Source abstract
Abstract
Abstract Through synthetic chemistry, the development of molecular devices for the precise selective recognition and active transport of small molecules stands as one of the most ambitious objectives in extensive medical, environmental, and biological applications. The periodical channels of the metal–organic frameworks (MOFs) with excellent chemical affinity offer vast regulatory space for reaching this goal. Herein, by post‐modifying fluorescent probes and ionic liquid molecules into the Zr‐MOFs (NU‐1000), a donor–acceptor (D‐A) system within the periodical 1D channels is created to construct a hydrodynamic fluidic pump within the abundant 1D channels. Irradiation with light serves to initiate and direct fluid motion, expediting the transport of H 2 O 2 molecules to the active site, thus boosting the sensor sensitivity through gas enrichment. The rapid mass transfer, characterized by a high flow rate and intensified interaction between the D‐A system and H 2 O 2 molecules, enables the detection of H 2 O 2 at concentrations as low as 20 ppb. Besides, with the aid of incident light, the pump system exhibits active transport characteristics by transporting radicals derived from H 2 O 2 against a concentration gradient, reaching a remarkable 10 th cycle. The strategy of achieving active transport of small molecules through pore modification holds promise for advancing the development of artificial bioactive channels.
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Affiliations
Key Laboratory of Colloid and Interface Chemistry Ministry of Education Shandong University Jinan 250100 China
Qilu University of Technology (Shandong Academy of Sciences) Shandong Analysis and Test Center Jinan 250014 China
State Key Laboratory of Biochemical Engineering Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 China
Funding
Natural Science Foundation of Beijing Municipality · Natural Science Foundation of Shandong Province · Taishan Scholar Foundation of Shandong Province · National Natural Science Foundation of China