CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of copending U.S. patent application Ser. No. 16/861,725, filed Apr. 29, 2020, which claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 62/925,963, filed on Oct. 25, 2019, and U.S. Provisional Application No. 62/840,706, filed on Apr. 30, 2019, the entire contents of which are incorporated herein by reference

FIELD

The present disclosure generally relates to organometallic compounds and formulations and their various uses including as emitters in devices such as organic light emitting diodes and related electronic devices.

BACKGROUND

Opto-electronic devices that make use of organic materials are becoming increasingly desirable for various reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting diodes/devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials.

OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, illumination, and backlighting.

One application for phosphorescent emissive molecules is a full color display. Industry standards for such a display call for pixels adapted to emit particular colors, referred to as “saturated” colors. In particular, these standards call for saturated red, green, and blue pixels. Alternatively, the OLED can be designed to emit white light. In conventional liquid crystal displays emission from a white backlight is filtered using absorption filters to produce red, green and blue emission. The same technique can also be used with OLEDs. The white OLED can be either a single emissive layer (EML) device or a stack structure. Color may be measured using CIE coordinates, which are well known to the art.

SUMMARY

The present disclosure generally relates to transition metal complex compounds with novel ancillary ligands and methods of making these metal complex compounds and their various uses including as emissive dopants for improving performance of the OLED devices. Because of their unique electronic properties, the compounds show phosphorescent emission in red to near IR region and are useful as emitter materials in organic electroluminescence device.

In one aspect, the present disclosure provides a compound comprising a first ligand L_Aof

[Image Omitted]

wherein; R^A, R^B, and R^Care each independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein; two of R^A, R^B, and R^Care independently NRR′, OR, SR, or CO₂R, but R^Aand R^Bcannot be concurrently OR; R and R′ are each independently alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, aryl, heteroaryl, silyl, or combinations thereof, and two substituents can be joined or fused to form a ring; L_Ais coordinated to a metal M selected from the group consisting of Re, Ru, Os, Rh, Ir, Pd, Pt, Cu, Ag, and Cu; and the metal M is coordinated to additional maximum allowable number of ligands.

In another aspect, the present disclosure provides a formulation of the compound of the present disclosure. In another aspect, the present disclosure provides an OLED having an organic layer comprising the compound of the present disclosure. In yet another aspect, the present disclosure provides a consumer product comprising an OLED with an organic layer comprising the compound of the present disclosure.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an organic light emitting device.

FIG. 2 shows an inverted organic light emitting device that does not have a separate electron transport layer.

FIG. 3 shows the X-Ray diffraction analysis molecular diagram of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(OMe)CHC(CO₂Me)O}.

FIG. 4 shows X-Ray diffraction analysis molecular diagram of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(Me)CHC(CHCH₂)O}.

FIG. 5 shows the X-Ray diffraction analysis molecular diagram of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(Ph)CHC(p-C₆H₄Me)O}. FIG. 6 shows the PL spectrum of the inventive example Ir(L_B1-1)₂(L_A3241135) in PMMA film.

DETAILED DESCRIPTION
A. Terminology

Unless otherwise specified, the below terms used herein are defined as follows:

As used herein, the term “organic” includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices. “Small molecule” refers to any organic material that is not a polymer, and “small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances. For example, using a long chain alkyl group as a substituent does not remove a molecule from the “small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter. A dendrimer may be a “small molecule,” and it is believed that all dendrimers currently used in the field of OLEDs are small molecules.

As used herein, “top” means furthest away from the substrate, while “bottom” means closest to the substrate. Where a first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is “in contact with” the second layer. For example, a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.

As used herein, “solution processable” means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.

A ligand may be referred to as “photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material. A ligand may be referred to as “ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.

As used herein, and as would be generally understood by one skilled in the art, a first “Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is “greater than” or “higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative). On a conventional energy level diagram, with the vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. A “higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a “lower” HOMO or LUMO energy level.

As used herein, and as would be generally understood by one skilled in the art, a first work function is “greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a “higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.

The terms “halo,” “halogen,” and “halide” are used interchangeably and refer to fluorine, chlorine, bromine, and iodine. The term “acyl” refers to a substituted carbonyl radical (C(O)—R_s). The term “ester” refers to a substituted oxycarbonyl (—O—C(O)—R, or —C(O)—O—R_s) radical. The term “ether” refers to an —OR_sradical. The terms “sulfanyl” or “thio-ether” are used interchangeably and refer to a —SR_sradical. The term “sulfinyl” refers to a —S(O)—R_sradical. The term “sulfonyl” refers to a —SO₂—R_sradical. The term “phosphino” refers to a —P(R_s)₃radical, wherein each R_scan be same or different. The term “silyl” refers to a —Si(R_s)₃radical, wherein each R_scan be same or different. The term “boryl” refers to a —B(R_s)₂radical or its Lewis adduct —B(R_s)₃radical, wherein R_scan be same or different.

In each of the above, R_scan be hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, and combination thereof. Preferred R_sis selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, and combination thereof.

