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 [MoVI72FeIII30O252(H2O)102(CH3CO2)15]3+ encapsulating a Keggin-type phosphododecamolybdate anion [α-PMoVI12O40]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 {MoVI3FeIII3O6}, 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.
Inglés
00 - Ciencia y conocimiento. Investigación. Cultura. Humanidades
Química
7 p.
Royal Society of Chemistry
JSPS Grants-in-Aid for Scientific Research JP19K23648, JP19H04564, JP19H04686, JP20H02750, and core-to-core program on “International Network on Polyoxometalate Science for Advanced Functional Energy Materials” from MEXT of Japan
ICIQ Foundation, CERCA Program and AGAUR (grant 2017SGR00290) of the Generalitat de Catalunya
Spanish Ministerio de Ciencia e Innovacion through projects PID2020-112806RB-I00 and the Severo Ochoa Excellence Accreditation 2020–2023 CEX2019-000925-S
Creative Commons. Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)
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