Mikata, Yuji, Kuroda, Yasuko, Naito, Kyoko, Murakami, Kana, Yamamoto, Chihiro, Yabe, Shoko, Yonemura, Shizuka, Matsumoto, Arimasa, and Katano, Hajime
Seven new bis(μ-oxo)dimanganese complexes with Mn2(III , III) or Mn2(III , IV) oxidation states were prepared using quinoline- and isoquinoline-based tetraamine ligands. The structures of the ligands include ethylenediamine, trans-1,2-cyclohexanediamine and tripodal amine, bearing two or three nitrogen-containing heteroaromatics. Regardless of the skeleton and number of aliphatic nitrogen atoms in the ligands, quinoline complexes stabilize the Mn2(III , III) oxidation state, whereas, isoquinoline ligands afford Mn2(III , IV) complexes. A systematic comparison of the differences in structural parameters and redox potentials of a total of 14 complexes with a (μ-O)2Mn2 diamond core, which includes corresponding pyridine and quinoxaline derivatives as supporting ligands, highlights the distinct deviation of quinoline and tripodal amine motifs in this ligand series. [ABSTRACT FROM AUTHOR]