The term “alkyl” refers to and includes both straight and branched chain alkyl radicals. Preferred alkyl groups are those containing from one to fifteen carbon atoms and includes methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, and the like. Additionally, the alkyl group may be optionally substituted. The term “cycloalkyl” refers to and includes monocyclic, polycyclic, and spiro alkyl radicals. Preferred cycloalkyl groups are those containing 3 to 12 ring carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, bicyclo[3.1.1]heptyl, spiro[4.5]decyl, spiro[5.5]undecyl. adamantyl, and the like. Additionally, the cycloalkyl group may be optionally substituted. The terms “heteroalkyl” or “heterocycloalkyl” refer to an alkyl or a cycloalkyl radical, respectively, having at least one carbon atom replaced by a heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si and Se, preferably, O, S or N. Additionally, the heteroalkyl or heterocycloalkyl group may be optionally substituted.

The term “alkenyl” refers to and includes both straight and branched chain alkene radicals. Alkenyl groups are essentially alkyl groups that include at least one carbon-carbon double bond in the alkyl chain. Cycloalkenyl groups are essentially cycloalkyl groups that include at least one carbon-carbon double bond in the cycloalkyl ring. The term “heteroalkenyl” as used herein refers to an alkenyl radical having at least one carbon atom replaced by a heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si, and Se, preferably, O, S, or N. Preferred alkenyl, cycloalkenyl, or heteroalkenyl groups are those containing two to fifteen carbon atoms. Additionally, the alkenyl, cycloalkenyl, or heteroalkenyl group may be optionally substituted.

The term “alkynyl” refers to and includes both straight and branched chain alkyne radicals. Alkynyl groups are essentially alkyl groups that include at least one carbon-carbon triple bond in the alkyl chain. Preferred alkynyl groups are those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted.

The terms “aralkyl” or “arylalkyl” are used interchangeably and refer to an alkyl group that is substituted with an aryl group. Additionally, the aralkyl group may be optionally substituted.

The term “heterocyclic group” refers to and includes aromatic and non-aromatic cyclic radicals containing at least one heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si, and Se, preferably, O, S, or N. Hetero-aromatic cyclic radicals may be used interchangeably with heteroaryl. Preferred hetero-non-aromatic cyclic groups are those containing 3 to 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperidino, pyrrolidino, and the like, and cyclic ethers/thio-ethers, such as tetrahydrofuran, tetrahydropyran, tetrahydrothiophene, and the like. Additionally, the heterocyclic group may be optionally substituted.

The term “aryl” refers to and includes both single-ring aromatic hydrocarbyl groups and polycyclic aromatic ring systems. The polycyclic rings may have two or more rings in which two carbons are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is an aromatic hydrocarbyl group, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred aryl groups are those containing six to thirty carbon atoms, preferably six to twenty carbon atoms, more preferably six to twelve carbon atoms. Especially preferred is an aryl group having six carbons, ten carbons or twelve carbons. Suitable aryl groups include phenyl, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene, preferably phenyl, biphenyl, triphenyl, triphenylene, fluorene, and naphthalene. Additionally, the aryl group may be optionally substituted.

The term “heteroaryl” refers to and includes both single-ring aromatic groups and polycyclic aromatic ring systems that include at least one heteroatom. The heteroatoms include, but are not limited to O, S, N, P, B, Si, and Se. In many instances, O, S, or N are the preferred heteroatoms. Hetero-single ring aromatic systems are preferably single rings with 5 or 6 ring atoms, and the ring can have from one to six heteroatoms. The hetero-polycyclic ring systems can have two or more rings in which two atoms are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. The hetero-polycyclic aromatic ring systems can have from one to six heteroatoms per ring of the polycyclic aromatic ring system. Preferred heteroaryl groups are those containing three to thirty carbon atoms, preferably three to twenty carbon atoms, more preferably three to twelve carbon atoms. Suitable heteroaryl groups include dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine, preferably dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, triazine, benzimidazole, 1,2-azaborine, 1,3-azaborine, 1,4-azaborine, borazine, and aza-analogs thereof. Additionally, the heteroaryl group may be optionally substituted.

Of the aryl and heteroaryl groups listed above, the groups of triphenylene, naphthalene, anthracene, dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, pyrazine, pyrimidine, triazine, and benzimidazole, and the respective aza-analogs of each thereof are of particular interest.

The terms alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aralkyl, heterocyclic group, aryl, and heteroaryl, as used herein, are independently unsubstituted, or independently substituted, with one or more general substituents.

In many instances, the general substituents are selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, boryl, and combinations thereof.

In some instances, the preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, boryl, and combinations thereof.

In some instances, the more preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, alkoxy, aryloxy, amino, silyl, boryl, aryl, heteroaryl, sulfanyl, and combinations thereof.

In yet other instances, the most preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof.

The terms “substituted” and “substitution” refer to a substituent other than H that is bonded to the relevant position, e.g., a carbon or nitrogen. For example, when R¹represents mono-substitution, then one R¹must be other than H (i.e., a substitution). Similarly, when R¹represents di-substitution, then two of R¹must be other than H. Similarly, when R¹represents zero or no substitution, R¹, for example, can be a hydrogen for available valencies of ring atoms, as in carbon atoms for benzene and the nitrogen atom in pyrrole, or simply represents nothing for ring atoms with fully filled valencies, e.g., the nitrogen atom in pyridine. The maximum number of substitutions possible in a ring structure will depend on the total number of available valencies in the ring atoms.

