Journal
CHEMICAL SCIENCE
Volume 14, Issue 20, Pages 5453-5459Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3sc01077e
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Cation-uptake has been extensively studied in materials science. In this study, the researchers focused on a molecular crystal composed of a charge-neutral polyoxometalate (POM) capsule and discovered the occurrence of cation-coupled electron-transfer reaction. The findings reveal the significance of the POM capsule in cation uptake.
Cation-uptake has been long researched as an important topic in materials science. Herein we focus on a molecular crystal composed of a charge-neutral polyoxometalate (POM) capsule [(Mo72Fe30O252)-Fe-VI-O-III(H2O)(102)(CH3CO2)(15)](3+) encapsulating a Keggin-type phosphododecamolybdate anion [alpha-(PMo12O40)-O-VI](3-). Cation-coupled electron-transfer reaction occurs by treating the molecular crystal in an aqueous solution containing CsCl and ascorbic acid as a reducing reagent. Specifically, multiple Cs+ ions and electrons are captured in crown-ether-like pores {(Mo3Fe3O6)-Fe-VI-O-III}, which exist on the surface of the POM capsule, and Mo atoms, respectively. The locations of Cs+ ions and electrons are revealed by single-crystal X-ray diffraction and density functional theory studies. Highly selective Cs+ ion uptake is observed from an aqueous solution containing various alkali metal ions. Cs+ ions can be released from the crown-ether-like pores by the addition of aqueous chlorine as an oxidizing reagent. These results show that the POM capsule functions as an unprecedented redox-active inorganic crown ether, clearly distinguished from the non-redox-active organic counterpart.
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