Abstract
A neutral copper complex flanked by two protonated 4,5-diazafluoren-9-one (dafone, 1) ligands which are H-bonded with water molecules and perchlorate anions has been structurally and electrochemically characterized. The capped copper compound remains intact in solution, exhibiting a reversible Cu(II)/Cu(I) couple although undergoing a deformation along the Cu–N(2) axis and can serve as a good model of ionic pockets with metal active sites in some metalloproteins.
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