High-valent oxo, methoxorhenium complexes: Models for intermediates and transition states in proton-coupled multi-electron transfer reactions

M. S. Ram, Lisa M. Skeens-Jones, Christopher S. Johnson, Xiao Lian Zhang, Charlotte Stern, Dong I. Yoon, Donald Selmarten, Joseph T Hupp

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Abstract

trans-Dioxorhenium(V) tetrapyridyl species are currently under active investigation as model systems for interfacial two-electron, two-proton transfer reaction sequences (Jones-Skeens et al. Inorg. Chem. 1992, 31, 3879). We now find that the corresponding oxo, methoxo complexes can be prepared from the dioxo species and methyl trifluoromethanesulfonate. The new complexes behave nearly identically with the analogous oxo, hydroxo complexes - with one important exception: CH3+, unlike H+, does not dissociate from the oxo ligand. As a direct consequence, the usually elusive rhenium oxidation state IV is stabilized with respect to redox disproportionation and is observable for several complexes at high pH. The ability to detect this state, in turn leads to (1) direct access to the formal reduction potentials for the isolated le- redox couples comprising the overall two-electron transfer (key information for understanding multi-electron transfer kinetics), (2) elucidation of the profound structural and energetic consequences of the initial protonation (methylation) step in the dioxorhenium(V) reduction kinetics, (3) estimates for pKa of (O)(HO)ReVIL43+ (exceptionally negative), and (4) estimates for the first pKa of (HO)2ReIIIL4+ (extremely large and positive). The combination of (1) and (2), in principle, provides sufficient information to characterize completely the energetic accessibility of key intermediate species lying just before or just after the transition state for the two-electron, two-proton reduction of dioxorhenium(V) at electrochemical interfaces.

Original languageEnglish
Pages (from-to)1411-1421
Number of pages11
JournalJournal of the American Chemical Society
Volume117
Issue number4
Publication statusPublished - Feb 1 1995

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Electron transitions
Protons
Electrons
Oxidation-Reduction
Rhenium
Kinetics
Proton transfer
Methylation
Protonation
Ligands
Oxidation

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

High-valent oxo, methoxorhenium complexes : Models for intermediates and transition states in proton-coupled multi-electron transfer reactions. / Ram, M. S.; Skeens-Jones, Lisa M.; Johnson, Christopher S.; Zhang, Xiao Lian; Stern, Charlotte; Yoon, Dong I.; Selmarten, Donald; Hupp, Joseph T.

In: Journal of the American Chemical Society, Vol. 117, No. 4, 01.02.1995, p. 1411-1421.

Research output: Contribution to journalArticle

Ram, M. S. ; Skeens-Jones, Lisa M. ; Johnson, Christopher S. ; Zhang, Xiao Lian ; Stern, Charlotte ; Yoon, Dong I. ; Selmarten, Donald ; Hupp, Joseph T. / High-valent oxo, methoxorhenium complexes : Models for intermediates and transition states in proton-coupled multi-electron transfer reactions. In: Journal of the American Chemical Society. 1995 ; Vol. 117, No. 4. pp. 1411-1421.
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