As used herein, “combinations thereof” indicates that one or more members of the applicable list are combined to form a known or chemically stable arrangement that one of ordinary skill in the art can envision from the applicable list. For example, an alkyl and deuterium can be combined to form a partial or fully deuterated alkyl group; a halogen and alkyl can be combined to form a halogenated alkyl substituent; and a halogen, alkyl, and aryl can be combined to form a halogenated arylalkyl. In one instance, the term substitution includes a combination of two to four of the listed groups. In another instance, the term substitution includes a combination of two to three groups. In yet another instance, the term substitution includes a combination of two groups. Preferred combinations of substituent groups are those that contain up to fifty atoms that are not hydrogen or deuterium, or those which include up to forty atoms that are not hydrogen or deuterium, or those that include up to thirty atoms that are not hydrogen or deuterium. In many instances, a preferred combination of substituent groups will include up to twenty atoms that are not hydrogen or deuterium.

The “aza” designation in the fragments described herein, i.e. aza-dibenzofuran, aza-dibenzothiophene, etc. means that one or more of the C—H groups in the respective aromatic ring can be replaced by a nitrogen atom, for example, and without any limitation, azatriphenylene encompasses both dibenzo[f,h]quinoxaline and dibenzo[f,h]quinoline. One of ordinary skill in the art can readily envision other nitrogen analogs of the aza-derivatives described above, and all such analogs are intended to be encompassed by the terms as set forth herein.

As used herein, “deuterium” refers to an isotope of hydrogen. Deuterated compounds can be readily prepared using methods known in the art. For example, U.S. Pat. No. 8,557,400, Patent Pub. No. WO 2006/095951, and U.S. Pat. Application Pub. No. US 2011/0037057, which are hereby incorporated by reference in their entireties, describe the making of deuterium-substituted organometallic complexes. Further reference is made to Ming Yan, et al., Tetrahedron 2015, 71, 1425-30 and Atzrodt et al., Angew. Chem. Int. Ed. (Reviews) 2007, 46, 7744-65, which are incorporated by reference in their entireties, describe the deuteration of the methylene hydrogens in benzyl amines and efficient pathways to replace aromatic ring hydrogens with deuterium, respectively.

It is to be understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. phenyl, phenylene, naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g. benzene, naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent.

In some instance, a pair of adjacent substituents can be optionally joined or fused into a ring. The preferred ring is a five, six, or seven-membered carbocyclic or heterocyclic ring, includes both instances where the portion of the ring formed by the pair of substituents is saturated and where the portion of the ring formed by the pair of substituents is unsaturated. As used herein, “adjacent” means that the two substituents involved can be on the same ring next to each other, or on two neighboring rings having the two closest available substitutable positions, such as 2, 2′ positions in a biphenyl, or 1, 8 position in a naphthalene, as long as they can form a stable fused ring system.

B. The Compounds of the Present Disclosure

In one aspect, the present disclosure provides a compound comprising a first ligand L_Aof

[Image Omitted]

wherein; R^A, R^B, and R^Care each independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein; two of R^A, R^B, and R^Care independently NRR′, OR, SR, or CO₂R, but R^Aand R^Bcannot be concurrently OR; R and R′ are each independently alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, aryl, heteroaryl, silyl, or combinations thereof, and two substituents can be joined or fused to form a ring; LA is coordinated to a metal M selected from the group consisting of Re, Ru, Os, Rh, Ir, Pd, Pt, Cu, Ag, and Cu; and the metal M is coordinated to additional maximum allowable number of ligands.

In some embodiments of the compound, R^Aand R^Bare each independently NRR′, OR, SR, or CO₂R. In some embodiments, R^Cis a hydrogen or a substituent selected from the group consisting of the preferred general substituents defined herein.

In some embodiments of the compound, R^Aand R^Bare both NRR′. In some embodiments, R^Ais OR and R^Bis CO₂R. In some embodiments, R^Cis a hydrogen or an alkyl. In some embodiments, R^Aand R^Bare different.

In some embodiments of the compound, M is Ir or Pt.

In some embodiments of the compound, the first ligand L_Ahas a general formula L_AQ, where Q is an integer from 1 to 3241135, and L_Ais selected from the group consisting of L_A1to L_A3241135whose structures are defined as follows:

and wherein

R¹, R², and R³

L_AQ
based on Formula
where Q is
are defined as

L_A1to L_A6561

[Image Omitted]

Formula 1
Q = 81 (i − 1) + j, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj;

L_A6562to L_A13122

[Image Omitted]

Formula 2
Q = 81 (i − 1) + j + 6561, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj;

L_A13123to L_A19683

[Image Omitted]

Formula 3
Q = 81 (i − 1) + j + 13122, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj;

L_A19684to L_A26244

[Image Omitted]

Formula 4
Q = 81 (i − 1) + j + 19683, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj;

L_A26245to L_A32805

[Image Omitted]

Formula 5
Q = 81 (i − 1) + j + 26244, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj;

L_A32806to L_A39366

[Image Omitted]

Formula 6
Q = 81 (i − 1) + j + 32805, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj;

L_A39367to L_A45927

[Image Omitted]

Formula 7
Q = 81 (i − 1) + j + 39366, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj;

L_A45928to L_A52488

[Image Omitted]

Formula 8
Q = 81 (i − 1) + j + 45927, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj;

L_A52489to L_A583930

[Image Omitted]

Formula 9
Q = 81 (81 (i − 1) + j − 1) + k + 52488, wherein i is an integer from 1 to 81, j is an integer from 1 to 81, k is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj; R³= R^Dk;

