The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules

被引：226

作者：

Ward, Jonathan S. ^{[1
]}

Nobuyasu, Roberto S. ^{[2
]}

Batsanov, Andrei S. ^{[1
]}

Data, Przemyslaw ^{[2
]}

Monkman, Andrew P. ^{[2
]}

Dias, Fernando B. ^{[2
]}

Bryce, Martin R. ^{[1
]}

机构：

[1] Univ Durham, Dept Chem, South Rd, Durham DH1 3LE, England

[2] Univ Durham, Dept Phys, Durham DH1 3LE, England

来源：

CHEMICAL COMMUNICATIONS | 2016年 / 52卷 / 12期

基金：

英国工程与自然科学研究理事会;

关键词：

LIGHT-EMITTING-DIODES; EMISSION; ELECTROLUMINESCENCE; EFFICIENCY; DESIGN; OLEDS;

D O I：

10.1039/c5cc09645f

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A series of phenothiazine-dibenzothiophene-S, S-dioxide charge-transfer molecules have been synthesized. Increasing steric restriction around the donor-acceptor bond significantly alters contributions from TADF and phosphorescence. Bulky substituents on the 1-(and 9) position(s) of the phenothiazine result in no TADF in the solid state; instead strong phosphorescence is observed at ambient temperature.

引用

页码：2612 / 2615

页数：4

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