Because of their good performance in diffusion‐limited processes, ordered macro‐microporous single‐crystalline metal‐organic frameworks (MOFs) have potential for use in various fields. However, there are still very few reports of the synthesis of such MOFs. A general synthesis methodology for ordered macro‐microporous single‐crystalline MOFs is highly desired. Here, a novel strategy is reported for synthesizing single‐crystalline ordered macro‐microporous MOFs by monodentate‐ligand‐induced in situ crystallization within a 3D ordered hard template in a double‐solvent system. A space‐confined growth model is proposed to clarify the shaping effect of the template; the role of the monodentate ligand is also analyzed. Moreover, a carbon material derived from the macro‐microporous MOF inherits the ordered interconnected macroporous structure. The improved diffusion and lower resistance, as well as the structural robustness, endow the derivative carbon material with superior rate performance and excellent cycling stability when prepared as electrodes for a supercapacitor. It is anticipated that the method will provide new paths to the synthesis of such macro‐microporous materials for applications in energy‐related fields and beyond.

Toxic solvents and catalysts, tedious monomer synthesis, as well as long reaction time significantly limit the sustainable and large-scale preparation and practical application of microporous polyimides (MPIs). In this work,...

In this study, a green and atom economical strategy has been developed to construct polybismaleimide-based microporous organic polymers (BMOPs).

In this work, a new type of hyper-crosslinked phosphate-based polymer (HCPP) polymerized by bis­(2-methacryloxyethyl)­phosphate has been developed for uranium and rare earth element (REE) extraction in an aqueous solution. The influence of the pH value, contact time, initial concentration, temperature, and competing ions on uranium adsorption of HCPP is investigated in detail. HCPP exhibits a maximum uranium adsorption capacity of up to 800 mg g–1 at pH = 6.0 and excellent selectivity toward uranium adsorption over coexisting ions, because of the high affinity between HCPP and uranium ions and dense phosphate groups on the backbone. It also demonstrates high adsorption performance in both simulated seawater with a high salt concentration and a real nuclear industrial effluent. Besides, the crosslinked network structure of HCPP endows this polymer with high chemical stability and reusability. Furthermore, the adsorption mechanism is probed by energy-dispersive spectroscopy, X-ray photoelectron spectroscopy, and Fourier transform infrared measurements. It is confirmed that the adsorption of uranium on the adsorbent originates from the interaction between phosphate groups and uranium ions. Meanwhile, HCPP also displays high REE adsorption capacities. This work indicates that the phosphate-based HCPP could be utilized as a promising adsorbent for the effective removal of uranium and REEs from aqueous solution.