Stepwise Assembly of an Electroactive Framework from a Co 6 S 8 Superatomic Metalloligand and Cuprous Iodide Building Units

• Published in: Chemistry : a European journal Vol. 26; no. 55; pp. 12523 - 12527
• Main Authors: Freeman, Matthew B., Edokobi, Ozioma D., Gillen, Jonathan H., Kocherga, Margaret, Dipple, Kathleen M., Jones, Daniel S., Paley, Daniel W., Wang, Le, Bejger, Christopher M.
• Format: Journal Article
• Language: English
• Published: 01.10.2020
• ISSN: 0947-6539; 1521-3765
• DOI: 10.1002/chem.202001215

Abstract The design of metal–organic frameworks (MOFs) that incorporate more than one metal cluster constituent is a challenging task. Conventional one‐pot reaction protocols require judicious selection of ligand and metal ion precursors, yet remain unpredictable. Stable, preformed nanoclusters, with ligand shells that can undergo additional coordination‐driven reactions, provide a platform for assembling multi‐cluster solids with precision. Herein, a discrete Co 6 S 8 (PTA) 6 (PTA=1,3,5‐triaza‐7‐phosphaadamantane) superatomic‐metalloligand is assembled into a three‐dimensional (3D) coordination polymer comprising Cu 4 I 4 secondary building units (SBUs). The resulting heterobimetallic framework ( 1 ) contains two distinct cluster constituents and bifunctional PTA linkers. Solid‐state diffuse reflectance studies reveal that 1 is an optical semiconductor with a band‐gap of 1.59 eV. Framework‐modified electrodes exhibit reversible redox behavior in the solid state arising from the Co 6 S 8 superatoms, which remain intact during framework synthesis.