Coordination-Driven Selective Formation of D Symmetric Octanuclear Organometallic Cages.

The coordination-driven self-assembly of organometallic half-sandwich iridium(III)- and rhodium(III)-based building blocks with asymmetric ambidentate pyridyl-carboxylate ligands is described. Despite the potential for obtaining a statistical mixture of multiple products, D symmetric octanuclear cages were formed selectively by taking advantage of the electronic effects emanating from the two types of chelating sites - (O,O') and (N,N') - on the tetranuclear building blocks. The metal sources and the lengths of bridging ligands influence the selectivity of the self-assembly. Experimental observations, supported by computational studies, suggest that the D symmetric cages are the thermodynamically favored products. Overall, the results underline the importance of electronic effects on the selectivity of coordination-driven self-assembly, and demonstrate that asymmetric ambidentate ligands can be used to control the design of discrete supramolecular coordination complexes.