posted on 2023-11-08, 21:40authored byXin Tao, Zhen Wang, Qing-Pu Zhang, Ningning Liu, Yu-Ling Sun, Ruo-Xin Niu, Ruixue Sun, Xiaoyan Wang, Bien Tan, Chun Zhang
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(N-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.