化学
旋转交叉
发色团
荧光
荧光团
合作性
自旋态
光化学
发光
接受者
自旋跃迁
分子
结晶学
光电子学
无机化学
光学
生物化学
物理
有机化学
凝聚态物理
作者
Junchuang Feng,Xiaoqin Wang,Liang Wang,Joseph Kfoury,Julianna Oláh,Shishen Zhang,Lifei Zou,Yun‐Nan Guo,Shufang Xue
标识
DOI:10.1021/acs.inorgchem.3c01789
摘要
Spin crossover (SCO) materials that possess switchable and cooperative fluorescence have long focused interest in photonic sensor devices to monitor the variations in the physicochemical parameters of the external environment. However, the lack of quantified cooperativity for the SCO transition operating in isolated molecules is detrimental to short-term technological applications. In this study, a pretwisted energy D–A system combining the deep-blue naphthalimide fluorophore (donor) and the FeN6 SCO chromophore (switchable acceptor) has been developed with the formula of Fe(naph-abpt)2(NCS)2·2DMF (1), where naph-abpt is N-[3,5-di(pyridin-2-yl)-4H-1,2,4-triazol-4-yl]-1,8-naphthalimide. Dual emission from the naphthalimide function based on its vibronic structure exhibits a different synergy effect with SCO, providing a new platform for ratiometric fluorescence thermosensing. Theoretical calculations and optical experimental results demonstrate an excellent correlation between luminescence intensity ratio signals and magnetic data of spin transition, promising a high sensitivity of the optical activity of the ligand to the spin state of the active iron(II) ions, with the maximum relative sensitivity as 0.7% K–1 around T1/2.
科研通智能强力驱动
Strongly Powered by AbleSci AI