AUTHOR=Jin Ruifa , Xin Jingfan 

TITLE=Rational Design of π-Conjugated Tricoordinated Organoboron Derivatives With Thermally Activated Delayed Fluorescent Properties for Application in Organic Light-Emitting Diodes

JOURNAL=Frontiers in Chemistry

VOLUME=8

YEAR=2020

URL=https://www.frontiersin.org/journals/chemistry/articles/10.3389/fchem.2020.577834

DOI=10.3389/fchem.2020.577834

ISSN=2296-2646

ABSTRACT=<p>A series of donor–acceptor (D–A) tricoordinated organoboron derivatives (<bold>1</bold>–<bold>10</bold>) have been systematically investigated for thermally activated delayed fluorescent (TADF)-based organic light-emitting diode (OLED) materials. The calculated results show that the designed molecules exhibit small singlet-triplet energy gap (Δ<italic>E</italic><sub>ST</sub>) values. Density functional theory (DFT) analysis indicated that the designed molecules display an efficient separation between donor and acceptor fragments because of a small overlap between donor and acceptor fragments on HOMOs and LUMOs. Furthermore, the delayed fluorescence emission color can be tuned effectively by introduction of different polycyclic aromatic fragments in parent molecule <bold>1</bold>. The calculated results show that molecules <bold>2</bold>, <bold>3</bold>, and <bold>4</bold> possess more significant Stokes shifts and red emission with small Δ<italic>E</italic><sub>ST</sub> values. Nevertheless, other molecules exhibit green (<bold>1</bold>, <bold>7</bold>, and <bold>8</bold>), light green (<bold>6</bold> and <bold>10</bold>), and blue (<bold>5</bold> and <bold>9</bold>) emissions. Meanwhile, they are potential ambipolar charge transport materials except that <bold>4</bold> and <bold>10</bold> can serve as electron and hole transport materials only, respectively. Therefore, we proposed a rational way for the design of efficient TADF materials as well as charge transport materials for OLEDs simultaneously.</p>