Nitrogen-containing compound, organic electroluminescent device, and electronic apparatus
AssigneeShaanxi Lighte Optoelectronics Material Co., Ltd.
InventorsXianbin Xu, Lei Yang, Youngkook Kim
Life of this patent
Estimating the term…
Abstract
The present application relates to the technical field of organic electroluminescent materials, and provides a nitrogen-containing compound, an organic electroluminescent device including the nitrogen-containing compound, and an electronic apparatus. The nitrogen-containing compound of the present application has a core structure that is indolyl-fused phenothiazine/phenoxazine. The nitrogen-containing compound, when used as a host material of the luminescent layer of an organic electroluminescent device, can significantly improve the luminescence efficiency and service life of the device.
Claims16
A nitrogen-containing compound, having a structure shown in Formula 1:
- wherein:
- X is selected from S or O;
- group A is selected from a structure shown in Formula a-1 or a structure shown in Formula
- HAr is selected from substituted or unsubstituted arylene having 6 to 40 carbon atoms, and substituted or unsubstituted heteroarylene having 3 to 40 carbon atoms;
- Het is a nitrogen-containing heteroarylene having 3 to 20 carbon atoms;
- substituents in HAr are identical or different, and are each independently selected from the group consisting of deuterium, cyano, halogen, alkyl having 1 to 10 carbon atoms, deuterated alkyl having 1 to 10 carbon atoms, and aryl having 6 to 20 carbon atoms;
- L, L1, L2, and L3 are identical or different, and are each independently selected from the group consisting of single bond, substituted or unsubstituted arylene having 6 to 30 carbon atoms, and substituted or unsubstituted heteroarylene having 3 to 30 carbon atoms;
- Ar1 and Ar2 are identical or different, and are each independently selected from the group consisting of substituted or unsubstituted aryl having 6 to 40 carbon atoms, and substituted or unsubstituted heteroaryl having 3 to 40 carbon atoms;
- Ar3 is selected from the group consisting of hydrogen, substituted or unsubstituted aryl having 6 to 40 carbon atoms, and substituted or unsubstituted heteroaryl having 3 to 40 carbon atoms;
- Ar4 is selected from the group consisting of substituted or unsubstituted aryl having 6 to 40 carbon atoms, and substituted or unsubstituted heteroaryl having 3 to 40 carbon atoms, or Ar4 is single bond;
- substituents in L, L1, L2, L3, Ar1, Ar2, Ar3, and Ar4 are identical or different, and are each independently selected from the group consisting of deuterium, cyano, halogen, alkyl having 1 to 10 carbon atoms, haloalkyl having 1 to 10 carbon atoms, deuterated alkyl having 1 to 10 carbon atoms, trialkylsilyl having 3 to 12 carbon atoms, triphenylsilyl, aryl having 6 to 20 carbon atoms, heteroaryl having 3 to 20 carbon atoms, phosphonyl having 6 to 20 carbon atoms, cycloalkyl having 3 to 10 carbon atoms, alkoxy having 1 to 10 carbon atoms, alkylthio having 1 to 10 carbon atoms, aryloxy having 6 to 20 carbon atoms, and arylthio having 6 to 20 carbon atoms;
- and optionally, in Ar1, Ar2, Ar3, and Ar4, any two adjacent substituents form a saturated or unsaturated 3 to 15-membered ring;
- each R1, each R2, and each R3 is identical or different, and is independently selected from the group consisting of deuterium, cyano, halogen, alkyl having 1 to 10 carbon atoms, haloalkyl having 1 to 10 carbon atoms, deuterated alkyl having 1 to 10 carbon atoms, trialkylsilyl having 3 to 12 carbon atoms, aryl having 6 to 20 carbon atoms, heteroaryl having 3 to 20 carbon atoms, and cycloalkyl having 3 to 10 carbon atoms;
- and optionally, any two adjacent groups form a benzene ring;
- and
- n1 represents the number of R1, and is selected from 0, 1, 2, 3, or 4;
- n2 represents the number of R2, and is selected from 0, 1, 2, or 3;
- n3 represents the number of R3, and is selected from 0, 1, 2, 3, or 4.
Dependencies are inferred from the claim text.