Direct and Linker-Exchange Alcohol-Assisted Hydrothermal Synthesis of Imide-Linked Covalent Organic Frameworks

被引:47
|
作者
Maschita, Johannes [1 ,2 ]
Banerjee, Tanmay [3 ]
Lotsch, Bettina, V [1 ,2 ,4 ,5 ]
机构
[1] Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany
[2] Univ Munich LMU, Dept Chem, D-81377 Munich, Germany
[3] BITS Pilani, Dept Chem, Pilani Campus, Pilani 333031, Rajasthan, India
[4] E Convers, D-80799 Munich, Germany
[5] Ctr Nanosci, D-80799 Munich, Germany
关键词
CRYSTALLINE; STRATEGY; WATER;
D O I
10.1021/acs.chemmater.1c04051
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Covalent organic frameworks (COFs) are an extensively studied class of porous materials, which distinguish themselves from other porous polymers in their crystallinity and high degree of modularity, enabling a wide range of applications. However, the established synthetic protocols for the synthesis of stable and crystalline COFs, such as imide-linked COFs, often requires the use of high boiling solvents and toxic catalysts, making their synthesis expensive and environmentally harmful. Herein, we report a new environmentally friendly strategy-an alcohol-assisted hydrothermal polymerization approach (aaHTP) for the synthesis of a wide range of crystalline and porous imide-linked COFs. This method allows us to gain access to new COFs and to avoid toxic solvents by up to 90% through substituting commonly used organic solvent mixtures with water and small amounts of n-alcohols without being restricted to water-soluble linker molecules. Additionally, we use the aaHTP to demonstrate an eco-friendly COF-to-COF transformation of an imine-linked COF into a novel imide-linked COF via linkage replacement, inaccessible using published reaction conditions.
引用
收藏
页码:2249 / 2258
页数:10
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