Axial ligand exchange of N-heterocyclic cobalt(III) schiff base complexes: Molecular structure and NMR solution dynamics

Lisa M. Manus, Robert J. Holbrook, Tulay A. Atesin, Marie Heffern, Allison S. Harney, Amanda L. Eckermann, Thomas J. Meade

Research output: Contribution to journalArticle

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Abstract

The kinetic and thermodynamic ligand exchange dynamics are important considerations in the rational design of metal-based therapeutics and therefore, require detailed investigation. Co(III) Schiff base complex derivatives of bis(acetylacetone)ethylenediimine [acacen] have been found to be potent enzyme and transcription factor inhibitors. These complexes undergo solution exchange of labile axial ligands. Upon dissociation, Co(III) irreversibly interacts with specific histidine residues of a protein, and consequently alters structure and causes inhibition. To guide the rational design of next generation agents, understanding the mechanism and dynamics of the ligand exchange process is essential. To investigate the lability, pH stability, and axial ligand exchange of these complexes in the absence of proteins, the pD-and temperature-dependent axial ligand substitution dynamics of a series of N-heterocyclic [Co(acacen)(X)2]+ complexes [where X = 2-methylimidazole (2MeIm), 4-methylimidazole (4MeIm), ammine (NH3), N-methylimidazole (NMeIm), and pyridine (Py)] were characterized by NMR spectroscopy. The pD stability was shown to be closely related to the nature of the axial ligand with the following trend toward aquation: 2MeIm > NH3 4MeIm > Py > Im > NMeIm. Reaction of each [Co(III)(acacen)(X)2] + derivative with 4MeIm showed formation of a mixed ligand Co(III) intermediate via a dissociative ligand exchange mechanism. The stability of the mixed ligand adduct was directly correlated to the pD-dependent stability of the starting Co(III) Schiff base with respect to [Co(acacen)(4MeIm) 2]+. Crystal structure analysis of the [Co(acacen)(X) 2]+ derivatives confirmed the trends in stability observed by NMR spectroscopy. Bond distances between the Co(III) and the axial nitrogen atoms were longest in the 2MeIm derivative as a result of distortion in the planar tetradentate ligand, and this was directly correlated to axial ligand lability and propensity toward exchange.

Original languageEnglish (US)
Pages (from-to)1069-1076
Number of pages8
JournalInorganic Chemistry
Volume52
Issue number2
DOIs
StatePublished - Jan 18 2013
Externally publishedYes

Fingerprint

Schiff Bases
Cobalt
Molecular structure
imines
4-methylimidazole
molecular structure
cobalt
Nuclear magnetic resonance
Ligands
nuclear magnetic resonance
ligands
acetylacetone
Derivatives
Nuclear magnetic resonance spectroscopy
pyridines
Ion exchange
ammines
proteins
trends
histidine

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Physical and Theoretical Chemistry

Cite this

Manus, L. M., Holbrook, R. J., Atesin, T. A., Heffern, M., Harney, A. S., Eckermann, A. L., & Meade, T. J. (2013). Axial ligand exchange of N-heterocyclic cobalt(III) schiff base complexes: Molecular structure and NMR solution dynamics. Inorganic Chemistry, 52(2), 1069-1076. https://doi.org/10.1021/ic302379j

Axial ligand exchange of N-heterocyclic cobalt(III) schiff base complexes : Molecular structure and NMR solution dynamics. / Manus, Lisa M.; Holbrook, Robert J.; Atesin, Tulay A.; Heffern, Marie; Harney, Allison S.; Eckermann, Amanda L.; Meade, Thomas J.

In: Inorganic Chemistry, Vol. 52, No. 2, 18.01.2013, p. 1069-1076.

Research output: Contribution to journalArticle

Manus, Lisa M. ; Holbrook, Robert J. ; Atesin, Tulay A. ; Heffern, Marie ; Harney, Allison S. ; Eckermann, Amanda L. ; Meade, Thomas J. / Axial ligand exchange of N-heterocyclic cobalt(III) schiff base complexes : Molecular structure and NMR solution dynamics. In: Inorganic Chemistry. 2013 ; Vol. 52, No. 2. pp. 1069-1076.
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