Understanding Aggregation-Induced Emission in Molecular Crystals: Insights from Theory

被引:54
作者
Presti, Davide [1 ]
Wilbraham, Liam [2 ]
Targa, Cecilia [1 ]
Labat, Frederic [2 ]
Pedone, Alfonso [1 ]
Menziani, Maria Cristina [1 ]
Ciofini, Ilaria [2 ]
Adamo, Carlo [2 ]
机构
[1] Univ Modena & Reggio Emilia, Dipartimento Sci Chim & Geol, 103 Via G Campi, I-41125 Modena, Italy
[2] PSL Res Univ, IRCP, CNRS Chim ParisTech, 11 Rue P & M Curie, F-75005 Paris 05, France
关键词
SALICYLIDENE ANILINE; VIBRONIC COUPLINGS; TD-DFT; ANTHRAQUINONES; MECHANISM; IMPACT; MODEL;
D O I
10.1021/acs.jpcc.7b00488
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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.
引用
收藏
页码:5747 / 5752
页数:6
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