反离子
化学
激发
荧光
多路复用
材料科学
聚集诱导发射
分析化学(期刊)
光学
离子
计算机科学
色谱法
物理
电信
有机化学
量子力学
作者
Yang Yang,Caixia Sun,Shangfeng Wang,Kui Yan,Mengyao Zhao,Bin Wu,Fan Zhang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2022-03-16
卷期号:61 (24): e202117436-e202117436
被引量:119
标识
DOI:10.1002/anie.202117436
摘要
Photon excitation and emission at the NIR-II spectral window enable high-contrast deep-tissue bioimaging. However, multiplexed imaging with NIR-II excitation and emission has been hampered by the limited chemical strategies to develop bright fluorophores with tunable absorption in this spectral regime. Herein, we developed a series of heptamethine cyanines (HCs) with varied absorption/emission maxima spanning from 1100 to 1600 nm through a physical organic approach. A bulky counterion paired to HCs was found to elicit substantial improvements in absorptivity (7-fold), brightness (14-fold), and spectral profiles in water, addressing a notorious quenching problem of NIR-II cyanines due to aggregation and polarization. We demonstrated the utilities of HC1222 and HC1342 for high-contrast dual-color imaging of circulatory system, lymphatic structures, tumor, and organ function in living mice under 1120 nm and 1319 nm excitation, showing HCs as a promising platform for non-invasive bioimaging.
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