Torsion Angle Analysis of a Thermally Activated Delayed Fluorescence Emitter in an Amorphous State Using Dynamic Nuclear Polarization Enhanced Solid-State NMR

被引:8
|
作者
Suzuki, Katsuaki [1 ]
Kaji, Hironori [1 ]
机构
[1] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
关键词
CHEMICAL-SHIFT ANISOTROPY; THIN-FILMS; SI-29; NMR; POLYMERS; SINGLET; DIODES; BULK;
D O I
10.1021/jacs.3c05204
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The torsion angle between donor and acceptor segmentsof a thermallyactivated delayed fluorescence (TADF) molecule is one of the mostcritical factors in determining the performance of TADF-based organiclight-emitting diodes (OLEDs) because the torsion angle affects notonly the energy gap between the singlet and triplet but also the oscillatorstrength and spin-orbit coupling. However, the torsion angleis difficult to analyze, because organic molecules are in an amorphousstate in OLEDs. Here, we determined the torsion angle of a highlyefficient TADF emitter, DACT-II, in an amorphous state by dynamicnuclear polarization enhanced solid-state NMR measurements. From theexperimentally obtained chemical shift principal values of N-15 on carbazole, we determined the average torsion angle to be 52 & DEG;.Such quantification of the torsion angles in TADF molecules in amorphoussolids will provide deep insight into the TADF mechanism in amorphousOLEDs.
引用
收藏
页码:16324 / 16329
页数:6
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