Phenylenediamine compounds for phosphorescent diazaborole metal complexes

Patent metadata

Field	Value
Publication number	US-9768397-B2
Application number	US-201514673227-A
Country	US
Kind code	B2
Filing date	Mar 30, 2015
Priority date	Mar 31, 2014
Publication date	Sep 19, 2017
Grant date	Sep 19, 2017

Abstract

The present disclosure generally relates to phenylenediamine compounds, which may be used as precursors in preparing diazaborole compounds and phosphorescent diazaborole metal complexes. The present disclosure also relates to diazaborole compounds, diazaborole metal complexes, and electroluminescent emission materials and electronic devices thereof. The present disclosure further relates to processes for preparing the phenylenediamine compounds and diazaborole metal complexes.

First claim

The invention claimed is:

1. A compound of Formula 1:

wherein
R 1 is selected from C 1-20 alkyl, C 2-20 alkenyl, C 2-20 alkynyl, and a 5 or 6 membered aryl or heteroaryl, each of which is optionally substituted with one or more substituents independently selected from halo, CN, NO 2 , C(O)R 2 , OR 2 , OS(O) 2 R 2 , NR 2 R 3 , SR 2 , aryl and heteroaryl;
R 2 and R 3 are each independently selected from hydrogen and C 1-6 alkyl;
each R 4 is independently selected from hydrogen, halo, CN, NO 2 , C(O)R 2 , OR 2 , OS(O) 2 R 2 , NR 2 R 3 , SR 2 , optionally substituted C 1-20 alkyl, optionally substituted C 2-20 alkenyl, optionally substituted C 2-20 alkynyl, optionally substituted 5 or 6 membered aryl or heteroaryl, and optionally two R 4 substituents from adjacent ring atoms are joined together to form an optionally substituted 5 or 6 membered aryl or heteroaryl ring; wherein R 2 and R 3 are each independently defined as above;
T is a tether group provided by a linear chain of 1 to 3 atoms independently selected from C, N, O, S, Si and B, each of which is optionally substituted with one or more substituents independently selected from hydrogen, halo, CN, NO 2 , ═O, C(O)R 2 , OR 2 , OS(O) 2 R 2 , NR 2 R 3 , SR 2 , optionally substituted C 1-10 alkyl, optionally substituted C 2-10 alkenyl, optionally substituted C 2-10 alkynyl and optionally substituted 5 or 6 membered aryl or heteroaryl, and optionally fused with a 3-6 membered carbocycle or heterocycle; and wherein R 2 and R 3 are each independently defined as above,
A is a monocyclic or bicyclic 5 or 6 membered heterocyclic ring containing a donor atom D and a ring atom A 1 , and optionally having 1 or 2 additional ring heteroatoms selected from O, S and N, wherein the heterocyclic ring is optionally substituted with 1 to 3 substituents independently selected from halo, CN, NO 2 , C(O)R 2 , OR 2 , OS(O) 2 R 2 , NR 2 R 3 , SR 2 , optionally substituted C 1-20 alkyl, optionally substituted C 2-20 alkenyl, optionally substituted C 2-20 alkynyl, and optionally substituted 5 or 6 membered aryl or heteroaryl; wherein R 2 and R 3 are each independently defined as above;
A 1 is selected from C, N and CR 7 ; wherein R 7 is selected from hydrogen, halo, CN, NO 2 , C(O)R 2 , OR 2 , OS(O) 2 R 2 , NR 2 R 3 , SR 2 , optionally substituted C 1-20 alkyl, optionally substituted C 2-20 alkenyl, optionally substituted C 2-20 alkynyl, optionally substituted 5 or 6 membered aryl or heteroaryl; R 2 and R 3 are each independently defined as above; and
D is a donor atom selected from N, O, S, P, Se and Te.

2. The compound of claim 1 , wherein R 1 is selected from optionally substituted C 1-10 alkyl and optionally substituted monocyclic 5 or 6 membered aryl or heteroaryl.

3. The compound of claim 1 , wherein T is a tether group provided by a linear chain of 1 to 3 atoms independently selected from —N(R 6 )—, —N(R 6 )—C(═O)—, —O—, —O—C(═O)—, —C(═O)—, —S—, —S(═O)—, —S(═O) 2 —, C 1-3 alkyl and C 2-3 alkenyl; wherein the C 1-3 alkyl and C 2-3 alkenyl are each optionally interrupted by a group selected from —N(R 6 )—, —N(R 6 )—C(═O)—, —O—, —O—C(═O)—, —C(═O)—, —S—, —S(═O)— and S(═O) 2 , and optionally substituted with one or more substituents independently selected from halo, CN, NO 2 , C(O)R 2 , OR 2 , OS(O) 2 R 2 , NR 2 R 3 , SR 2 , C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 1-10 alkylhalo, C 2-10 alkenylhalo and C 2-10 alkynylhalo, and optionally fused with a 3-6 membered carbocycle or heterocycle; and wherein R 6 is selected from hydrogen and C 1-10 alkyl.

4. The compound of claim 1 , wherein T is an optionally substituted, optionally fused C 1-3 alkyl.

5. The compound of claim 1 , wherein D is N.

6. The compound of claim 1 , wherein A is an optionally substituted pyridine group.

7. The compound of claim 1 , wherein each R 4 is hydrogen.

Assignees

• Commw Scient Ind Res Org

Inventors

• Bilyk Alexander
• Bown Mark
• Ueno Kazunori
• Groarke Michelle

Classifications

• H01L51/0085 Primary

  Electricity · mapped topic

• H01L51/0072

  Electricity · mapped topic

• C09K11/06 Primary

  containing organic luminescent materials · CPC title

• C07D471/04 Primary

  Ortho-condensed systems · CPC title

• H01L51/5012

  Electricity · mapped topic