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共价有机框架的管状自组装。

Microtubular Self-Assembly of Covalent Organic Frameworks.

机构信息

Universität Würzburg, Institut für Organische Chemie, Am Hubland, 97074, Würzburg, Germany.

Center for Nanosystems Chemistry &, Bavarian Polymer Institute, BPI, Theodor-Boveri-Weg, 97074, Würzburg, Germany.

出版信息

Angew Chem Int Ed Engl. 2018 Jan 15;57(3):846-850. doi: 10.1002/anie.201708526. Epub 2017 Dec 13.

Abstract

Despite significant progress in the synthesis of covalent organic frameworks (COFs), reports on the precise construction of template-free nano- and microstructures of such materials have been rare. In the quest for dye-containing porous materials, a novel conjugated framework DPP-TAPP-COF with an enhanced absorption capability up to λ=800 nm has been synthesized by utilizing reversible imine condensations between 5,10,15,20-tetrakis(4-aminophenyl)porphyrin (TAPP) and a diketopyrrolopyrrole (DPP) dialdehyde derivative. Surprisingly, the obtained COF exhibited spontaneous aggregation into hollow microtubular assemblies with outer and inner tube diameters of around 300 and 90 nm, respectively. A detailed mechanistic investigation revealed the time-dependent transformation of initial sheet-like agglomerates into the tubular microstructures.

摘要

尽管在共价有机框架(COFs)的合成方面取得了重大进展,但关于此类材料的无模板纳米和微观结构的精确构建的报道却很少。在寻求含染料的多孔材料的过程中,通过利用 5,10,15,20-四(4-氨基苯基)卟啉(TAPP)和二酮吡咯并吡咯(DPP)二醛衍生物之间的可逆亚胺缩合反应,合成了具有增强的吸收能力,达到 λ=800nm 的新型共轭框架 DPP-TAPP-COF。令人惊讶的是,所得到的 COF 自发聚集为具有约 300nm 和 90nm 内外管直径的空心管状组装体。详细的机理研究揭示了初始片状聚集体向管状微观结构的时间依赖性转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/067f/6519380/85c016189a53/ANIE-57-846-g001.jpg

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