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Department of Physics and Chemistry
Asymmetric Organic Synthesis and Drug Synthesis Laboratory
1. Journal Articles
Unlocking High Porosity: Post-Synthetic Solvothermal Treatment of Cu-Paddlewheel Based Metal–Organic Cages
Lee, Byeongchan
;
Go, Bogyeong
;
Jung, Byunghyuck
;
Park, Jinhee
Department of Physics and Chemistry
Asymmetric Organic Synthesis and Drug Synthesis Laboratory
1. Journal Articles
Department of Physics and Chemistry
Organic-Inorganic Hybrids Lab
1. Journal Articles
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Title
Unlocking High Porosity: Post-Synthetic Solvothermal Treatment of Cu-Paddlewheel Based Metal–Organic Cages
Issued Date
2024-06
Citation
Lee, Byeongchan. (2024-06). Unlocking High Porosity: Post-Synthetic Solvothermal Treatment of Cu-Paddlewheel Based Metal–Organic Cages. Small, 20(23). doi: 10.1002/smll.202308393
Type
Article
Author Keywords
cage compounds
;
microporous materials
;
solvothermal treatment
;
heterogeneous catalysis
;
metal-organic cages
Keywords
RECOGNITION
;
FRAMEWORKS
;
SURFACE
ISSN
1613-6810
Abstract
Metal–organic cages (MOCs) have garnered significant attention due to their unique discrete structures, intrinsic porosity, designability, and tailorability. However, weak inter-cage interactions, such as van der Waals forces and hydrogen bonding can cause solid-state MOCs to lose structural integrity during desolvation, leading to the loss of porosity. In this work, a novel strategy to retain the permanent porosity of Cu-paddlewheel-based MOCs, enabling their use as heterogeneous catalysts is presented. Post-synthetic solvothermal treatments in non-coordinating solvents, mesitylene, and p-xylene, effectively preserve the packing structures of solvent-evacuated MOCs while preventing cage agglomeration. The resulting MOCs exhibit an exceptional N2 sorption capacity, with a high surface area (SBET=1934m2g−1 for MOP-23), which is among the highest reported for porous MOCs. Intriguingly, while the solvothermal treatment reduced Cu(II) to Cu(I) in the Cu-paddlewheel clusters, the MOCs with mixed-valenced Cu(I)/Cu(II) maintained their crystallinity and permanent porosity. The catalytic activities of these MOCs are successfully examined in copper(I)-catalyzed hydrative amide synthesis, highlighting the prospect of MOCs as versatile reaction platforms. © 2023 Wiley-VCH GmbH.
URI
http://hdl.handle.net/20.500.11750/47654
DOI
10.1002/smll.202308393
Publisher
Wiley
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