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N−苯基萘酰亚胺聚集诱导发光分子用于细胞成像

黄文灵 蒋娜 朱颖 黄婉玲 瞿祎

黄文灵, 蒋娜, 朱颖, 黄婉玲, 瞿祎. N−苯基萘酰亚胺聚集诱导发光分子用于细胞成像[J]. 上海工程技术大学学报, 2022, 36(3): 301-308. doi: 10.12299/jsues.21-0237
引用本文: 黄文灵, 蒋娜, 朱颖, 黄婉玲, 瞿祎. N−苯基萘酰亚胺聚集诱导发光分子用于细胞成像[J]. 上海工程技术大学学报, 2022, 36(3): 301-308. doi: 10.12299/jsues.21-0237
HUANG Wenling, JIANG Na, ZHU Ying, HUANG Wanling, QU Yi. A N-phenylnaphthalimide derivative with aggregation-induced emission for cell imaging[J]. Journal of Shanghai University of Engineering Science, 2022, 36(3): 301-308. doi: 10.12299/jsues.21-0237
Citation: HUANG Wenling, JIANG Na, ZHU Ying, HUANG Wanling, QU Yi. A N-phenylnaphthalimide derivative with aggregation-induced emission for cell imaging[J]. Journal of Shanghai University of Engineering Science, 2022, 36(3): 301-308. doi: 10.12299/jsues.21-0237

N−苯基萘酰亚胺聚集诱导发光分子用于细胞成像

doi: 10.12299/jsues.21-0237
详细信息
    作者简介:

    黄文灵(2000−),女,在读硕士,研究方向为有机光电功能材料. E-mail:1216926181@qq.com

    通讯作者:

    瞿 祎(1984−),男,副教授,博士,研究方向为有机光电功能材料. E-mail:yiqu@sues.edu.cn

  • 中图分类号: O 652.7

A N-phenylnaphthalimide derivative with aggregation-induced emission for cell imaging

  • 摘要:

    聚集诱导发光分子在有机光电功能材料领域有着重要的应用价值. 利用常见的ACQ−活性萘酰亚胺染料, 通过典型的铃木偶联反应,在萘酰亚胺荧光团的4位引入一个去平面化苯环,设计并合成两个新的聚集诱导发光(Aggregation-Induced Emission, AIE)分子NIRF2和NIRF6. 通过1H、13C NMR和HRMS谱对其进行结构表征. 通过紫外−可见光谱、荧光发射光谱和动态激光散射测试研究二者结构与聚集诱导发光的构效关系. 最后,NIRF2和NIRF6成功应用于Hela细胞的细胞质成像. 研究表明,提出的优化设计策略可以实现萘酰亚胺基AIE活性分子的构建.

  • 图  1  化合物NIRF2和NIRF6的结构

    Figure  1.  Structures of compounds NIRF2 and NIRF6

    图  2  化合物NIRF2和NIRF6的合成路线

    Figure  2.  Synthesis routine of compounds NIRF2 and NIRF6.

    图  3  不同有机溶剂中化合物NIRF2和NIRF6的紫外−可见光谱和荧光发射光谱

    Figure  3.  UV-vis and fluorescence emission spectra of NIRF2 and NIRF6 in different solvents

    图  4  化合物NIRF2和NIRF6在四氢呋喃−水混合体系中的聚集诱导发光性质

    Figure  4.  Aggregation-induced emission properties of compounds NIRF2 and NIRF6 in the THF-water mixture

    图  5  化合物NIRF6在不同聚集态下的动力学光散射结果

    Figure  5.  Dynamic light scattering results of compound NIRF6 in different aggregation states

    图  6  化合物NIRF2和NIRF6的共聚焦细胞成像图

    Figure  6.  Confocal cell imaging of compounds NIRF2 and NIRF6

    表  1  化合物NIRF2与NIRF6在不同溶剂中的光学性质

    Table  1.   Optical properties of compounds NIRF2 and NIRF6 in different solvents

    化合物溶剂吸收波长/nm发射波长/nm摩尔消光系数Stokes 位移/nm
    NIRF2 甲苯 369 464 10500 95
    四氢呋喃 368 484 12400 116
    二氯甲烷 374 499 13700 125
    乙腈 366 519 12100 153
    二甲基亚砜 375 522 10900 147
    乙醇 369 529 19200 160
    NIRF6 甲苯 366 449 21200 83
    四氢呋喃 365 470 22000 105
    二氯甲烷 371 487 20200 116
    乙腈 366 510 19000 144
    二甲基亚砜 372 521 20200 149
    乙醇 370 526 19400 156
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出版历程
  • 收稿日期:  2021-10-31
  • 刊出日期:  2022-06-30

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