Direct assembly of a metallodendrimer encompassing seven triruthenium clusters units

Abstract A general strategy for the assembly of dendrimeric metallo-cluster species based on tritopic trinuclear ruthenium acetate complexes is demonstrated. First, a central core consisting of a [Ru 3 O(CH 3 COO) 6 (TPEB) 3 ]PF 6 complex ( G0 ), where TPEB is the tripodal 1,3,5-tri-4-pyridyl-1,2-ethenylbenzene ligand, was synthesized and then reacted with the end-capping complex [Ru 3 O(CH 3 COO) 6 (py) 2 (MeOH)]PF 6 , thus composing the first generation shell of a dendrimer encompassing twenty-one ruthenium ions ( G1 ). The core and dendrimeric complexes were characterized by elemental analysis, UV–Vis, 1 H NMR, ESI-MS spectrometry and Differential pulse voltammetry. All results were consistent with the structure of that multinuclear cationic dendrimeric species. The isotopologic profile of daughter fragments and the strength of the metal–ligand bonds were carefully investigated providing the fragmentation pathway for the metallo-dendrimer upon ESI-MS dissociation conditions.