深铬移
激发态
分子内力
准分子
荧光
化学物理
发光
分子
聚集诱导发射
光化学
亮度
化学
磷光
材料科学
分子物理学
原子物理学
光电子学
光学
物理
立体化学
有机化学
作者
Davide Lo Presti,Liam Wilbraham,Cecilia Targa,Frédéric Labat,Alfonso Pedone,Maria Cristina Menziani,Ilaria Ciofini,Carlo Adamo
标识
DOI:10.1021/acs.jpcc.7b00488
摘要
Aggregation-induced emission can often be explained via the restriction of intramolecular rotation paradigm and/or excimer formation. The enhanced luminescence recently observed for aggregates of fluorenone derivatives are no exception. In this work, however, we use a recently developed excited-state electrostatic embedding technique to demonstrate that enhanced emission in diphenylfluorenone can be rationalized by considering a single-molecule process, in which the field induced by the crystalline environment at the excited state enhances the relative brightness of otherwise poorly emissive states, resulting in both enhanced fluorescence and a substantial bathochromic shift in comparison with emission in dilute solution.
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