Zhao Zhongli, Lin Hailong, Yang Tianshu, Zhang Lulu, Liu Qingyi, Zhang Chun, Qian Fengyu
College of Chemistry and Chemical Engineering, Lanzhou Jiaotong University Lanzhou 730070 P. R. China
State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, College of Chemistry and Chemical Engineering, Lanzhou University Lanzhou 730000 P. R. China.
RSC Adv. 2024 Mar 1;14(11):7430-7439. doi: 10.1039/d3ra07310f. eCollection 2024 Feb 29.
Hydrotalcite intercalated nanohybrid has served as a vital phosphorescent photosensitizer owing to remarkable O quantum yield and high cell mortality performance. However, it is rather difficult for potential large or complex guest phosphors to directly intercalate into the hydrotalcite gallery. Hence, it is necessary to regulate the interlayer microenvironment of hydrotalcites firstly for outstanding photosensitive properties. Herein, two isomers, 5,5'BDA and 4,4'BDA, with distinctive dual coordinative features were selected to modify the layer microenvironment of the LGdH gallery and induce the introduction of prospective Gd(HPhN) phosphorescent complexes into hydrotalcite through two different coordination effects successively. A LGdH-BDA-Gd(HPhN) intercalated nanohybrid phosphorescent photosensitizer was successfully obtained. The results indicated that the more efficient improvement was observed from 5,5'BDA due to offering a more spacious and stable space. Specifically, LGdH-5,5'BDA-Gd(HPhN) showed significantly better room temperature phosphorescence properties than LGdH-4,4'BDA-Gd(HPhN), whose lifetime was nearly 15 times longer than the latter. Additionally, the LGdH-5,5'BDA-Gd(HPhN) system displayed superior singlet oxygen generation under 460 nm irradiation (the quantum yield = 0.48) and outstanding photodynamic therapy performance in tumor cells. LGdH presented more remarkable enhancement performance on the RTP properties of the luminescent molecules. This work provides a novel platform for designing a high-performance hydrotalcite intercalated nanohybrid phosphorescent photosensitizer through coordination induction to regulate the layer microenvironment.
水滑石插层纳米杂化物因其显著的磷光量子产率和高细胞杀伤性能,已成为一种重要的磷光光敏剂。然而,潜在的大型或复杂客体磷光体直接插入水滑石层间相当困难。因此,首先有必要调节水滑石的层间微环境以获得优异的光敏性能。在此,选择具有独特双配位特征的两种异构体5,5'BDA和4,4'BDA来修饰LGdH层间的微环境,并通过两种不同的配位效应依次诱导将预期的Gd(HPhN)磷光配合物引入水滑石中。成功获得了LGdH-BDA-Gd(HPhN)插层纳米杂化物磷光光敏剂。结果表明,5,5'BDA由于提供了更宽敞和稳定的空间,其改善效果更显著。具体而言,LGdH-5,5'BDA-Gd(HPhN)的室温磷光性能明显优于LGdH-4,4'BDA-Gd(HPhN),其寿命比后者长近15倍。此外,LGdH-5,5'BDA-Gd(HPhN)体系在460 nm光照下表现出优异的单线态氧生成能力(量子产率 = 0.48)以及在肿瘤细胞中的出色光动力治疗性能。LGdH对发光分子的室温磷光性能表现出更显著的增强作用。这项工作通过配位诱导调节层间微环境,为设计高性能水滑石插层纳米杂化物磷光光敏剂提供了一个新平台。