Key Laboratory for Organic Electronics and Information Displays & Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM) , Nanjing University of Posts & Telecommunications , 9 Wenyuan Road , Nanjing 210023 , China.
Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM) , Nanjing Tech University (NanjingTech) , 30 South Puzhu Road , Nanjing 211816 , China.
ACS Appl Mater Interfaces. 2019 May 8;11(18):16311-16319. doi: 10.1021/acsami.9b02597. Epub 2019 Apr 25.
Low-band gap conjugated polymers with donor-acceptor (D-A) structures have emerged as second near-infrared (NIR-II) fluorescence probes for biological imaging. However, how to control the intramolecular charge transfer (ICT) to maintain the low band gap and improve the NIR-II fluorescence intensity is an urgent issue. Here, the quinoid polymers have been developed to effectively regulate the ICT for brighter NIR-II fluorescence signals. Thiophene repeat chain units of different lengths (T, 2T, and 3T) were utilized to link with electron-withdrawing ester-substituted thieno[3,4- b]thiophene (TT) to alter the density of the electron-withdrawing side groups for controlling the ICT. By increasing the thiophene chain length from TT-T to TT-3T, the density of the electron-withdrawing groups decreased and the ICT was weakened. In the case of NIR absorption and NIR-II emission, weakened ICT leads to brighter NIR-II fluorescence. After the preparation of the water-soluble quinoid polymer probes (CPs), TT-3T CPs with weak ICT exhibited the brightest NIR-II fluorescent signals among the three quinoid polymer probes. Several NIR-II biomedical imaging applications, including in vivo cell tracking, blood vascular system images, and lymphatic drainage mapping, show that the TT-3T CP-based nanoprobe had excellent characteristics of long-term stability and high NIR-II spatial resolutions in vivo.
具有给体-受体(D-A)结构的低带隙共轭聚合物已成为生物成像的第二代近红外二区(NIR-II)荧光探针。然而,如何控制分子内电荷转移(ICT)以保持低带隙并提高近红外二区荧光强度是一个紧迫的问题。在这里,开发了醌聚合物以有效调节 ICT,从而获得更亮的近红外二区荧光信号。利用不同长度的噻吩重复链单元(T、2T 和 3T)与吸电子酯取代的噻吩并[3,4-b]噻吩(TT)连接,改变吸电子侧基团的密度以控制 ICT。通过将噻吩链长度从 TT-T 增加到 TT-3T,吸电子基团的密度降低,ICT 减弱。在近红外吸收和近红外二区发射的情况下,较弱的 ICT 导致更亮的近红外二区荧光。在制备水溶性醌聚合物探针(CPs)后,具有较弱 ICT 的 TT-3T CPs 表现出三种醌聚合物探针中最亮的近红外二区荧光信号。几项近红外二区生物医学成像应用,包括体内细胞跟踪、血管系统图像和淋巴引流映射,表明基于 TT-3T CP 的纳米探针具有优异的长期稳定性和体内高近红外二区空间分辨率的特性。