Cañizares-Espada Elena, Pérez de Bustos Gema, Naoda Koji, Osuka Atsuhiro, Torres Tomás, Rodríguez-Morgade M Salomé
Departamento de Química Orgánica, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.
Department of Chemistry, Graduate School of Science, Kyoto University, 606-8502 Kyoto, Japan.
Org Lett. 2024 Feb 2;26(4):955-959. doi: 10.1021/acs.orglett.3c04320. Epub 2024 Jan 18.
A subporphyrazine (SubPz)-dithienylethene (DTE) photochromic device with and states, was developed and characterized. In this device, the DTE unit can reversibly switch the SubPz absorbance from green to near-infrared [λ (o/c) = 527 nm/740 nm], as well as the SubPz fluorescence and singlet oxygen quantum yields. The core of this design involves using a highly tunable SubPz chromophore that shares its quasi-isolated ethene moiety with a DTE photoswitch.
一种具有开和关两种状态的亚卟啉(SubPz)-二噻吩乙烯(DTE)光致变色器件被研发并进行了表征。在该器件中,DTE单元可将SubPz的吸光度从绿色可逆地切换至近红外[λ(开/关)=527纳米/740纳米],同时还能切换SubPz的荧光和单线态氧量子产率。该设计的核心在于使用一种高度可调谐的SubPz发色团,它与一个DTE光开关共享其准孤立的乙烯部分。