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Metal-centred or ligand-based? Catholyte and anolyte redox reactions of actinyl(VI) complexes with open- and
Koichiro Takao1, Tomoyuki Takeyama2, Robert Gericke3
1Laboratory for Zero-Carbon Energy, Institute of Integrated Research, Institute of Science Tokyo, 2-12-1 N1-32, O-okayama, Meguro-ku, 152-8550 Tokyo, Japan. ktakao@zc.iir.isct.ac.jp.
Abstract:
Using a N3O2-pentadentate chelating scaffold (saldien2-) decorated with tBu substituents for steric protection of its oxidized radical enables two chemically reversible redox reactions at both the metal centre and ligand side of actinyl(VI) (AnVIO22+) complexes, regardless of the absence (An = U) or presence (An = Pu) of 5f valence electrons.
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