“…By adequate substitution of the tripodal platform, it is relatively easy to fine-tune the (i) metal ion binding ability, (ii) the electronic structure and steric environment of the metal centers, and (iii) the nuclearity of the forming complexes. Indeed, by varying the substituents of the tripodal platforms, such ligands form both mono- [5][6][7][8][9][10][11][12] and oligonuclear [7,8,[10][11][12] complexes, and provide tight binding for a range of metal ions, from Cu(I) [8], Cu(II) [9,12], Zn(II) [7,10,11] to Fe(III) [6].…”