L_A583931to L_A1115371

[Image Omitted]

Formula 10
Q = 81 (81 (i − 1) + j − 1) + k + 583930, wherein i is an integer from 1 to 81, j is an integer from 1 to 81, k is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj; R³= R^Dk;

L_A1115372to L_A1646812

[Image Omitted]

Formula 11
Q = 81 (81 (i − 1) + j − 1) + k + 1115372, wherein i is an integer from 1 to 81, j is an integer from 1 to 81, k is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj; R³= R^Dk;

L_A1646813to L_A2178253

[Image Omitted]

Formula 12
Q = 81 (81 (i − 1) + j − 1) + k + 1646812, wherein i is an integer from 1 to 81, j is an integer from 1 to 81, k is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj; R³= R^Dk;

L_A2178254to L_A2709694

[Image Omitted]

Formula 13
Q = 81 (81 (i − 1) + j − 1) + k + 2178253, wherein i is an integer from 1 to 81, j is an integer from 1 to 81, k is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj; R³= R^Dk;

L_A2709695to L_A3241135

[Image Omitted]

Formula 14
Q = 81 (81 (i − 1) + j − 1) + k + 2709694, wherein i is an integer from 1 to 81, j is an integer from 1 to 81, k is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj; R³= R^Dk;

L_A3241135to L_A3247695

[Image Omitted]

Formula 15
Q = 81 (i − 1) + j + 26244, wherein i is an integer from 1 to 81, j is an integer from 1 to 81.
R¹= R^Di; R²= R^Dj

where R^D1to R^D81have the following structures:

[Image Omitted]

In some embodiments, the compound has a formula of M(L_A)_x(L_B)_y(L_C)_z, where L_Band L_Care each a bidentate ligand; and wherein x is 1, 2, or 3; y is 0, 1, or 2; z is 0, 1, or 2; and x+y+z is the oxidation state of the metal M.

In some embodiments of the compound having the formula of M(L_A)_x(L_B)_y(L_C)_z, as defined above, the compound has a formula selected from the group consisting of Ir(L_A)₃, Ir(L_A)(L_B)₂, Ir(L_A)₂(L_B), Ir(L_A)₂(L_C), and Ir(L_A)(L_B)(L_C), where L_A, L_B, and L_Care different from each other.

In some embodiments of the compound having the formula of M(L_A)_x(L_B)_y(L_C)_zas defined above, the compound has a formula of Pt(L_A)(L_B), where L_Aand L_Bcan be the same or different. In some embodiments, L_Aand L_Bare connected to form a tetradentate ligand.

In some embodiments of the compound having the formula of M(L_A)_x(L_B)_y(L_C)_zas defined above, L_Band L_Care each a bidentate ligand, L_Band L_Care each independently selected from the group consisting of:

[Image Omitted]

wherein: Y¹to Y¹³are each independently selected from the group consisting of carbon and nitrogen; Y′ is selected from the group consisting of BR_e, NR_e, PR_e, O, S, Se, C═O, S═O, SO₂, CR_eR_f, SiR_eR_f, and GeR_eR_f; wherein R_eand R_fcan be fused or joined to form a ring; R_a, R_b, R_c, and R_deach independently represents zero, mono, or up to a maximum allowed substitution to its associated ring; each R_a, R_b, R_c, R_d, R_eand R_fis independently hydrogen or a substituent selected from the group consisting of the general substituents defined herein; and two adjacent substituents of R_a, R_b, R_c, and R_dcan be fused or joined to form a ring or form a multidentate ligand.

In some embodiments of the compound having the formula M(L_A)_x(L_B)_y(L_C)_zas defined above, L_Band L_Care each independently selected from the group consisting of:

[Image Omitted]

wherein: R_a′, R_b′, and R_c′ each independently represent zero, mono, or up to a maximum allowed substitution to its associated ring; each of R_a, R_b, R_c, R_N, R_a′, R_b′, and R_c′ is independently a hydrogen or selected from a substituent as described above; and two adjacent substituents of R_a′, R_b′, and R_c′ can be fused or joined to form a ring or form a multidentate ligand.

In some embodiments of the compound having the formula of M(L_A)_x(L_B)_y(L_C)_zas defined above, the compound has a formula Ir(L_A)(L_Bm-n)₂, where m is an integer from 1 to 200, n is an integer from 1 to 44, and the structures of L_Bm-nare defined as follows:

- L_Bm-1based on,

[Image Omitted]

L_Bm-2based on,

[Image Omitted]

L_Bm-3based on,

[Image Omitted]

L_Bm-4based on,

[Image Omitted]

L_Bm-5based on,

[Image Omitted]

L_Bm-6based on,

[Image Omitted]

L_Bm-7based on,

[Image Omitted]

L_Bm-8based on,

[Image Omitted]

L_Bm-9based on,

[Image Omitted]

L_Bm-10based on,

[Image Omitted]

L_Bm-11based on,

[Image Omitted]

L_Bm-12based on,

[Image Omitted]

L_Bm-13based on,

[Image Omitted]

L_Bm-14based on,

[Image Omitted]

L_Bm-15based on,

[Image Omitted]

L_Bm-16based on,

[Image Omitted]

L_Bm-17based on,

[Image Omitted]

L_Bm-18based on,

[Image Omitted]

L_Bm-19based on,

[Image Omitted]

L_Bm-20based on,

[Image Omitted]

