Construction of Function‐Oriented Core–Shell Nanostructures in Hydrogen‐Bonded Organic Frameworks for Near‐Infrared‐Responsive Bacterial Inhibition

Exploration of effective ways to integrate various functional species into hydrogen‐bonded organic frameworks (HOFs) is critically important for their applications but highly challenging. In this study, according to the “bottle‐around‐ship” strategy, core–shell heterostructure of upconversion nanopa...

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Published in:	Angewandte Chemie International Edition Vol. 60; no. 49; pp. 25701 - 25707
Main Authors:	Liu, Bai‐Tong, Pan, Xiao‐Hong, Zhang, Ding‐Yang, Wang, Rui, Chen, Jun‐Yu, Fang, Han‐Ru, Liu, Tian‐Fu
Format:	Journal Article
Language:	English
Published:	Germany Wiley Subscription Services, Inc 01.12.2021
Edition:	International ed. in English
Subjects:	Anti-Bacterial Agents - chemical synthesis Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology antimicrobials Composite materials Core-shell structure core–shell composite E coli Energy transfer Escherichia coli - drug effects Heterostructures Hydrogen Bonding I.R. radiation Imides - chemical synthesis Imides - chemistry Imides - pharmacology Infrared Rays Irradiation Microbial Sensitivity Tests Nanocomposites Nanoparticles Nanostructures - chemistry Near infrared radiation Particle Size Perylene - analogs & derivatives Perylene - chemical synthesis Perylene - chemistry Perylene - pharmacology photodynamic Photoresponse Photosensitizing Agents - chemical synthesis Photosensitizing Agents - chemistry Photosensitizing Agents - pharmacology photothermal Porosity resonance energy transfer Surface Properties photothermal resonance energy transfer antimicrobials photodynamic core-shell composite
ISSN:	1433-7851, 1521-3773, 1521-3773
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Abstract	Exploration of effective ways to integrate various functional species into hydrogen‐bonded organic frameworks (HOFs) is critically important for their applications but highly challenging. In this study, according to the “bottle‐around‐ship” strategy, core–shell heterostructure of upconversion nanoparticles (UCNPs) and HOFs was fabricated for the first time via a ligand‐grafting stepwise method. The UCNPs “core” can effectively upconvert near‐infrared (NIR) irradiation (980 nm) into visible light (540 nm and 653 nm), which further excites the perylenediimide‐based HOF “shell” through resonance energy transfer. In this way, the nanocomposite inherits the high porosity, excellent photothermal and photodynamic efficiency, NIR photoresponse from two parent materials, achieving intriguing NIR‐responsive bacterial inhibition toward Escherichia coli. This study may shed light on the design of functional HOF‐based composite materials, not only enriching the HOF library but also broadening the horizon of their potential applications. In this study, core–shell heterostructures of upconversion nanoparticles (UCNPs) and hydrogen‐bonded organic frameworks (HOFs) were fabricated via a stepwise ligand‐grafting method. The UCNP “core” can effectively upconvert near‐infrared (NIR) irradiation into visible ranges, which can further excite the HOF “shell” to achieve near‐infrared‐responsive photothermal and photodynamic bacterial inhibition.
AbstractList	Exploration of effective ways to integrate various functional species into hydrogen‐bonded organic frameworks (HOFs) is critically important for their applications but highly challenging. In this study, according to the “bottle‐around‐ship” strategy, core–shell heterostructure of upconversion nanoparticles (UCNPs) and HOFs was fabricated for the first time via a ligand‐grafting stepwise method. The UCNPs “core” can effectively upconvert near‐infrared (NIR) irradiation (980 nm) into visible light (540 nm and 653 nm), which further excites the perylenediimide‐based HOF “shell” through resonance energy transfer. In this way, the nanocomposite inherits the high porosity, excellent photothermal and photodynamic efficiency, NIR photoresponse from two parent materials, achieving intriguing NIR‐responsive bacterial inhibition toward Escherichia coli. This study may shed light on the design of functional HOF‐based composite materials, not only enriching the HOF library but also broadening the horizon of their potential applications. Exploration of effective ways to integrate various functional species into hydrogen‐bonded organic frameworks (HOFs) is critically important for their applications but highly challenging. In this study, according to the “bottle‐around‐ship” strategy, core–shell heterostructure of upconversion nanoparticles (UCNPs) and HOFs was fabricated for the first time via a ligand‐grafting stepwise method. The UCNPs “core” can effectively upconvert near‐infrared (NIR) irradiation (980 nm) into visible light (540 nm and 653 nm), which further excites the perylenediimide‐based HOF “shell” through resonance energy transfer. In this way, the nanocomposite inherits the high porosity, excellent photothermal and photodynamic efficiency, NIR photoresponse from two parent materials, achieving intriguing NIR‐responsive bacterial inhibition toward Escherichia coli . This study may shed light