IP Library Granted Patent US 10,411,202
Granted Patent B2
US 10,411,202 · App. 15/989,356 · Granted Sep 10, 2019

Tridentate cyclometalated metal complexes with six-membered coordination rings

Inventors: Jian Li (Tempe, AZ); Zhi-Qiang Zhu (Mesa, AZ)
Assignee: ARIZON BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
H01L51/0087C07F15/0086C09K11/06C09K2211/1029C09K2211/1044C09K2211/185H01L51/42H01L51/5016Y02E10/549
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Quick Facts
Patent No.
US 10,411,202
App. No.
15/989,356
Granted
Sep 10, 2019
Kind
B2
Abstract

Tridentate cyclometalated complexes with rigid six-membered coordination rings of General Formula I having tunable emission wavelengths in the visible range. These emitters are suitable for full color displays and lighting applications.

Claims (40)

1. A complex represented by Formula 5:

wherein:

M is Pt(II), Pd(II), Ir(I), Rh(I), or Au(II),

x=0 or 1, and when x=0, Y 3e is directly linked to Y 3b ;

y=0 or 1, and when y=0, Y 2a is directly linked to Y 4b ;

z=0 or 1, and when m=0, Y 2c is directly linked to Y 2d ;

each of Ar 1 , Ar 2 , and Ar 3 independently represents five-membered heteroaryl or six-membered aryl or heteroaryl,

each n is independently an integer of 1 to 4, valency permitting,

p is 4,

each R 1 , R 2 , R 3 , R 5 , and R 6 is independently hydrogen, halogen, hydroxyl, amino, nitro, thiol, or substituted or unsubstituted alkyl, alkoxyl, alkenyl, alkynyl, heteroaryl, or aryl, and any two of R 1 , any two of R 2 , any two of R 3 , any two of R 5 , and any two of R 6 are optionally linked together,

Y 1a is O, S, NR 2a , C, CR 2a , CR 2b R 2c , PR 2a , AsR 2a , BR 2a , or SiR 2d R 2e , where each of R 2a , R 2b , R 2c , R 2d , and R 2e is independently hydrogen, halogen, or substituted or unsubstituted alkyl, alkenyl, alkynyl, or aryl;

Y 1b is O, S, NR 3a , C, CR 3a , CR 3b R 3c , PR 2a , AsR 2a , BR 2a , P(O)R 2a , AS(O)R 2a , or SiR 3d R 3e , where each of R 3a , R 3b , R 3c , R 3d , and R 3e is independently hydrogen, halogen, or substituted or unsubstituted alkyl, alkenyl, alkynyl, or aryl,

each of Y 2a and Y 2d is independently C, N, NR 4a , or CR 4b , where each of R 4a and R 4b is independently hydrogen, hydroxyl, amino, nitro, thiol, or substituted or unsubstituted C 1 -C 4 alkyl, alkoxy, or aryl;

each of Y 2b and Y 2c is independently C or N,

each of Y 3a , Y 3b , Y 3c , Y 3d and Y 3e is independently C, N, O, S, NR 5a , PR 5b , AsR 5c , SiR 5d R 5e , BR 5f , or CR 5g , where each of R 5a , R 5b , R 5c , R 5d , R 5e , R 5f , and R 5g is independently hydrogen or substituted or unsubstituted C 1 -C 4 alkyl or aryl; or ZR 6a R 6b ; Z is C or Si; and each of R 6a and R 6b is independently substituted or unsubstituted C 1 -C 4 alkyl or aryl,

each of Y 4a , Y 4b , Y 4c , and Y 4d is independently N, NR 4e , C, or CR 4f , where each of R 4e and R 4f is independently hydrogen, hydroxyl, amino, nitro, thiol, or substituted or unsubstituted C 1 -C 4 alkyl, alkoxy, or aryl,

Y is halogen, OCOR 7a , OR 7b , SR 7c , NR 7d R 7e , CO, NR 7f , PR 7g , AsR 7h R 7i R 7j , C≡CR 7k , substituted or unsubstituted: pyridine, imidazole, pyrazole, oxazole, thiazole, isoxazole, or quinoline, where each of R 7a , R 7b , R 7c , R 7d , R 7e , R 7f , R 7g , R 7h , R 7i , R 7j and R 7k is independently, acetylacetonate, pyridine, imidazole or substituted or unsubstituted alkyl, alkenyl, alkynyl, aryl, or trisubstituted phosphine.

2. The complex of claim 1 , wherein the complex is represented by one of the following structures:

wherein:

U is O, S, NR, PR, AsR, CR 2 , SiR 2 , or BR,

M is Pt(II) or Pd(II);

each R is independently hydrogen, halogen, or substituted or unsubstituted alkyl, alkenyl, alkynyl, or aryl; and

each Ar 1 is independently selected from the group consisting of substituted or unsubstituted aryl and heteroaryl.

3. The complex of claim 1 , wherein the complex is represented by one of the following structures:

wherein:

U is O, S, NR, PR, AsR, CR 2 , SiR 2 , or BR;

M is Rh(I) or Ir(I);

each R is independently selected from the group consisting o hydrogen, halogen, or substituted or unsubstituted alkyl, alkenyl, alkynyl, or aryl; and

each Ar 1 is substituted or unsubstituted aryl or heteroaryl.

4. The complex of claim 1 , wherein the complex is represented by one of the following structures:

wherein:

U is O, S, NR, PR, AsR, CR 2 , SiR 2 , or BR,

M is Au(III);

each R is independently hydrogen, halogen, substituted or unsubstituted alkyl, alkenyl, alkynyl, or aryl; and

each Ar 1 is independently substituted or unsubstituted aryl or heteroaryl.

5. A light emitting device comprising the complex of claim 1 .

6. An OLED device comprising the complex of claim 1 .

7. The OLED device of claim 6 , wherein the device is a phosphorescent OLED device.

8. A photovoltaic device comprising the complex of claim 1 .

9. A luminescent display device comprising the complex of claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2018
From: LI, JIAN; ZHU, ZHI-QIANG
To: ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
Reel/Frame 046305/0378 →
Continuity (4)
Continuation 15355837 · Nov 18, 2016
Continuation 14808190 · Jul 24, 2015
Provisional Application 62029737 · Jul 28, 2014
Related Publication 20180277777A1 · Sep 27, 2018
Cited By (12)
US 12,193,327 US 12,221,573 US 12,232,411 US 12,302,745 US 12,312,366 US 12,448,405 US 12,492,336 US 12,503,644 US 12,534,462 US 12,545,678 US 12,565,486 US 12,643,919