Twisted‐Planar Molecular Engineering with Sonication‐Induced J‐Aggregation to Design Near‐Infrared J‐Aggregates for Enhanced Phototherapy DOI
Yubo Liu,

Yuchen Song,

Zhong‐Hong Zhu

и другие.

Angewandte Chemie, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 11, 2024

Abstract J‐aggregates show great promise in phototherapy, but are limited to specific molecular skeletons and poor self‐assembly controllability. Herein, we report a twisted‐planar strategy with sonication‐induced J‐aggregation develop donor–acceptor (D–A) type for phototherapy. With propeller aggregation‐induced emission (AIE) moieties as the twisted subunits thiophene planar π‐bridge, optimal π‐interaction MTSIC induces appropriate slip angle formation, redshifting absorption from 624 nm 790 nm. In contrast, shorter π‐planarity results amorphous aggregates, elongation promotes charge transfer (CT) coupled J‐aggregates. Sonication was demonstrated be effective controlling behaviors of MTSIC, which enables transformation aggregates H‐intermediates, finally stable After encapsulation lipid‐PEG, resultant J‐dots enhanced phototherapeutic effects over dots, including brightness, reactive oxygen species (ROS) generation, photothermal conversion, delivering superior cancer phototherapy performance. This work not only advances D–A design also provides promising supramolecular assembly development.

Язык: Английский

The Second Near-Infrared (NIR-II) Window Excitable/Emissive Organic/Polymeric Fluorescent Molecules for Bioimaging Application DOI Creative Commons
Guannan Liu, Chenguang Wang, Geyu Lu

и другие.

Journal of Innovative Optical Health Sciences, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 15, 2024

The fluorescence imaging (FLI) in the second near-infrared window (NIR-II, 1000–1700[Formula: see text]nm) has attracted considerable attention past decade. In contrast to conventional NIR-I excitation (808[Formula: text]nm/980[Formula: text]nm), FLI with NIR-II (1064[Formula: text]nm/other wavelength beyond 1000[Formula: can afford deeper tissue penetration depth high clarity due merits of suppressed photon scattering and diminished autofluorescence. this review, we have summarized excitable/emissive organic/polymeric fluorophores recently developed. characteristics these such as chemical structures photophysical properties also been critically discussed. Furthermore, latest development noninvasive vivo was highlighted. ideal results emphasized importance enabling deep high-resolution imaging. Finally, a perspective on challenges prospects We expected review will be served source inspiration for researchers, stimulating creation novel excitable fostering bioimaging applications.

Язык: Английский

Процитировано

1

Side Chain Phenyl Isomerization‐Induced Spatial Conjugation for Achieving Efficient NIR‐II Phototheranostic Agents DOI Open Access

Chunbin Li,

Mengfan Yao,

Guoyu Jiang

и другие.

Angewandte Chemie, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 9, 2024

Abstract The contradiction of near‐infrared II (NIR‐II) emission and photothermal effects limits the development phototheranostic agents (PTAs) in many emerging cutting‐edge applications. Organic aggregates present a promising opportunity for balance competitive relaxation processes through manipulation molecular structure packing. Herein, side chain phenyl isomerization‐induced spatial conjugation was proposed constructing A‐D‐A type NIR‐II PTAs with simultaneous enhancement fluorescence brightness properties. Three pairs mutually isomeric fluorophores, whose phenyls respectively located at outside ( o ‐series) inside i chain, were designed synthesized. positional isomerization endows ‐series crystals strong between group on backbone, as well interlocked planar network, which is different to that observed ‐series. Thus, all nanoparticles (NPs) exhibit red‐shifted absorption, enhanced emission, superior properties than their counterparts. A prominent member ‐series, ‐ITNP NPs, demonstrated efficacy facilitating angiography, tumor localization, imaging‐guided therapy. success this strategy paves way precise control aggregation behavior further efficient PTAs.

Язык: Английский

Процитировано

0

Twisted‐Planar Molecular Engineering with Sonication‐Induced J‐Aggregation to Design Near‐Infrared J‐Aggregates for Enhanced Phototherapy DOI
Yubo Liu,

Yuchen Song,

Zhong‐Hong Zhu

и другие.

Angewandte Chemie, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 11, 2024

Abstract J‐aggregates show great promise in phototherapy, but are limited to specific molecular skeletons and poor self‐assembly controllability. Herein, we report a twisted‐planar strategy with sonication‐induced J‐aggregation develop donor–acceptor (D–A) type for phototherapy. With propeller aggregation‐induced emission (AIE) moieties as the twisted subunits thiophene planar π‐bridge, optimal π‐interaction MTSIC induces appropriate slip angle formation, redshifting absorption from 624 nm 790 nm. In contrast, shorter π‐planarity results amorphous aggregates, elongation promotes charge transfer (CT) coupled J‐aggregates. Sonication was demonstrated be effective controlling behaviors of MTSIC, which enables transformation aggregates H‐intermediates, finally stable After encapsulation lipid‐PEG, resultant J‐dots enhanced phototherapeutic effects over dots, including brightness, reactive oxygen species (ROS) generation, photothermal conversion, delivering superior cancer phototherapy performance. This work not only advances D–A design also provides promising supramolecular assembly development.

Язык: Английский

Процитировано

0