Identification of Unknown Inverted Singlet-Triplet Cores by High-Throughput Virtual Screening

被引:29
|
作者
Omar, Omer H. [1 ]
Xie, Xiaoyu [1 ]
Troisi, Alessandro [1 ]
Padula, Daniele [2 ]
机构
[1] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
[2] Univ Siena, Dipartimento Biotecnol Chim & Farm, I-53100 Siena, Italy
关键词
ACTIVATED DELAYED FLUORESCENCE; STATE PERTURBATION-THEORY; LIGHT-EMITTING-DIODES; SMILES; IMPLEMENTATION; FUNCTIONALS; FORMULATION; ACCEPTORS; SYSTEM;
D O I
10.1021/jacs.3c05452
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Molecules where the energy of the lowest excited singlet state is found below the energy of the lowest triplet state (inverted singlet-triplet molecules) are extremely rare. It is particularly challenging to discover new ones through virtual screening because the required wavefunction-based methods are expensive and unsuitable for high-throughput calculations. Here, we devised a virtual screening approach where the molecules to be considered with advanced methods are pre-selected with increasingly more sophisticated filters that include the evaluation of the HOMO-LUMO exchange integral and approximate CASSCF calculations. A final set of 7 candidates (0.05% of the initial 15 000) were verified to possess inversion between singlet and triplet states with state-of-the-art multireference methods (MS-CASPT2). One of them is deemed of particular interest because it is unrelated to other proposals made in the literature.
引用
收藏
页码:19790 / 19799
页数:10
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