Synthesis of Side-Chain-Free Hydrazone-Linked Covalent Organic Frameworks through Supercritical Carbon Dioxide Activation

Shashini D. Diwakara, G. McCandless, Sampath B. Alahakoon, Ronald A. Smaldone
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引用次数: 3

Abstract

Abstract Supercritical carbon dioxide (scCO2) activation provides milder conditions to process covalent organic frameworks (COFs) without compromising their crystallinity and porosity. To this end, three hydrazone COFs (TFPB-DHz COF, TFPT-DHz COF, Py-DHz COF) were synthesized with a terephthaloyl dihydrazide linker (DHz) which has no substituents. To date, the synthesis of hydrazone COFs without a narrow range of alkoxy linkers has not been possible. The scCO2-activated hydrazone-linked COFs in this study were crystalline and had high surface areas (surface areas of TFPB-DHz COF, TFPT-DHz COF, and Py-DHz COF were 790, 1199, and 932 m2/g, respectively). This study shows the significance of using milder activation methods for making hydrazone-linked COF structures that were previously inaccessible.
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超临界二氧化碳活化法合成无侧链腙连接共价有机骨架
超临界二氧化碳(scCO2)活化为处理共价有机框架(COFs)提供了更温和的条件,而不会影响它们的结晶度和孔隙度。为此,以不含取代基的对苯二甲酰二肼连接剂(DHz)合成了三种腙COFs (TFPB-DHz COF、TFPT-DHz COF、Py-DHz COF)。迄今为止,没有窄范围烷氧基连接的腙COFs的合成是不可能的。本研究中scco2活化的腙连接的COFs呈结晶状,具有高表面积(TFPB-DHz COF、TFPT-DHz COF和Py-DHz COF的表面积分别为790、1199和932 m2/g)。这项研究表明,使用温和的活化方法来制造以前无法获得的腙连接COF结构具有重要意义。
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CiteScore
3.70
自引率
0.00%
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审稿时长
12 weeks
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