Li Conger, Liu Junhong, Zhang Kexin, Zhang Songwei, Lee Yongjin, Li Tao
School of Physical Science and Technology, Shanghai Tech University, Shanghai, 201210, P. R. China.
Department of Chemical Engineering, Inha University, Incheon, 22212, Republic of Korea.
Angew Chem Int Ed Engl. 2021 Jun 14;60(25):14138-14145. doi: 10.1002/anie.202104487. Epub 2021 May 14.
This work describes the first generalizable method to modify various metal-organic framework (MOF) surfaces with polyimide, polysulfone, polycarbonate, and polymer of intrinsic microporosity-1 (PIM-1). The method first utilizes electrostatic adsorption to rapidly decorate positively charged MOF surfaces with a layer of negatively charged metal-organic nanocapsule, PgC Cu. After mixing with the polymer, the copper open metal sites on PgC Cu can coordinatively crosslink the polar functional groups on the surface polymer upon thermal activation thereby resulting in the immobilization of a uniform sub-10 nm polymer coating. We quantitatively analyzed the distribution of free path spacing between MOF particles and demonstrated that when the surface polymer matches the matrix polymer, the MOF dispersion was not only visually improved but also found to align perfectly with a theoretically predicted ideal dispersion model where no aggregation driving force was present.
这项工作描述了第一种可推广的方法,用于用聚酰亚胺、聚砜、聚碳酸酯和固有微孔聚合物-1(PIM-1)修饰各种金属有机框架(MOF)表面。该方法首先利用静电吸附,用一层带负电荷的金属有机纳米胶囊PgC Cu快速修饰带正电荷的MOF表面。与聚合物混合后,PgC Cu上的铜开放金属位点在热活化时可以与表面聚合物上的极性官能团配位交联,从而形成均匀的亚10纳米聚合物涂层。我们定量分析了MOF颗粒之间自由程间距的分布,并证明当表面聚合物与基体聚合物匹配时,MOF分散体不仅在视觉上得到改善,而且发现与理论预测的理想分散模型完美吻合,在该模型中不存在聚集驱动力。