IP Library › Granted Patent US 10,790,457
Granted Patent B2
US 10,790,457 · App. 15/711,525 · Granted Sep 29, 2020

Metal-assisted delayed fluorescent emitters containing tridentate ligands

Inventors: Jian Li (Tempe, AZ); Guijie Li (Hangzhou, CN)
Assignee: ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
H01L51/0087C07F1/12C07F9/65683C07F9/65685C07F15/006C07F15/0033C07F15/0073C07F15/0086C09K11/06H05B33/14C09K2211/1007C09K2211/1011C09K2211/1014C09K2211/1029C09K2211/1033C09K2211/1044C09K2211/1048C09K2211/1059C09K2211/1088C09K2211/1092C09K2211/1096C09K2211/185H01L51/5012H01L51/5016
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Quick Facts
Patent No.
US 10,790,457
App. No.
15/711,525
Granted
Sep 29, 2020
Kind
B2
Abstract

Tridentate platinum, palladium, and gold complexes of Formulas A-I and A-II and tridentate iridium and rhodium compounds of Formulas B-I, B-II, and B-III suitable for delayed fluorescent and phosphorescent or phosphorescent emitters in display and lighting applications.

Claims (40)

1. A compound represented by Formula A-1:

wherein:

M is Pt, Pd, or Au,

represents one of the following structures:

L 2 is substituted or unsubstituted phenyl,

L 3 is substituted or unsubstituted pyridyl,

R L4 is an inorganic anion or organic anion,

each of LP 1 , LP 2 , and LP 3 is independently present or absent, wherein at least one of LP 1 , LP 2 , or LP 3 is present and is an aromatic hydrocarbon, an aromatic hydrocarbon derivative, a polyphenyl hydrocarbon, a hydrocarbon with condensed aromatic nuclei, naphthalene, anthracene, phenanthrene, chrysene, pyrene, triphenylene, perylene, acenaphthene, tetracene, pentacene, tetraphene, coronene, fluorene, biphenyl, p-terphenyl, o-diphenylbenzene, m-diphenylbenzene, p-quaterphenyl, benzo[a]tetracene, benzo[k]tetraphene, indeno[1,2,3-cd]fluoranthene, tetrabenzo[de,hi,op,st]pentacene, arylethylene, arylacetylene, an arylacetylene derivative, a diarylethylene, a diarylpolyene, a diaryl-substituted vinylbenzene, a distyrylbenzene, a trivinylbenzene, an arylacetylene, a functional substitution product of stilbene, a five-, six- or seven-membered heterocyclic compound derivative, a furan derivative, a thiophene derivative, a pyrrole derivative, an aryl-substituted oxazole, a 1,3,4-oxadiazole, a 1,3,4-thiadiazole, an aryl-substituted 2-pyrazoline, an aryl-substituted pyrazole, a benzazole, 2H-benzotriazole, a substitution product of 2H-benzotriazole, a heterocycle with one, two or three nitrogen atoms, an oxygen-containing heterocycle, a coumarin, a coumarin derivative, a dye, an acridine dye, a xanthene dye, an oxazine, a thiazine, or a derivative thereof,

LP 1 , if present, is covalently bonded to L 1 directly,

LP 2 , if present, is covalently bonded to L 2 directly,

LP 3 , if present, is covalently bonded to L 3 directly,

A is O,

V 1 is N or C,

V 2 is C,

V 3 is N,

each of R a , R b , and R c is independently present or absent, and if present each of R a , R b and R c is independently a mono-, di-, tri-, or tetra-substitution, valency permitting, and each R a , R b , and R c is independently deuterium, halogen, hydroxyl, thiol, nitro, cyano, nitrile, isonitrile, sulfinyl, mercapto, sulfo, carboxyl, hydrazino; substituted or unsubstituted: aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, amino, monoalkylamino, dialkylamino, monoarylamino, diarylamino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, ureido, phosphoramide, silyl, polymeric; or any conjugate or combination thereof, and

two or more of R a are optionally linked together to form a cyclic structure, two or more of R b are optionally linked together to form a cyclic structure, and two or more of R c are optionally linked together to form a cyclic structure.

