In plants, solar energy is used to extract electrons from water, producing
atmospheric oxygen. This is conducted by Photosystem II, where a redox "tri
ad" consisting of chlorophyll, a tyrosine, and a manganese cluster, governs
an essential part of the process. Photooxidation of the chlorophylls produ
ces electron transfer from the tyrosine, which forms a radical. The radical
and the manganese cluster together extract electrons from water, providing
the biosphere with an unlimited electron source. As a partial model for th
is system we constructed a ruthenium(II) complex with a covalently attached
tyrosine, where the photooxidized ruthenium was rereduced by the tyrosine.
In this study we show that the tyrosyl radical, which gives a transient EP
R signal under illumination, can oxidize a manganese complex. The dinuclear
manganese complex, which initially is in the Mn(III)/(III) state, is oxidi
zed by the photogenerated tyrosyl radical to the Mn(III)/(TV) state. The re
dox potentials in our system are comparable to those in Photosystem II. Thu
s, our synthetic redox "triad" mimics important elements in the electron do
nor "triad" in Photosystem II, significantly advancing the development of s
ystems for artificial photosynthesis based on ruthenium-manganese complexes
.