The synthesis of a corrole analogue of aquacobalamin (vitamin B12a) and its ligand substitution reactions
| Autor: | Penny Poomani Govender, Joseph P. Michael, Helder M. Marques, Isabelle Navizet, Manuel A. Fernandes, Sadhna Mathura, Caitlin F. Zipp, Christopher B. Perry |
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| Přispěvatelé: | Molecular Science Institute, School of Chemistry, University of the Witwatersrand [Johannesburg] (WITS), Department of Applied Chemistry [University of Johannesburg], University of Johannesburg (UJ), University of Johannesburg [South Africa] (UJ) |
| Jazyk: | angličtina |
| Rok vydání: | 2014 |
| Předmět: |
Substitution reaction
Aquacobalamin Magnetic Resonance Spectroscopy Porphyrins Stereochemistry Ligand Vitamin B12a chemistry.chemical_element Ligands Inorganic Chemistry [CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry Vitamin B 12 chemistry.chemical_compound Monomer X-Ray Diffraction chemistry Spectrophotometry Ultraviolet Physical and Theoretical Chemistry Corrole Cobalt Equilibrium constant |
| Zdroj: | Inorganic Chemistry Inorganic Chemistry, American Chemical Society, 2014, 53 (9), pp.4418-29. ⟨10.1021/ic5000793⟩ |
| ISSN: | 0020-1669 1520-510X |
| DOI: | 10.1021/ic5000793⟩ |
| Popis: | International audience; The synthesis of a Co(III) corrole, [10-(2-[[4-(1H-imidazol-1-ylmethyl)benzoyl]amino]phenyl)-5,15-diphenylcorrolato]cobalt(III), DPTC-Co, bearing a tail motif terminating in an imidazole ligand that coordinates Co(III), is described. The corrole therefore places Co(III) in a similar environment to that in aquacobalamin (vitamin B12a, H2OCbl(+)) but with a different equatorial ligand. In coordinating solvents, DPTC-Co is a mixture of five- and six-coordinate species, with a solvent molecule occupying the axial coordination site trans to the proximal imidazole ligand. In an 80:20 MeOH/H2O solution, allowed to age for about 1 h, the predominant species is the six-coordinate aqua species [H2O-DPTC-Co]. It is monomeric at least up to concentrations of 60 μM. The coordinated H2O has a pKa = 9.76(6). Under the same conditions H2OCbl(+) has a pKa = 7.40(2). Equilibrium constants for the substitution of coordinated H2O by exogenous ligands are reported as log K values for neutral N-, P-, and S-donor ligands, and CN(-), NO2(-), N3(-), SCN(-), I(-), and Cys in 80:20 MeOH/H2O solution at low ionic strength. The log K values for [H2O-DPTC-Co] correlate reasonably well with those for H2OCbl(+); therefore, Co(III) displays a similar behavior toward these ligands irrespective of whether the equatorial ligand is a corrole or a corrin. Pyridine is an exception; it is poorly coordinated by H2OCbl(+) because of the sterically hindered coordination site of the corrin. With few exceptions, [H2O-DPTC-Co] has a higher affinity for neutral ligands than H2OCbl(+), but the converse is true for anionic ligands. Density functional theory (DFT) models (BP86/TZVP) show that the Co-ligand bonds tend to be longer in corrin than in corrole complexes, explaining the higher affinity of the latter for neutral ligands. It is argued that the residual charge at the metal center (+2 in corrin, 0 in corrole) increases the affinity of H2OCbl(+) for anionic ligands through an electrostatic attraction. The topological properties of the electron density in the DFT-modeled compounds are used to explore the nature of the bonding between the metal and the ligands. |
| Databáze: | OpenAIRE |
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