Ligand-Protecting Strategy for the Controlled Construction of Multinuclear Copper Cores within a Ring-Shaped Polyoxometalate
Yoshihiro Koizumi, Kentaro Yonesato, Kazuya Yamaguchi, Kosuke Suzuki
Abstract
The ring-shaped polyoxometalate (POM) [P8W48O184]40– contains a large cavity and is an attractive inorganic multidentate ligand for accumulating metal cations. Until now, several multinuclear metal cores are constructed within the {P8W48} framework in aqueous solvents. However, it is still challenging to control the number and arrangement of introduced metal cations because of the numerous coordination sites inside the {P8W48} framework. In this study, we developed a novel approach for the selective synthesis of several multinuclear copper-containing ring-shaped POMs in organic solvents using methoxy groups as organic protecting ligands for the reactive coordination sites. Reacting a tetra-n-butylammonium (TBA) salt of [P8W48O184]40– (P8W48) with 4 and 8 equiv of copper(II) acetate in the presence of methanol (MeOH), tetra- and octacopper cores were incorporated into the cavity to form TBA11H13[Cu4(H2O)4P8W48O176(OCH3)8]·28H2O·3CH3NO2 (Cu4) and TBA14H2[Cu8(H2O)12P8W48O176(OCH3)8]·24H2O·CH3CN (Cu8), respectively. For both structures, methoxy groups served as protecting ligands and temporarily inactivated vacant coordination sites. Without MeOH, dodeca- and hexadecacopper cores were constructed inside the cavity to form TBA14H2[Cu12(H2O)16P8W48O184]·4H2O (Cu12) and TBA16H8[Cu16(OH)16(H2O)4P8W48O184]·12H2O·C3H6O (Cu16), respectively. The arrangement of copper ions on the same {P2W12} units could be controlled by the input number of copper ions. Moreover, all four POMs could be synthesized from P8W48 by the stepwise addition of 4 equiv of copper(II) acetate, clarifying the introduction process.