Microdroplet-Enabled Interfacial Electron Transfer Accelerates Schiff Base Condensation for Ultrafast Covalent Organic Framework Synthesis
Imine-linked covalent organic frameworks (COFs) are attractive crystalline porous materials, yet their synthesis is kinetically limited by sluggish acid-catalyzed Schiff base condensation. Here we report a microdroplet-driven strategy that enables rapid and scalable COF formation via an unconventional interfacial pathway. Continuous ultrasonic nebulization of aqueous monomers affords crystalline imine-linked COFs within minutes at room temperature, without catalysts or organic solvents, achieving reaction rates orders of magnitude higher than batch synthesis. Mechanistic studies reveal the gas-liquid interface of microdroplets as an electronically active reaction zone, where interfacial electron transfer generates radical and anionic nitrogen species that trigger a nonclassical condensation mechanism. Interfacial enrichment, hydrogen-bond symmetry breaking, and strong electric fields cooperatively lower activation barriers and promote dehydration-driven framework growth. This general and scalable platform transforms the air-water interface into an active electronic reactor, establishing a new paradigm for framework synthesis and interfacial reaction acceleration.
Authors
- Junju Mu (ORCID: https://orcid.org/0000-0002-7382-2182)
- Feng Wang (ORCID: https://orcid.org/0000-0002-9167-8743)
- Peng Jin (ORCID: https://orcid.org/0000-0001-6137-6659)
- Xuke Chen
- Xukai Zhou (ORCID: https://orcid.org/0000-0003-0053-5075)
- Zilun Yu
- Jianhan Wu
- Zhendong Luo
- Sihui Meng
Institutions
- Dalian Institute of Chemical Physics (CN)
- Chinese Academy of Sciences (CN)
- Institute of Catalysis and Petrochemistry (RU)
- University of Chinese Academy of Sciences (CN)
- State Key Laboratory of Catalysis
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-06-17
- DOI
- https://doi.org/10.1021/jacs.6c03031
- Primary Topic
- Covalent Organic Framework Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00