卟啉
激进的
极化(电化学)
电子
旋转
光化学
化学
连接器
猝灭(荧光)
化学物理
材料科学
物理
荧光
计算机科学
有机化学
凝聚态物理
光学
物理化学
操作系统
量子力学
作者
Koki Nishimura,Reiya Yabuki,Tomoyuki Hamachi,Nobuo Kimizuka,Kenichiro Tateishi,Т. Уесака,Nobuhiro Yanai
标识
DOI:10.1021/acs.jpcb.2c07936
摘要
Dynamic electron polarization (DEP), induced by quenching of photoexcited species by stable radicals, can hyperpolarize electron spins in solution at room temperature. Recently, development of technologies based on electron spin polarization such as dynamic nuclear polarization (DNP) has been progressing, where it is important to design molecules that achieve long-lasting DEP in addition to high DEP. Hybridization by linking dyes and radicals is a promising approach for efficient DEP, but strong interactions between neighboring dyes and radicals often result in the rapid decay of DEP. In this study, we introduce a flexible linker into the hybrid system of porphyrin and TEMPO to achieve both efficient DEP and long-lasting DEP. The structural flexibility of the linker switches the interaction between the radical and the triplet, which promotes the DEP process by bringing the radical and the triplet into close proximity, while avoiding abrupt relaxation due to strong interactions. As a result, the new hybridized system exhibits a larger DEP than the unlinked system, while at the same time achieving a DEP lasting more than 10 μs.
科研通智能强力驱动
Strongly Powered by AbleSci AI