紧身衣
激发态
发光
激子
圆二色性
手性(物理)
化学
含时密度泛函理论
对映体
谱线
分子物理学
基态
原子物理学
物理
荧光
结晶学
立体化学
光学
凝聚态物理
量子力学
对称性破坏
手征对称破缺
Nambu–Jona Lasinio模型
作者
Francesco Zinna,Torsten Bruhn,Ciro A. Guido,Johannes Ahrens,Martin Bröring,Lorenzo Di Bari,Gennaro Pescitelli
标识
DOI:10.1002/chem.201602684
摘要
Abstract With our new home‐built circularly polarized luminescence (CPL) instrument, we measured fluorescence and CPL spectra of the enantiomeric pairs of two quasi‐isomeric BODIPY DYEmers 1 and 2 , endowed with axial chirality. The electronic circular dichroism (ECD) and CPL spectra of these atropisomeric dimers are dominated by the exciton coupling between the main π–π* transitions (550–560 nm) of the two BODIPY rings. Compound 1 has strong ECD and CPL spectra ( g lum =4×10 −3 ) well reproduced by TD‐DFT and SCS‐CC2 (spin‐component scaled second‐order approximate coupled‐cluster) calculations using DFT‐optimized ground‐ and excited‐state structures. Compound 2 has weaker ECD and CPL spectra ( g lum =4×10 −4 ), partly due to the mutual cancellation of electric–electric and electric–magnetic exciton couplings, and partly to its conformational freedom. This compound is computationally very challenging. Starting from the optimized excited‐state geometries, we predicted the wrong sign for the CPL band of 2 using TD‐DFT with the most recommended hybrid and range‐separated functionals, whereas SCS‐CC2 or a DFT functional with full exact exchange provided the correct sign.
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