Abstract
Molecular photosensitizers that are able to
store multiple reducing equivalents are of great interest in the field of solar
fuel production, where most reactions involve multielectronic reduction processes.
In order to increase the reducing power of a ruthenium tris-diimine charge-photoaccumulating complex, two structural modifications on its fused dipyridophenazine-pyridoquinolinone
ligand were computationally investigated. Addition of an electron-donating oxime group was calculated to substantially decrease the reduction potentials of
the complex, thus guiding the synthesis of a pyridoquinolinone-oxime
derivative. Its spectroscopic and (spectro)electrochemical characterizations
experimentally confirmed the DFT predictions, especially with the first and
second reduction processes cathodically-shifted by −0.24 and −0.14 V, respectively,
compared to the parent complex. Moreover, the ability of this novel artificial
photosynthetic system to store two photogenerated electrons at a more reducing
potential, via a proton-coupled electron transfer mechanism, was demonstrated.
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