PHOSPHORESCENT MATERIALS

• US 20110227049A1
• Filed: 09/03/2009
• Published: 09/22/2011
• Est. Priority Date: 09/03/2008
• Status: Active Grant

• Current Assignee: Universal Display Corporation
• Original Assignee: Universal Display Corporation
• Inventors: Weaver, Michael S., Kwong, Raymond C., Alleyne, Bert, Fiordeliso, James, Xia, Chuanjun, Adamovich, Vadim, Brooks, Jason
• Granted Patent: US 8,519,384 B2
• Time in Patent Office: Days
• US Class Current: 257/40
• CPC Class Codes: C07F 15/0033 Iridium compounds
• CPC Class Codes: C09K 11/06 containing organic luminescent materials
• CPC Class Codes: C09K 2211/1007 Non-condensed systems
• CPC Class Codes: C09K 2211/1011 Condensed systems
• CPC Class Codes: C09K 2211/1059 containing three nitrogen atoms as heteroatoms
• CPC Class Codes: C09K 2211/1066 with sulfur
• CPC Class Codes: C09K 2211/1074 containing more than three nitrogen atoms as heteroatoms
• CPC Class Codes: C09K 2211/1092 containing sulfur as the only heteroatom
• CPC Class Codes: C09K 2211/185 of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd
• CPC Class Codes: H05B 33/14 characterised by the chemical or physical composition or the arrangement of the electroluminescent material , or by the simultaneous addition of the electroluminescent material in or onto the light source
• CPC Class Codes: H10K 2101/10 Triplet emission
• CPC Class Codes: H10K 50/11 characterised by the electroluminescent [EL] layers
• CPC Class Codes: H10K 85/324 comprising aluminium, e.g. Alq3
• CPC Class Codes: H10K 85/342 comprising iridium
• CPC Class Codes: H10K 85/622 containing four rings, e.g. pyrene
• CPC Class Codes: H10K 85/633 comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
• CPC Class Codes: H10K 85/6576 comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
• CPC Class Codes: Y02E 10/549 Organic PV cells

Abstract

Novel organic compounds containing a twisted aryl group are provided. In particular, the compounds provided contain a 2-phenylpyridine ligand having a twisted aryl group on the pyridine portion of the ligand. The compounds may be used in organic light emitting devices, particularly as emitting dopants. Devices comprising the compounds containing twisted aryl may demonstrate improved color, efficiency, stability and manufacturing. Additionally, methods are provided for making homoleptic Ir (III) compounds which may contain a twisted aryl.

Claims

1-116. -116. (canceled)

117. A compound comprising a ligand L having the structure:

118. The compound of claim 117, wherein the compound has the structure:

119. The compound of claim 117, wherein the metal M is Ir.

120. The compound of claim 117, wherein the compound is selected from the group consisting of:

121. The compound of claim 118, wherein the compound is selected from the group consisting of:

122. The compound of claim 117, wherein the compound is homoleptic.

123. The compound of claim 117, wherein the compound is heteroleptic.

124. The compound of claim 118, wherein L′

is selected from the group consisting of;

125. An organic light emitting device, comprising:

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, the organic layer further comprising a compound having the formula;

126. The device of claim 125, wherein the compound has the structure:

127. The device of claim 125, wherein the metal M is Ir.

128. The device of claim 125, wherein the compound is selected from the group consisting of:

129. The device of claim 125, wherein the compound is selected from the group consisting of:

130. The device of claim 125, wherein the organic layer is an emissive layer and the compound having the formula of Formula I is an emitting dopant.

131. The device of claim 130, wherein the organic layer further comprises a host.

132. A heteroleptic compound selected from the group consisting of

133. The compound of claim 132, wherein the compound is

134. An organic light emitting device, comprising:

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, the organic layer further comprising a compound selected from the group consisting of;

135. A method for making heteroleptic compounds, comprising:

reacting

136. A heteroleptic complex having the formula Ir(L_A-B)₂(L_C-D),

wherein L_A-B is