L_Bm-21based on,

[Image Omitted]

L_Bm-22based on,

[Image Omitted]

L_Bm-23based on,

[Image Omitted]

L_Bm-24based on,

[Image Omitted]

L_Bm-25based on,

[Image Omitted]

L_Bm-26is based on

[Image Omitted]

L_Bm-27based on

[Image Omitted]

L_Bm-28is based on

[Image Omitted]

L_Bm-29based on

[Image Omitted]

L_Bm-30based on

[Image Omitted]

L_Bm-31based on

[Image Omitted]

L_Bm-32based on

[Image Omitted]

L_Bm-33based on

[Image Omitted]

L_Bm-34based on

[Image Omitted]

L_Bm-35based on

[Image Omitted]

L_Bm-36based on

[Image Omitted]

L_Bm-37based on

[Image Omitted]

L_Bm-38based on

[Image Omitted]

L_Bm-39based on

[Image Omitted]

L_Bm-40based on

[Image Omitted]

L_Bm-41based on

[Image Omitted]

L_Bm-42based on

[Image Omitted]

L_Bm-43based on

[Image Omitted]

and L_Bm-44based on

[Image Omitted]

wherein m is an integer from 1 to 200 and for each L_Bm, R^Eand G are defined as follows:

L_Bm
R^E
G

L_B1
R¹
G¹

L_B2
R²
G¹

L_B3
R³
G¹

L_B4
R⁴
G¹

L_B5
R⁵
G¹

L_B6
R⁶
G¹

L_B7
R⁷
G¹

L_B8
R⁸
G¹

L_B9
R⁹
G¹

L_B10
R¹⁰
G¹

L_B11
R¹¹
G¹

L_B12
R¹²
G¹

L_B13
R¹³
G¹

L_B14
R¹⁴
G¹

L_B15
R¹⁵
G¹

L_B16
R¹⁶
G¹

L_B17
R¹⁷
G¹

L_B18
R¹⁸
G¹

L_B19
R¹⁹
G¹

L_B20
R²⁰
G¹

L_B21
R¹
G⁵

L_B22
R²
G⁵

L_B23
R³
G⁵

L_B24
R⁴
G⁵

L_B25
R⁵
G⁵

L_B26
R⁶
G⁵

L_B27
R⁷
G⁵

L_B28
R⁸
G⁵

L_B29
R⁹
G⁵

L_B30
R¹⁰
G⁵

L_B31
R¹¹
G⁵

L_B32
R¹²
G⁵

L_B33
R¹³
G⁵

L_B34
R¹⁴
G⁵

L_B35
R¹⁵
G⁵

L_B36
R¹⁶
G⁵

L_B37
R¹⁷
G⁵

L_B38
R¹⁸
G⁵

L_B39
R¹⁹
G⁵

L_B40
R²⁰
G⁵

L_B41
R¹
G⁹

L_B42
R²
G⁹

L_B43
R³
G⁹

L_B44
R⁴
G⁹

L_B45
R⁵
G⁹

L_B46
R⁶
G⁹

L_B47
R⁷
G⁹

L_B48
R⁸
G⁹

L_B49
R⁹
G⁹

L_B50
R¹⁰
G⁹

L_B51
R¹
G²

L_B52
R²
G²

L_B53
R³
G²

L_B54
R⁴
G²

L_B55
R⁵
G²

L_B56
R⁶
G²

L_B57
R⁷
G²

L_B58
R⁸
G²

L_B59
R⁹
G²

L_B60
R¹⁰
G²

L_B61
R¹¹
G²

L_B62
R¹²
G²

L_B63
R¹³
G²

L_B64
R¹⁴
G²

L_B65
R¹⁵
G²

L_B66
R¹⁶
G²

L_B67
R¹⁷
G²

L_B68
R¹⁸
G²

L_B69
R¹⁹
G²

L_B70
R²⁰
G²

L_B71
R¹
G⁶

L_B72
R²
G⁶

L_B73
R³
G⁶

L_B74
R⁴
G⁶

L_B75
R⁵
G⁶

L_B76
R⁶
G⁶

L_B77
R⁷
G⁶

L_B78
R⁸
G⁶

L_B79
R⁹
G⁶

L_B80
R¹⁰
G⁶

L_B81
R¹¹
G⁶

L_B82
R¹²
G⁶

L_B83
R¹³
G⁶

L_B84
R¹⁴
G⁶

L_B85
R¹⁵
G⁶

L_B86
R¹⁶
G⁶

L_B87
R¹⁷
G⁶

L_B88
R¹⁸
G⁶

L_B89
R¹⁹
G⁶

L_B90
R²⁰
G⁶

L_B91
R¹¹
G⁹

L_B92
R¹²
G⁹

L_B93
R¹³
G⁹

L_B94
R¹⁴
G⁹

L_B95
R¹⁵
G⁹

L_B96
R¹⁶
G⁹

L_B97
R¹⁷
G⁹

L_B98
R¹⁸
G⁹

L_B99
R¹⁹
G⁹

L_B100
R²⁰
G⁹

L_B101
R¹
G³

L_B102
R²
G³

L_B103
R³
G³

L_B104
R⁴
G³

L_B105
R⁵
G³

L_B106
R⁶
G³

L_B107
R⁷
G³

L_B108
R⁸
G³

L_B109
R⁹
G³

L_B110
R¹⁰
G³

L_B111
R¹¹
G³

L_B112
R¹²
G³

L_B113
R¹³
G³

L_B114
R¹⁴
G³

L_B115
R¹⁵
G³

L_B116
R¹⁶
G³

L_B117
R¹⁷
G³

L_B118
R¹⁸
G³

L_B119
R¹⁹
G³

L_B120
R²⁰
G³

L_B121
R¹
G⁷

L_B122
R²
G⁷

L_B123
R³
G⁷

L_B124
R⁴
G⁷

L_B125
R⁵
G⁷

L_B126
R⁶
G⁷

L_B127
R⁷
G⁷

L_B128
R⁸
G⁷

L_B129
R⁹
G⁷

L_B130
R¹⁰
G⁷

L_B131
R¹¹
G⁷

L_B132
R¹²
G⁷

L_B133
R¹³
G⁷

L_B134
R¹⁴
G⁷

L_B135
R¹⁵
G⁷

L_B136
R¹⁶
G⁷

L_B137
R¹⁷
G⁷

L_B138
R¹⁸
G⁷

L_B139
R¹⁹
G⁷

L_B140
R²⁰
G⁷

L_B141
R¹
G¹⁰

L_B142
R²
G¹⁰

L_B143
R³
G¹⁰

L_B144
R⁴
G¹⁰

L_B145
R⁵
G¹⁰

L_B146
R⁶
G¹⁰

L_B147
R⁷
G¹⁰

L_B148
R⁸
G¹⁰

L_B149
R⁹
G¹⁰

L_B150
R¹⁰
G¹⁰

L_B151
R¹
G⁴

L_B152
R²
G⁴

L_B153
R³
G⁴

L_B154
R⁴
G⁴

L_B155
