Nanohydrogelation of covalent organic frameworks (COFs) will undoubtedly open up new applications for them in water, such as aqueous catalysis and biomedicine. It is currently a great challenge to achieve water dispersion of COFs through either bottom-up construction strategies or top-down exfoliating technologies. Herein, poly(-isopropylacrylamide) (PNIPAM)-postmodified COF nanohydrogels (COF-NHGs) are successfully designed and synthesized via in situ atom-transfer radical polymerization (ATRP) on a scaffold of COFs. During the polymer growth process, the bulk COFs are exfoliated into nanosheets with a lateral size of ∼500 nm and a thickness of ∼6.5 nm. Moreover, their size can be precisely controlled by the degree of polymerization of PNIPAMs. In aqueous solution, the obtained COF-NHGs are assembled into nanohydrogels retaining intra-plane crystallinity and exhibit a temperature-sensitive sol-gel phase transition. With excellent solubility in organic solvents, the COF-NHGs' intrinsic physical properties in the solution state can be characterized through their solution nuclear magnetic resonance and ultraviolet absorption spectra. These results put forward new opportunities for regulating the solution processability of COFs and building an intelligent, stimuli-response platform of COF-polymer composite nanohydrogels for device applications.
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http://dx.doi.org/10.1021/jacs.3c10296 | DOI Listing |
Chem Sci
December 2024
College of Chemistry and Pharmaceutical Engineering, Nanyang Normal University Nanyang 473601 P. R. China
The conversion of carbon dioxide (CO) into carbon-neutral fuels using solar energy is crucial for achieving energy sustainability. However, the high carrier charge recombination and low CO adsorption capacity of the photocatalysts present significant challenges. In this paper, a TAPB-COF@ZnInS-30 (TAPB-COFZ-30) heterojunction photocatalyst was constructed by growth of ZnInS (ZIS) on a hollow covalent organic framework (HCOF) with a hollow core-shell structure for CO to CO conversion.
View Article and Find Full Text PDFChem Asian J
January 2025
University of Kerala, Department of Chemistry, Kariavattom Campus, 695581, Thiruvananthapuram, INDIA.
Crystallinity, stability, and complexity are significant factors to consider in the design and development of covalent organic frameworks (COFs). Among various building blocks used, 1,3,5-triformylphloroglucinol (Tp) is notable for enhancing both crystallinity and structural stability in COFs. Tp facilitates the formation of β-ketoenamine-linked COFs through keto-enol tautomerism when reacted with aromatic amines.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
College of Chemistry, Sichuan University, Chengdu 610064, China.
The adsorption of radioactive iodine is a critical concern in nuclear safety and environmental protection due to its hazardous nature and long half-life. Covalent organic frameworks (COFs) have emerged as promising materials for capturing radioactive iodine owing to their tunable porosity, high surface area, and versatile functionalization capabilities. This review provides a comprehensive overview of the application of COFs in the adsorption of radioactive iodine.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Shandong Normal University, Jinan 250014, P. R. China.
Herein, we report a nanoscale composite COF material loaded with copper peroxide (CuO) and nitric oxide (NO) prodrug a stepwise post-synthetic modification. The obtained CuO2@COF-SNO can undergo a cascade reaction in the tumor microenvironment to generate reactive oxygen and nitrogen species (ROS/RNS) to enhance chemodynamic therapy of the tumor.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing 100190, PR China.
The efficient removal of organic contaminants from high-salinity wastewater is crucial for resource recovery and achieving zero discharge. Nanofiltration (NF) membranes are effective in separating organic compounds and monovalent salts, but they typically exhibit an excessive rejection of divalent salts. Modifying the charge characteristics of NF membranes can improve salt permeation; however, the role of charge spatial distribution in governing salt transport behavior is not fully understood.
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