机械合成
机械化学
网状结缔组织
催化作用
氢键
材料科学
基质(化学分析)
纳米技术
化学
化学工程
分子
复合材料
有机化学
球磨机
病理
工程类
医学
作者
Wei‐Kang Qin,Duan–Hui Si,Qi Yin,Gao X,Qianqian Huang,Ya‐Nan Feng,Lei Xie,Shuo Zhang,Xinsong Huang,Tian‐Fu Liu,Rong Cao
标识
DOI:10.1002/anie.202202089
摘要
Rational synthesis of hydrogen-bonded organic frameworks (HOFs) with predicted structure has been a long-term challenge. Herein, by using the efficient, simple, low-cost, and scalable mechanosynthesis, we demonstrate that reticular chemistry is applicable to HOF assemblies based on building blocks with different geometry, connectivity, and functionality. The obtained crystalline HOFs show uniform nano-sized morphology, which is challenging or unachievable for conventional solution-based methods. Furthermore, the one-pot mechanosynthesis generated a series of Pd@HOF composites with noticeably different CO oxidation activities. In situ DRIFTS studies indicate that the most efficient composite, counterintuitively, shows the weakest CO affinity to Pd sites while the strongest CO affinity to HOF matrix, revealing the vital role of porous matrix to the catalytic performance. This work paves a new avenue for rational synthesis of HOF and HOF-based composites for broad application potential.
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