One of the outstanding chemical problems associated with the biological importance of aluminium is the definition of speciation profiles for Al 3c in biological fluids. By speciation profiles is meant the distribution of A13’ among its different complexes, and their structures, stability constants and rates of formation and breakdown. As is often the case with metal speciation, it is the complexes formed with small ligands that present most experimental difficulties. A procedure is described for characterizing speciation profiles for A13+ complexed to small organic ligands, the approach being illustrated with the A13+-heidi system. It is shown that comparative solution NMR and potentiometric studies are in reasonable agreement concerning the number and identity of the major Al 3+-heidi components present in a solution, but the exact structures of the major species are uncertain in some cases. The main approach to determining such structures involves X-ray diffraction studies of crystals obtained from the given solutions, but whether the crystalline forms represent a thermodynamically preferred species in solution is not always clear. Bridging the gap between solid and solution structures is shown to be problematic, even with the comparative vibrational spectroscopies and solidstate NMR.

Defining speciation profile of Al3+ complexed with small organic ligands: the Al3+/Heidi system

TAPPARO, ANDREA
1996

Abstract

One of the outstanding chemical problems associated with the biological importance of aluminium is the definition of speciation profiles for Al 3c in biological fluids. By speciation profiles is meant the distribution of A13’ among its different complexes, and their structures, stability constants and rates of formation and breakdown. As is often the case with metal speciation, it is the complexes formed with small ligands that present most experimental difficulties. A procedure is described for characterizing speciation profiles for A13+ complexed to small organic ligands, the approach being illustrated with the A13+-heidi system. It is shown that comparative solution NMR and potentiometric studies are in reasonable agreement concerning the number and identity of the major Al 3+-heidi components present in a solution, but the exact structures of the major species are uncertain in some cases. The main approach to determining such structures involves X-ray diffraction studies of crystals obtained from the given solutions, but whether the crystalline forms represent a thermodynamically preferred species in solution is not always clear. Bridging the gap between solid and solution structures is shown to be problematic, even with the comparative vibrational spectroscopies and solidstate NMR.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/123543
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