R⁵
G⁴

L_B156
R⁶
G⁴

L_B157
R⁷
G⁴

L_B158
R⁸
G⁴

L_B159
R⁹
G⁴

L_B160
R¹⁰
G⁴

L_B161
R¹¹
G⁴

L_B162
R¹²
G⁴

L_B163
R¹³
G⁴

L_B164
R¹⁴
G⁴

L_B165
R¹⁵
G⁴

L_B166
R¹⁶
G⁴

L_B167
R¹⁷
G⁴

L_B168
R¹⁸
G⁴

L_B169
R¹⁹
G⁴

L_B170
R²⁰
G⁴

L_B171
R¹
G⁸

L_B172
R²
G⁸

L_B173
R³
G⁸

L_B174
R⁴
G⁸

L_B175
R⁵
G⁸

L_B176
R⁶
G⁸

L_B177
R⁷
G⁸

L_B178
R⁸
G⁸

L_B179
R⁹
G⁸

L_B180
R¹⁰
G⁸

L_B181
R¹¹
G⁸

L_B182
R¹²
G⁸

L_B183
R¹³
G⁸

L_B184
R¹⁴
G⁸

L_B185
R¹⁵
G⁸

L_B186
R¹⁶
G⁸

L_B187
R¹⁷
G⁸

L_B188
R¹⁸
G⁸

L_B189
R¹⁹
G⁸

L_B190
R²⁰
G⁸

L_B191
R¹¹
G¹⁰

L_B192
R¹²
G¹⁰

L_B193
R¹³
G¹⁰

L_B194
R¹⁴
G¹⁰

L_B195
R¹⁵
G¹⁰

L_B196
R¹⁶
G¹⁰

L_B197
R¹⁷
G¹⁰

L_B198
R¹⁸
G¹⁰

L_B199
R¹⁹
G¹⁰

L_B200
R²⁰
G¹⁰

wherein R^Ehas the following structures:

[Image Omitted]

wherein G¹to G¹⁰have the following structures:

[Image Omitted]

In some embodiments, the compound is selected from the group consisting of Ir(L_A1)(L_B1-1)₂to Ir(L_A3241135)(L_B200-44)₂based on the general formula of Ir(L_AQ)(L_Bm-n)₂, wherein each L_AQand L_Bm-nis as defined above.

The present disclosure also discloses a method of preparing a complex compound of

[Image Omitted]

where the method comprises: reacting a compound of

[Image Omitted]

with a compound of

[Image Omitted]

in an organic solvent to produce the complex compound of Formula II; wherein,

- Y is O or S;
- L_Band L_Care each a bidentate monoanionic ligand;
- L_Band L_Care each the same or different, and can be linked to form a tetradentate ligand;
- R^Xis selected from the group consisting of alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroryl, vinyl, carboxylate, and combinations thereof;
- R^Yis selected from the group consisting of hydrogen, alkyl, heterolkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and combinations thereof; and
- R^Zis selected from the group consisting of alkyl, heterolkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and combinations thereof.

In the method, the organic solvent can be benzene or a substituted benzene. In some embodiments of the method, the reaction is carried out at a temperature equal to or greater than 100° C. In some embodiments of the method, R^Xis selected from the group consisting of carboxylate, alkyl, aryl, and vinyl. In some embodiments, R^Yis hydrogen or alkyl. In some embodiments, R^Zis alkyl or aryl. In some embodiments, L_Band L_Care each independently selected from the group consisting of:

[Image Omitted]

where each Y¹to Y¹³is independently selected from the group consisting of carbon and nitrogen; Y′ is selected from the group consisting of BR_e, NR_e, PR_e, O, S, Se, C═O, S═O, SO₂, CR_eR_f, SiR_eR_f, and GeR_eR_f; R_eand R_fcan be fused or joined to form a ring; each R_a, R_b, R_c, and R_dcan independently represent from mono to the maximum possible number of substitutions, or no substitution; each R_a, R_b, R_c, R_d, R_eand R_fis independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein; and any two adjacent substituents of R_a, R_b, R_c, and R_dcan be fused or joined to form a ring or form a multidentate ligand where chemically feasible.

