化学
三氟丙酮
激发态
镧系元素
反应性(心理学)
激发
分子
配体(生物化学)
光化学
基态
计算化学
原子物理学
有机化学
离子
医学
生物化学
受体
电气工程
病理
萃取(化学)
物理
工程类
替代医学
溶剂萃取
作者
Maksim Y. Livshits,Nikki J. Wolford,Jenny K. Banh,Molly M. MacInnes,Samuel M. Greer,J. S. Raaj Vellore Winfred,Kenneth Hanson,Thaige P. Gompa,Benjamin W. Stein
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-08-13
卷期号:62 (34): 13712-13721
被引量:5
标识
DOI:10.1021/acs.inorgchem.3c00717
摘要
A series of four lanthanide thenoyltrifluoroacetone (TTA) complexes consisting of two f0 (La3+ and Ce4+) and two f1 (Ce3+) complexes was examined using steady-state and time-resolved spectroscopic techniques. The wide range of spectroscopic techniques presented herein have enabled us to discern the nature of the excited states (charge transfer, CT vs ligand localized, LL) as well as construct a Jablonski diagram for detailing the excited state reactivity within the series of molecules. The wavelength and excitation power dependence for these series of complexes are the first direct verification for the presence of simultaneous competing, noninteracting CT and LL excited states. Additionally, a computational framework is described that can be used to support spectroscopic assignments as a guide for future studies. Finally, the relationship between the obtained photophysics and possible photochemical separation mechanisms is described.
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