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首页> 外文期刊>ACS applied materials & interfaces >Second Near-Infrared Aggregation-Induced Emission Fluorophores with Phenothiazine Derivatives as the Donor and 6,7-Diphenyl-[1,2,5]Thiadiazolo[3,4-g]Quinoxaline as the Acceptor for In Vivo Imaging
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Second Near-Infrared Aggregation-Induced Emission Fluorophores with Phenothiazine Derivatives as the Donor and 6,7-Diphenyl-[1,2,5]Thiadiazolo[3,4-g]Quinoxaline as the Acceptor for In Vivo Imaging

机译:第二近红外聚集诱导的发射荧光团,其具有吩噻嗪衍生物作为供体和6,7-二苯基 - [1,2,5]噻二唑[3,4 -g]喹喔啉作为体内成像的受体

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摘要

Traditional organic fluorophores generally have hydrophobic conjugated backbones and exhibit an aggregation-caused quenching emission property, which limits greatly their applications in the biological field. Aggregation-induced emission (ME) fluorophores can breakthrough this shortcoming and are more promising in biological imaging. In this paper, we synthesized three novel donor-acceptor-donor-type second near-infrared (NIR-II) fluorophores and studied their geometric and electronic structures and photophysical properties by both theoretical and experimental studies. All the three fluorophores had typical AIE characteristics, and their emission wavelength spanned the traditional near-infrared and NIR-II regions. They exhibited much stronger fluorescence after being encapsulated in polymer nanoparticles (NPs) than in solutions, and the fluorophore-loaded NPs had desirable biosafety and significant tumor accumulation, indicating that they have great application potentials in tumor detection.
机译:传统的有机荧光团通常具有疏水性共轭骨架,并且具有引起的引起的淬火发射性能,这极大地限制了它们在生物领域的应用。聚集诱导的发射(ME)荧光团可以突破这种缺点,并且在生物成像中更有前景。在本文中,我们合成了三种新型供体 - 供体型第二近红外(NIR-II)荧光团,并通过理论和实验研究研究了它们的几何和电子结构和光物理性质。所有三个荧光团都具有典型的AIE特性,并且它们的排放波长跨越传统的近红外和尼河II区。它们在将聚合物纳米颗粒(NPS)中封装之后呈现更强烈的荧光,并且荧光团的NPS具有理想的生物安全和显着的肿瘤积累,表明它们具有巨大的肿瘤检测潜力。

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