Solution chemistry of transition metal complexes can be very complicated and difficult to study. The establishment of equilibria depends on the nature of the specific metal ion, its kinetic lability, the thermodynamic stability of the complexes, its oxidation state, the coordinating capability of the solvent where the complexes are dissolved, etc. In fact, while solid complexes represent a "frozen image" of a changing situation, solution chemistry represents a mutating system which can be influenced by a series of factors. A case study to describe the solution chemistry of transition metal ions is represented by vanadium. The solution chemistry of its most important oxidation states, +IV and +V, has been widely investigated because two specific spectroscopic techniques are available: 51V NMR (Nuclear Magnetic Resonance) for V(V) and EPR (Electron Paramagnetic Resonance or ESR, Electron Spin Resonance) for V(IV). In fact, V(V) has no unpaired electrons and can be studied with NMR, while V(IV) has a 3d1 electronic configuration which makes it suitable for EPR spectroscopy. These two techniques permitted the detailed investigation of the solution chemistry of these two oxidation states of the metal and the obtained information is complementary because the two techniques have different limitations. When a specific vanadium complex is dissolved in solution different equiibria can take place: i) redox reactions with interconversion between the two oxidation states; ii) ligand exchange, depending on the thermodynamic stability of the complexes; iii) hydrolysis reactions, with eventual polymerization and/or precipitation of hydroxydes; iv) equilibria between different geometries of the complexes; v) eventual exchange reactions with coordinating solvents. Solution chemistry of vanadium complexes will be discussed in comparison with other transition metal ions. The conclusions drawn for vanadium complexes will be extended to other metal ions which have similar features, while for those which significantly differ from it, the possible scenarios will be depicted.
Solution Chemistry of Transition Metal Complexes: A Case Study of Vanadium
Daniele Sanna
2018
Abstract
Solution chemistry of transition metal complexes can be very complicated and difficult to study. The establishment of equilibria depends on the nature of the specific metal ion, its kinetic lability, the thermodynamic stability of the complexes, its oxidation state, the coordinating capability of the solvent where the complexes are dissolved, etc. In fact, while solid complexes represent a "frozen image" of a changing situation, solution chemistry represents a mutating system which can be influenced by a series of factors. A case study to describe the solution chemistry of transition metal ions is represented by vanadium. The solution chemistry of its most important oxidation states, +IV and +V, has been widely investigated because two specific spectroscopic techniques are available: 51V NMR (Nuclear Magnetic Resonance) for V(V) and EPR (Electron Paramagnetic Resonance or ESR, Electron Spin Resonance) for V(IV). In fact, V(V) has no unpaired electrons and can be studied with NMR, while V(IV) has a 3d1 electronic configuration which makes it suitable for EPR spectroscopy. These two techniques permitted the detailed investigation of the solution chemistry of these two oxidation states of the metal and the obtained information is complementary because the two techniques have different limitations. When a specific vanadium complex is dissolved in solution different equiibria can take place: i) redox reactions with interconversion between the two oxidation states; ii) ligand exchange, depending on the thermodynamic stability of the complexes; iii) hydrolysis reactions, with eventual polymerization and/or precipitation of hydroxydes; iv) equilibria between different geometries of the complexes; v) eventual exchange reactions with coordinating solvents. Solution chemistry of vanadium complexes will be discussed in comparison with other transition metal ions. The conclusions drawn for vanadium complexes will be extended to other metal ions which have similar features, while for those which significantly differ from it, the possible scenarios will be depicted.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.