2. The compound of claim 1 , wherein is one of:

wherein each of R p , R q , and R r is independently hydrogen, deuterium, halogen, hydroxyl, thiol, nitro, cyano, nitrile, isonitrile, sulfinyl, mercapto, sulfo, carboxyl, hydrazino; substituted or unsubstituted: aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, amino, monoalkylamino, dialkylamino, monoarylamino, diarylamino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, ureido, phosphoramide, silyl, and polymeric; or any conjugate or combination thereof.

3. The compound of claim 1 , wherein:

represents one of the following structures:

and

R is hydrogen, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, monoalkylamino, dialkylamino, monoarylamino, diarylamino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, heteroaryl, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl, ureido, phosphoramide, mercapto, sulfo, carboxyl, hydrazino, substituted silyl, polymeric, or any conjugate or combination thereof.

4. The compound of claim 1 , wherein each of LP 1 , LP 2 and LP 3 , if present, independently represents one of the following structures:

aromatic hydrocarbons selected from the group consisting of:

and derivatives thereof,

arylethylenes and arylacetylenes selected from the group consisting of:

and derivatives thereof,

heterocyclic compounds selected from the group consisting of:

and derivatives thereof, and

other fluorescent luminophores selected from the group consisting of:

wherein:

each of R al , R bl , R cl , R dl , R el , R fl , R gl , R hl , and R il independently represents one of the following structures:

each R 1l , R 2l , R 3l , R 4l , R 5l , R 6l , R 7l , R 8l , R 9l , and R 10l is independently hydrogen, deuterium, halogen, hydroxyl, thiol, nitro, cyano, nitrile, isonitrile, sulfinyl, mercapto, sulfo, carboxyl, hydrazino; substituted or unsubstituted: aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, amino, monoalkylamino, dialkylamino, monoarylamino, diarylamino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, ureido, phosphoramide, silyl, polymeric; or any conjugate or combination thereof,

each of Y a , Y b , Y c , Y d , Y e , Y f , Y g , Y h , Y i , Y j , Y k , Y l , Y m , Y n , Y o , and Y p is independently C, N or B,

each of U a , U b , and U 2 is independently CH 2 , CR 1 R 2 , C═O, CH 2 , SiR 1 R 2 , GeH 2 , GeR 1 R 2 , NH, NR 3 , PH, PR 3 , R 3 P═O, AsR 3 , R 3 As═O, O, S, S═O, SO 2 , Se, Se═O, SeO 2 , BH, BR 3 , R 3 Bi═O, BiH, or BiR 3 ,

each of W, W a , and W b is independently CH, CR 1 , SiR 1 , GeH, GeR 1 , N, P, B, Bi, or Bi═O, and

each of R 1 , R 2 , and R 3 is independently hydrogen, aryl, cycloalkyl, cycloalkenyl, heterocyclyl, heteroaryl, alkyl, alkenyl, alkynyl, deuterium, halogen, hydroxyl, thiol, nitro, cyano, amino, monoalkylamino, dialkylamino, monoarylamino, diarylamino, alkoxy, aryloxy, haloalkyl, aralkyl, ester, nitrile, isonitrile, heteroaryl, alkoxycarbonyl, acylamino, alkoxycarbonylamino, aryloxycarbonylamino, sulfonylamino, sulfamoyl, carbamoyl, alkylthio, sulfinyl, ureido, phosphoramide, mercapto, sulfo, carboxyl, hydrazino, substituted silyl, or polymeric; or any conjugate or combination thereof.

5. A compound selected from the group consisting of:

6. The compound of claim 1 , wherein M is Pd or Au.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 29, 2018
From: LI, JIAN; LI, GUIJIE
To: ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
Reel/Frame 046742/0477 →
Continuity (3)
Continuation 14809981 · Jul 27, 2015
Provisional Application 62030235 · Jul 29, 2014
Related Publication 20180138428A1 · May 17, 2018
Cited By (9)
US 12,193,327 US 12,302,745 US 12,312,366 US 12,448,405 US 12,503,644 US 12,534,462 US 12,545,678 US 12,565,486 US 12,643,919