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使用液滴纳米反应器连续一锅法合成纳米金属有机框架及其后合成修饰

Continuous, One-pot Synthesis and Post-Synthetic Modification of NanoMOFs Using Droplet Nanoreactors.

作者信息

Jambovane Sachin R, Nune Satish K, Kelly Ryan T, McGrail B Peter, Wang Zheming, Nandasiri Manjula I, Katipamula Shanta, Trader Cameron, Schaef Herbert T

机构信息

Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99354, United States.

Energy and Environment Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States.

出版信息

Sci Rep. 2016 Nov 8;6:36657. doi: 10.1038/srep36657.

Abstract

Metal-organic frameworks (MOFs); also known as porous coordination polymers (PCP) are a class of porous crystalline materials constructed by connecting metal clusters via organic linkers. The possibility of functionalization leads to virtually infinite MOF designs using generic modular methods. Functionalized MOFs can exhibit interesting physical and chemical properties including accelerated adsorption kinetics and catalysis. Although there are discrete methods to synthesize well-defined nanoscale MOFs, rapid and flexible methods are not available for continuous, one-pot synthesis and post-synthetic modification (functionalization) of MOFs. Here, we show a continuous, scalable nanodroplet-based microfluidic route that not only facilitates the synthesis of MOFs at a nanoscale, but also offers flexibility for direct functionalization with desired functional groups (e.g., -COCH, fluorescein isothiocyanate; FITC). In addition, the presented route of continuous manufacturing of functionalized nanosized MOFs takes significantly less time compared to state-of-the-art batch methods currently available (1 hr vs. several days). We envisage our approach to be a breakthrough method for synthesizing complex functionalized nanomaterials (metal, metal oxides, quantum dots and MOFs) that are not accessible by direct batch processing and expand the range of a new class of functionalized MOF-based functional nanomaterials.

摘要

金属有机框架材料(MOFs);也被称为多孔配位聚合物(PCP),是一类通过有机连接体连接金属簇构建而成的多孔晶体材料。功能化的可能性使得使用通用模块化方法几乎能实现无限的MOF设计。功能化的MOFs可展现出有趣的物理和化学性质,包括加速的吸附动力学和催化作用。尽管存在合成定义明确的纳米级MOFs的离散方法,但对于MOFs的连续一锅法合成和合成后修饰(功能化),尚无快速且灵活的方法。在此,我们展示了一种基于连续、可扩展的纳米液滴的微流控路线,该路线不仅有助于在纳米尺度上合成MOFs,还为用所需官能团(如 -COCH、异硫氰酸荧光素;FITC)进行直接功能化提供了灵活性。此外,与目前可用的最先进的分批方法相比,所展示的功能化纳米级MOFs的连续制造路线所需时间显著减少(1小时对比数天)。我们设想我们的方法是合成复杂功能化纳米材料(金属、金属氧化物、量子点和MOFs)的一种突破性方法,这些材料无法通过直接分批处理获得,并扩展了一类新型基于功能化MOF的功能纳米材料的范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2faa/5099625/a209341e1b73/srep36657-f1.jpg

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