Lee Byeongchan, Go Bogyeong, Jung Byunghyuck, Park Jinhee
Department of Physics and Chemistry, Daegu Gyeongbuk Institute of Science and Technology (DGIST), 333 Techno Jungang-daero, Dalseong-gun, Daegu, 42988, Republic of Korea.
Small. 2024 Jun;20(23):e2308393. doi: 10.1002/smll.202308393. Epub 2023 Dec 27.
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 N sorption capacity, with a high surface area (S = 1934 m g 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.
金属有机笼状物(MOCs)因其独特的离散结构、固有孔隙率、可设计性和可定制性而备受关注。然而,笼间相互作用较弱,如范德华力和氢键,会导致固态MOCs在去溶剂化过程中失去结构完整性,从而导致孔隙率丧失。在这项工作中,提出了一种保留基于铜桨轮的MOCs永久孔隙率的新策略,使其能够用作多相催化剂。在非配位溶剂、均三甲苯和对二甲苯中进行合成后溶剂热处理,有效地保留了溶剂抽空的MOCs的堆积结构,同时防止笼团聚。所得的MOCs表现出优异的氮吸附容量,具有高表面积(对于MOP-23,S = 1934 m²/g),这是多孔MOCs报道的最高值之一。有趣的是,虽然溶剂热处理将铜桨轮簇中的Cu(II)还原为Cu(I),但具有混合价态Cu(I)/Cu(II)的MOCs保持了它们的结晶度和永久孔隙率。这些MOCs的催化活性在铜(I)催化的水合酰胺合成中得到了成功检验,突出了MOCs作为通用反应平台的前景。