Immobilised molecular catalysts and the role of the supporting metal substrate

This work demonstrates that immobilising molecular catalysts on metal substrates can attenuate their reactivity. In particular, the reactivity towards molecular oxygen of both ruthenium tetraphenyl porphyrin (Ru-TPP) and its Ti analogue (Ti-TPP) on Ag(111) was studied as benchmark for the interaction strength of such metal-organic complexes with possible reactants. Here, Ru-TPP proves to be completely unreactive and Ti-TPP strongly reactive towards molecular oxygen; along with comparison to work in the literature, this suggests that studies into immobilised catalysts might find fruition in considering species traditionally seen as too strongly interacting.