Kim Yeonghun, Lee Sanghyeop, Chen Ying-Pin, Lee Byeongchan, Lee Sunggi, Park Jinhee
Department of Physics and Chemistry, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Republic of Korea.
Electrode Engineering, Panasonic Energy of North America, Reno, NV, 89502, USA.
Small. 2024 Mar;20(9):e2305999. doi: 10.1002/smll.202305999. Epub 2023 Oct 15.
An unprecedented correlation between the catalytic activity of a Zr-based UiO-type metal-organic framework (MOF) and its degree of interpenetration (DOI) is reported. The DOI of an MOF is hard to control owing to the high-energy penalty required to construct a partially interpenetrated structure. Surprisingly, strong interactions between building blocks (inter-ligand hydrogen bonding) facilitate the formation of partially interpenetrated structures under carefully regulated synthesis conditions. Moreover, catalytic conversion rates for cyanosilylation and Knoevenagel condensation reactions are found to be proportional to the DOI of the MOF. Among MOFs with DOIs in the 0-100% range, that with a DOI of 87% is the most catalytically active. Framework interpenetration is known to lower catalytic performance by impeding reactant diffusion. A higher effective reactant concentration due to tight inclusion in the interpenetrated region is possibly responsible for this inverted result.
据报道,一种基于锆的UiO型金属有机框架(MOF)的催化活性与其互穿程度(DOI)之间存在前所未有的相关性。由于构建部分互穿结构需要高昂的能量代价,MOF的DOI很难控制。令人惊讶的是,在精心调控的合成条件下,构建单元之间的强相互作用(配体间氢键)有助于形成部分互穿结构。此外,发现氰基硅烷化反应和Knoevenagel缩合反应的催化转化率与MOF的DOI成正比。在DOI为0-100%范围内的MOF中,DOI为87%的MOF催化活性最高。众所周知,框架互穿会通过阻碍反应物扩散而降低催化性能。互穿区域内紧密包合导致的较高有效反应物浓度可能是造成这种相反结果的原因。