In some embodiments of the method, L_Band L_Care each independently selected from the group consisting of:

[Image Omitted]

where: R_a′, R_b′, and R_c′ each independently represent zero, mono, or up to a maximum allowed substitution to its associated ring; each of R_a, R_b, R_c, R_N, R_a′, R_b′, and R_c′ is independently hydrogen or selected from a general substituent as described above; and two adjacent substituents of R_a′, R_b′, and R_c′ can be fused or joined to form a ring or form a multidentate ligand.

In some embodiments, the method further comprises purifying the complex compound of Formula II.

The present disclosure also provides a method of preparing a complex compound of

[Image Omitted]

where the method comprises: reacting a compound of

[Image Omitted]

with a compound of

[Image Omitted]

in an organic solvent to produce the complex compound of Formula V; where, R, R^Aand R^Bare each independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein; two substituents can be joined to form a fused ring; R₁is selected from the group consisting of alkyl, aryl, and OR; R₂is selected from the group consisting of alkyl and aryl; and R₃is selected from the group consisting of alkyl, aryl, and H. In the method, the organic solvent can be benzene or a substituted benzene. In some embodiments, the method further comprises purifying the produced complex compound of Formula V.

The present disclosure also provides a method of preparing a complex compound of

[Image Omitted]

where the method comprises: reacting a compound of

[Image Omitted]

with a compound of

[Image Omitted]

in an organic solvent to produce the complex compound of Formula VIII, where: Y is selected from the group consisting of OH and SH; R, R^Aand R^Bare each independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein, where two substituents can be joined to form a fused ring; R₁is selected from the group consisting of alkyl, aryl, and OR; and R₂is selected from the group consisting of alkyl and aryl. In some embodiments of the method, the organic solvent can be benzene or a substituted benzene. In some embodiments, the method further comprises purifying the produced compound of Formula VIII.

C. The OLEDs and the Devices of the Present Disclosure

In another aspect, the present disclosure also provides an OLED device comprising a first organic layer that contains a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the first organic layer comprises a compound comprising a first ligand L_Aof

[Image Omitted]

where: R^A, R^B, and R^Care each independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein; two of R^A, R^B, and R^Care independently NRR′, OR, SR, or CO₂R, but R^Aand R^Bcannot be concurrently OR; R and R′ are each independently alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, aryl, heteroaryl, silyl, or combinations thereof; two substituents can be joined or fused to form a ring, L_Ais coordinated to a metal M selected from the group consisting of Re, Ru, Os, Rh, Ir, Pd, Pt, Cu, Ag, and Cu; and the metal M is coordinated to additional maximum allowable number of ligands.

In some embodiments of the OLED, the organic layer is an emissive layer and the compound can be an emissive dopant or a non-emissive dopant. In some embodiments of the OLED, the compound is a fluorescent emitter.

In some embodiments of the OLED, the organic layer further comprises a host, wherein host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene. In some embodiments, the host is selected from the group consisting of the HOST Group defined herein.

In some embodiments of the OLED, the organic layer further comprises a host that comprises a metal complex.

In some embodiments, the organic layer may be an emissive layer and the compound as described herein may be an emissive dopant or a non-emissive dopant.

In some embodiments, the organic layer may further comprise a host, wherein the host comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan, wherein any substituent in the host is an unfused substituent independently selected from the group consisting of C_nH_2n+1, OC_nH_2n+1, OAr₁, N(C_nH_2n+1)₂, N(Ar₁)(Ar₂), CH═CH—C_nH_2n+1, C≡CC_nH_2n+1, Ar₁, Ar₁—Ar₂, C_nH_2n—Ar₁, or no substitution, wherein n is from 1 to 10; and wherein Ar₁and Ar₂are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.

In some embodiments, the organic layer may further comprise a host, wherein host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.

In some embodiments, the host may be selected from the HOST Group consisting of:

[Image Omitted]

and combinations thereof.

In some embodiments, the organic layer may further comprise a host, wherein the host comprises a metal complex.

In some embodiments, the compound as described herein may be a sensitizer; wherein the device may further comprise an acceptor; and wherein the acceptor may be selected from the group consisting of fluorescent emitter, delayed fluorescence emitter, and combination thereof.

In yet another aspect, the OLED of the present disclosure may also comprise an emissive region containing a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the emissive region comprises a compound comprising a first ligand L_Aof

[Image Omitted]

wherein: R^A, R^B, and R^Care each independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein; two of R^A, R^B, and R^Care independently NRR′, OR, SR, or CO₂R, but R^Aand R^Bcannot be concurrently OR: R and R′ are each independently alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, aryl, heteroaryl, silyl, or combinations thereof; two substituents can be joined or fused to form a ring, L_Ais coordinated to a metal M selected from the group consisting of Re, Ru, Os, Rh, Ir, Pd, Pt, Cu, Ag, and Cu; and the metal M is coordinated to additional maximum allowable number of ligands.

