环加成
羧酸盐
炔烃
化学
双功能
催化作用
组合化学
3D打印
分子
胺气处理
材料科学
高分子化学
有机化学
复合材料
作者
J. Sebastián Manzano,Zachary B. Weinstein,Aaron D. Sadow,Igor I. Slowing
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2017-09-22
卷期号:7 (11): 7567-7577
被引量:61
标识
DOI:10.1021/acscatal.7b02111
摘要
3D printing of materials with active functional groups can provide custom-designed structures that promote chemical conversions. Catalytically active architectures were produced by photopolymerizing bifunctional molecules using a commercial stereolithographic 3D printer. Functionalities in the monomers included a polymerizable vinyl group to assemble the 3D structures and a secondary group to provide them with active sites. The 3D-printed architectures containing accessible carboxylic acid, amine, and copper carboxylate functionalities were catalytically active for the Mannich, aldol, and Huisgen cycloaddition reactions, respectively. The functional groups in the 3D-printed structures were also amenable to post-printing chemical modification. And as proof of principle, chemically active cuvette adaptors were 3D printed and used to measure in situ the kinetics of a heterogeneously catalyzed Mannich reaction in a conventional solution spectrophotometer. In addition, 3D-printed millifluidic devices with catalytically active copper carboxylate complexes were used to promote azide-alkyne cycloaddition under flow conditions. The importance of controlling the 3D architecture of the millifluidic devices was evidenced by enhancing reaction conversion upon increasing the complexity of the 3D prints.
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