Kinetics and mechanism of aluminum(III)/siderophore ligand exchange: mono(deferriferrioxamine B)aluminum(III) formation and dissociation in aqueous acid solution

Published

Journal Article

The kinetics and mechanism of a linear trihydroxamic acid siderophore (deferriferrioxamine B, H4DFB+) ligand exchange with Al(H2O)63+ to form mono(deferriferrioxamine B)aluminum(III) (Al(H2O)4H3DFB)3+ have been investigated at 25 °C over the [H+] range 0.001-1.0 M and I = 2.0 M (HClO4/NaClO4) by 27Al NMR. Kinetic results are consistent with Al(H2O)4(H3DFB)3+ formation and dissociation proceeding through a parallel path mechanistic scheme involving Al(H2O)63+(k2/k-1) and Al(H2O)5(OH)2+(k2/k-2) where k1 = 0.13 M-1 s-1, k-1 = 8.7 × 10-3 M-1 s-1, k2 = 2.7 × 103 M-1 s-1, and k-2 = 9.6 × 10-4 s-1. Relative complex formation rates at Al(H2O)63+ and Al(H2O)5OH2+, and comparison with kinetic data for a series of synthetic hydroxamic acids, suggest that an interchange mechanism is operative. These results are also discussed in relation to kinetic data for the corresponding iron(III)-deferriferrioxamine B system. © 1987.

Full Text

Duke Authors

Cited Authors

  • Mark Garrison, J; Crumbliss, AL

Published Date

  • January 1, 1987

Published In

Volume / Issue

  • 138 / 1

Start / End Page

  • 61 - 65

International Standard Serial Number (ISSN)

  • 0020-1693

Digital Object Identifier (DOI)

  • 10.1016/S0020-1693(00)81182-2

Citation Source

  • Scopus