Fe-4S]2- dianion result in regeneration of the initial neutral compound. The implications of this homoassociation for the [FeFe]-hydrogenase enzyme, in which the H-cluster active site features a [2Fe-2S] site associated with a [4Fe-4S] cubane cluster via a thiolate bridge, are discussed. (Figure Presented)",
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T2 - Homoassociative stabilization of the dianion and a chemically reversible reduction/reoxidation cycle

AU - In-Noi, Orrasa

AU - Haller, Kenneth J.

AU - Hall, Gabriel B.

AU - Brezinski, William P.

AU - Marx, Jacob M.

AU - Sakamoto, Taka

AU - Evans, Dennis H.

AU - Glass, Richard S

AU - Lichtenberger, Dennis L

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N2 - The redox characteristics of (μ-SMe)2Fe2(CO)6 from the 1+ to 2- charge states are reported. This [2Fe-2S] compound is related to the active sites of [FeFe]-hydrogenases but notably without a linker between the sulfur atoms. The 1+ charge state was studied both by ionization in the gas phase by photoelectron spectroscopy and by oxidation in the solution phase by cyclic voltammetry. The adiabatic ionization is to a cation whose structure features a semibridging carbonyl, similar to the structure of the active site of [FeFe]-hydrogenases in the same oxidation state. The reduction of the compound by cyclic voltammetry gives an electrochemically irreversible cathodic peak, which often suggests disproportionation or other irreversible chemical processes in this class of molecules. However, the return scan through electrochemically irreversible oxidation peaks that occur at potentials around 1 V more positive than the reduction led to the recovery of the initial neutral compound. The dependence of the CVs on scan rate, IR spectroelectrochemistry of reduction and oxidation cycles, chronocoulometry, and DFT computations indicate a mechanism in which stabilization of the dianion plays a key role. Initial one-electron reduction of the compound is accompanied in the same cathodic peak with a second slower electron reduction to the dianion. Geometric reorganization and solvation stabilize the [2Fe-2S]2- dianion such that the potential for addition of the second electron is slightly less negative than that of the first (potential inversion). The return oxidation peaks at more positive potentials follow from rapid pairing of the dianion with another neutral molecule in solution (termed homoassociation) to form a stabilized [4Fe-4S]2- dianion. Two one-electron oxidations of this [4Fe-4S]2- dianion result in regeneration of the initial neutral compound. The implications of this homoassociation for the [FeFe]-hydrogenase enzyme, in which the H-cluster active site features a [2Fe-2S] site associated with a [4Fe-4S] cubane cluster via a thiolate bridge, are discussed. (Figure Presented)

AB - The redox characteristics of (μ-SMe)2Fe2(CO)6 from the 1+ to 2- charge states are reported. This [2Fe-2S] compound is related to the active sites of [FeFe]-hydrogenases but notably without a linker between the sulfur atoms. The 1+ charge state was studied both by ionization in the gas phase by photoelectron spectroscopy and by oxidation in the solution phase by cyclic voltammetry. The adiabatic ionization is to a cation whose structure features a semibridging carbonyl, similar to the structure of the active site of [FeFe]-hydrogenases in the same oxidation state. The reduction of the compound by cyclic voltammetry gives an electrochemically irreversible cathodic peak, which often suggests disproportionation or other irreversible chemical processes in this class of molecules. However, the return scan through electrochemically irreversible oxidation peaks that occur at potentials around 1 V more positive than the reduction led to the recovery of the initial neutral compound. The dependence of the CVs on scan rate, IR spectroelectrochemistry of reduction and oxidation cycles, chronocoulometry, and DFT computations indicate a mechanism in which stabilization of the dianion plays a key role. Initial one-electron reduction of the compound is accompanied in the same cathodic peak with a second slower electron reduction to the dianion. Geometric reorganization and solvation stabilize the [2Fe-2S]2- dianion such that the potential for addition of the second electron is slightly less negative than that of the first (potential inversion). The return oxidation peaks at more positive potentials follow from rapid pairing of the dianion with another neutral molecule in solution (termed homoassociation) to form a stabilized [4Fe-4S]2- dianion. Two one-electron oxidations of this [4Fe-4S]2- dianion result in regeneration of the initial neutral compound. The implications of this homoassociation for the [FeFe]-hydrogenase enzyme, in which the H-cluster active site features a [2Fe-2S] site associated with a [4Fe-4S] cubane cluster via a thiolate bridge, are discussed. (Figure Presented)

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