系统间交叉
光化学
阳离子聚合
化学
哌嗪
光敏剂
超分子化学
电子转移
激进的
单独一对
超氧化物
分子
有机化学
激发态
物理
酶
核物理学
单重态
作者
Wenping Zhu,Zhen Ding,Shaoxun Guo,Wu‐Jie Guo,Shirong Yan,Bin Liu,Hui Li,Zhen Liu,Ben Zhong Tang,Hui‐Qing Peng
出处
期刊:Small
[Wiley]
日期:2024-01-04
卷期号:20 (24): e2309424-e2309424
被引量:12
标识
DOI:10.1002/smll.202309424
摘要
Type-I photosensitizers (PSs) can generate free radical anions with a broad diffusion range and powerful damage effect, rendering them highly desirable in various areas. However, it still remains a recognized challenge to develop pure Type-I PSs due to the inefficiency in producing oxygen radical anions through the collision of PSs with nearby substrates. In addition, regulating the generation of oxygen radical anions is also of great importance toward the control of photosensitizer (PS) activities on demand. Herein, a piperazine-based cationic Type-I PS (PPE-DPI) that exhibits efficient intersystem crossing and subsequently captures oxygen molecules through binding O2 to the lone pair of nitrogen in piperazine is reported. The close spatial vicinity between O2 and PPE-DPI strongly promotes the electron transfer reaction, ensuring the exclusive superoxide radical (O2 •-) generation via Type-I process. Particularly, PPE-DPI with cationic pyridine groups is able to associate with cucurbit[7]uril (CB[7]) through host-guest interactions. Thus, supramolecular assembly and disassembly are easily utilized to realize switchable O2 •- generation. This switchable Type-I PS is successfully employed in photodynamic antibacterial control.
科研通智能强力驱动
Strongly Powered by AbleSci AI