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非共价聚合激活的超稳定近红外室温磷光能量转移组装体在水溶液中。

Noncovalent Polymerization-Activated Ultrastrong Near-Infrared Room-Temperature Phosphorescence Energy Transfer Assembly in Aqueous Solution.

机构信息

College of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin, 300071, P. R. China.

出版信息

Adv Mater. 2022 Sep;34(38):e2203534. doi: 10.1002/adma.202203534. Epub 2022 Aug 17.

DOI:10.1002/adma.202203534
PMID:35771589
Abstract

Noncovalent macrocycle-confined supramolecular purely organic room-temperature phosphorescence (RTP) is a current research hotspot. Herein, a high-efficiency noncovalent polymerization-activated near-infrared (NIR)-emissive RTP-harvesting system in aqueous solution based on the stepwise confinement of cucurbit[7]uril (CB[7]) and β-cyclodextrin-grafted hyaluronic acid (HACD), is reported. Compared with the dodecyl-chain-bridged 6-bromoisoquinoline derivative (G), the dumbbell-shaped assembly G⊂CB[7] presents an appeared complexation-induced RTP signal at 540 nm via the first confinement of CB[7]. Subsequently, benefitting from the stepwise confinement encapsulation of the β-cyclodextrin cavity, the subsequent noncovalent polymerization of the binary G⊂CB[7] assembly enabled by HACD can contribute to the further-enhanced RTP emission intensity approximately eight times in addition to an increased lifetime from 59.0 µs to 0.581 ms. Moreover, upon doping a small amount of two types of organic dyes, Nile blue or tetrakis(4-sulfophenyl)porphyrin as an acceptor into the supramolecular confinement assembly G⊂CB[7] @ HACD, efficient RTP energy transfer occurs accompanied by a long-lived NIR-emitting performance (680 and 710 nm) with a high donor/acceptor ratio. Intriguingly, the prepared RTP-harvesting system is successfully applied for targeted NIR imaging of living tumor cells by utilizing the targeting ability of hyaluronic acid, which provides a new strategy to create advanced water-soluble NIR phosphorescent materials.

摘要

非共价大环受限超分子纯有机室温磷光(RTP)是当前的研究热点。在此,报道了一种基于葫芦[7]脲(CB[7])和接枝透明质酸(HACD)的逐步限制的高效非共价聚合激活近红外(NIR)发射 RTP 收集体系的水溶液。与十二烷基桥接的 6-溴异喹啉衍生物(G)相比,哑铃形组装 G⊂CB[7]通过 CB[7]的第一次限制呈现出明显的复杂诱导的 RTP 信号在 540nm 处。随后,受益于β-环糊精空腔的逐步限制封装,随后由 HACD 引发的二元 G⊂CB[7]组装的非共价聚合可以进一步增强 RTP 发射强度,大约增加 8 倍,寿命从 59.0µs 增加到 0.581ms。此外,在超分子限制组装 G⊂CB[7]@HACD 中掺杂少量两种有机染料尼罗蓝或四(4-磺基苯基)卟啉作为受体时,会发生有效的 RTP 能量转移,并伴随着长寿命的近红外发射性能(680nm 和 710nm)和高供体/受体比。有趣的是,所制备的 RTP 收集系统通过利用透明质酸的靶向能力成功应用于活肿瘤细胞的靶向近红外成像,为创建先进的水溶性近红外磷光材料提供了新策略。

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