A Gas‐Phase CanMn4−nO4+ Cluster Model for the Oxygen‐Evolving Complex of Photosystem II
Abstract One of the fundamental processes in nature, the oxidation of water, is catalyzed by a small CaMn 3 O 4 ⋅MnO cluster located in photosystem II (PS II). Now, the first successful preparation of a series of isolated ligand‐free tetrameric Ca n Mn 4− n O 4 + ( n =0–4) cluster ions is reported, which are employed as structural models for the catalytically active site of PS II. Gas‐phase reactivity experiments with D 2 O and H 2 18 O in an ion trap reveal the facile deprotonation of multiple water molecules via hydroxylation of the cluster oxo bridges for all investigated clusters. However, only the mono‐calcium cluster CaMn 3 O 4 + is observed to oxidize water via elimination of hydrogen peroxide. First‐principles density functional theory (DFT) calculations elucidate mechanistic details of the deprotonation and oxidation reactions mediated by CaMn 3 O 4 + as well as the role of calcium.