Abstract
Abstract The incorporation of a transition metal ion into a poly-aza macrocyle favors the access to unusually high oxidation states (e.g. NiIII, CuIII). The tendency to stabilize trivalent cations, which is expressed by the value of the potential of the MIII/MIII redox couple, is regulated by the structural features of the macrocycle (ring size, number and type of the donor nitrogen atoms). In general, formation of trivalent complexes is favored by strong equatorial interactions and the CuII/CuIII oxidation process profits from the ligand-field contribution to a larger extent than does the corresponding NiII/NiIII process. The solvent may profoundly influence the MIII/MIII redox change through axial coordination of one of the redox-active macrocyclic complexes.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.