on the design of functional HOF‐based composite materials, not only enriching the HOF library but also broadening the horizon of their potential applications. Exploration of effective ways to integrate various functional species into hydrogen‐bonded organic frameworks (HOFs) is critically important for their applications but highly challenging. In this study, according to the “bottle‐around‐ship” strategy, core–shell heterostructure of upconversion nanoparticles (UCNPs) and HOFs was fabricated for the first time via a ligand‐grafting stepwise method. The UCNPs “core” can effectively upconvert near‐infrared (NIR) irradiation (980 nm) into visible light (540 nm and 653 nm), which further excites the perylenediimide‐based HOF “shell” through resonance energy transfer. In this way, the nanocomposite inherits the high porosity, excellent photothermal and photodynamic efficiency, NIR photoresponse from two parent materials, achieving intriguing NIR‐responsive bacterial inhibition toward Escherichia coli. This study may shed light on the design of functional HOF‐based composite materials, not only enriching the HOF library but also broadening the horizon of their potential applications. In this study, core–shell heterostructures of upconversion nanoparticles (UCNPs) and hydrogen‐bonded organic frameworks (HOFs) were fabricated via a stepwise ligand‐grafting method. The UCNP “core” can effectively upconvert near‐infrared (NIR) irradiation into visible ranges, which can further excite the HOF “shell” to achieve near‐infrared‐responsive photothermal and photodynamic bacterial inhibition. Exploration of effective ways to integrate various functional species into hydrogen-bonded organic frameworks (HOFs) is critically important for their applications but highly challenging. In this study, according to the "bottle-around-ship" strategy, core-shell heterostructure of upconversion nanoparticles (UCNPs) and HOFs was fabricated for the first time via a ligand-grafting stepwise method. The UCNPs "core" can effectively upconvert near-infrared (NIR) irradiation (980 nm) into visible light (540 nm and 653 nm), which further excites the perylenediimide-based HOF "shell" through resonance energy transfer. In this way, the nanocomposite inherits the high porosity, excellent photothermal and photodynamic efficiency, NIR photoresponse from two parent materials, achieving intriguing NIR-responsive bacterial inhibition toward Escherichia coli. This study may shed light on the design of functional HOF-based composite materials, not only enriching the HOF library but also broadening the horizon of their potential applications.Exploration of effective ways to integrate various functional species into hydrogen-bonded organic frameworks (HOFs) is critically important for their applications but highly challenging. In this study, according to the "bottle-around-ship" strategy, core-shell heterostructure of upconversion nanoparticles (UCNPs) and HOFs was fabricated for the first time via a ligand-grafting stepwise method. The UCNPs "core" can effectively upconvert near-infrared (NIR) irradiation (980 nm) into visible light (540 nm and 653 nm), which further excites the perylenediimide-based HOF "shell" through resonance energy transfer. In this way, the nanocomposite inherits the high porosity, excellent photothermal and photodynamic efficiency, NIR photoresponse from two parent materials, achieving intriguing NIR-responsive bacterial inhibition toward Escherichia coli. This study may shed light on the design of functional HOF-based composite materials, not only enriching the HOF library but also broadening the horizon of their potential applications.
Author	Liu, Bai‐Tong Pan, Xiao‐Hong Liu, Tian‐Fu Fang, Han‐Ru Chen, Jun‐Yu Zhang, Ding‐Yang Wang, Rui
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Snippet	Exploration of effective ways to integrate various functional species into hydrogen‐bonded organic frameworks (HOFs) is critically important for their... Exploration of effective ways to integrate various functional species into hydrogen-bonded organic frameworks (HOFs) is critically important for their...
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SubjectTerms	Anti-Bacterial Agents - chemical synthesis Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology antimicrobials Composite materials Core-shell structure core–shell composite E coli Energy transfer Escherichia coli - drug effects Heterostructures Hydrogen Bonding I.R. radiation Imides - chemical synthesis Imides - chemistry Imides - pharmacology Infrared Rays Irradiation Microbial Sensitivity Tests Nanocomposites Nanoparticles Nanostructures - chemistry Near infrared radiation Particle Size Perylene - analogs & derivatives Perylene - chemical synthesis Perylene - chemistry Perylene - pharmacology photodynamic Photoresponse Photosensitizing Agents - chemical synthesis Photosensitizing Agents - chemistry Photosensitizing Agents - pharmacology photothermal Porosity resonance energy transfer Surface Properties
Title	Construction of Function‐Oriented Core–Shell Nanostructures in Hydrogen‐Bonded Organic Frameworks for Near‐Infrared‐Responsive Bacterial Inhibition
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