In yet another aspect, the present disclosure also provides a consumer product comprising an organic light-emitting device (OLED) having an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer may comprise a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the consumer product comprises an organic light-emitting device (OLED) having an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer may comprises a compound comprising a first ligand L_Aof

[Image Omitted]

wherein: R^A, R^B, and R^Care each independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein; two of R^A, R^B, and R^Care independently NRR′, OR, SR, or CO₂R, but R^Aand R^Bcannot be concurrently OR; R and R′ are each independently alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, aryl, heteroaryl, silyl, or combinations thereof; two substituents can be joined or fused to form a ring, L_Ais coordinated to a metal M selected from the group consisting of Re, Ru, Os, Rh, Ir, Pd, Pt, Cu, Ag, and Cu; and the metal M is coordinated to additional maximum allowable number of ligands.

In some embodiments, the consumer product can be one of a flat panel display, a computer monitor, a medical monitor, a television, a billboard, a light for interior or exterior illumination and/or signaling, a heads-up display, a fully or partially transparent display, a flexible display, a laser printer, a telephone, a cell phone, tablet, a phablet, a personal digital assistant (PDA), a wearable device, a laptop computer, a digital camera, a camcorder, a viewfinder, a micro-display that is less than 2 inches diagonal, a 3-D display, a virtual reality or augmented reality display, a vehicle, a video wall comprising multiple displays tiled together, a theater or stadium screen, a light therapy device, and a sign.

Generally, an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode. When a current is applied, the anode injects holes and the cathode injects electrons into the organic layer(s). The injected holes and electrons each migrate toward the oppositely charged electrode. When an electron and hole localize on the same molecule, an “exciton,” which is a localized electron-hole pair having an excited energy state, is formed. Light is emitted when the exciton relaxes via a photoemissive mechanism. In some cases, the exciton may be localized on an excimer or an exciplex. Non-radiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.

Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.

The initial OLEDs used emissive molecules that emitted light from their singlet states (“fluorescence”) as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.

More recently, OLEDs having emissive materials that emit light from triplet states (“phosphorescence”) have been demonstrated. Baldo et al., “Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices,” Nature, vol. 395, 151-154, 1998; (“Baldo-I”) and Baldo et al., “Very high-efficiency green organic light-emitting devices based on electrophosphorescence,” Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999) (“Baldo-II”), are incorporated by reference in their entireties. Phosphorescence is described in more detail in U.S. Pat. No. 7,279,704 at cols. 5-6, which are incorporated by reference.

FIG. 1 shows an organic light emitting device 100. The figures are not necessarily drawn to scale. Device 100 may include a substrate 110, an anode 115, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, a cathode 160, and a barrier layer 170. Cathode 160 is a compound cathode having a first conductive layer 162 and a second conductive layer 164. Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in U.S. Pat. No. 7,279,704 at cols. 6-10, which are incorporated by reference.

More examples for each of these layers are available. For example, a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety. An example of a p-doped hole transport layer is m-MTDATA doped with F₄-TCNQ at a molar ratio of 50:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which is incorporated by reference in its entirety. An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entireties, disclose examples of cathodes including compound cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electrically-conductive, sputter-deposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Patent Application Publication No. 2003/0230980, which are incorporated by reference in their entireties. Examples of injection layers are provided in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of protective layers may be found in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety.

FIG. 2 shows an inverted OLED 200. The device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230. Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an “inverted” OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200. FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.

The simple layered structure illustrated in FIGS. 1 and 2 is provided by way of non-limiting example, and it is understood that embodiments of the present disclosure may be used in connection with a wide variety of other structures. The specific materials and structures described are exemplary in nature, and other materials and structures may be used. Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used. Also, the layers may have various sublayers. The names given to the various layers herein are not intended to be strictly limiting. For example, in device 200, hole transport layer 225 transports holes and injects holes into emissive layer 220, and may be described as a hole transport layer or a hole injection layer. In one embodiment, an OLED may be described as having an “organic layer” disposed between a cathode and an anode. This organic layer may comprise a single layer, or may further comprise multiple layers of different organic materials as described, for example, with respect to FIGS. 1 and 2.

Structures and materials not specifically described may also be used, such as OLEDs comprised of polymeric materials (PLEDs) such as disclosed in U.S. Pat. No. 5,247,190 to Friend et al., which is incorporated by reference in its entirety. By way of further example. OLEDs having a single organic layer may be used. OLEDs may be stacked, for example as described in U.S. Pat. No. 5,707,745 to Forrest et al, which is incorporated by reference in its entirety. The OLED structure may deviate from the simple layered structure illustrated in FIGS. 1 and 2. For example, the substrate may include an angled reflective surface to improve out-coupling, such as a mesa structure as described in U.S. Pat. No. 6,091,195 to Forrest et al., and/or a pit structure as described in U.S. Pat. No. 5,834,893 to Bulovic et al., which are incorporated by reference in their entireties.

Unless otherwise specified, any of the layers of the various embodiments may be deposited by any suitable method. For the organic layers, preferred methods include thermal evaporation, ink-jet, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102 to Forrest et al., which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. Pat. No. 7,431,968, which is incorporated by reference in its entirety. Other suitable deposition methods include spin coating and other solution based processes. Solution based processes are preferably carried out in nitrogen or an inert atmosphere. For the other layers, preferred methods include thermal evaporation. Preferred patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as ink-jet and organic vapor jet printing (OVJP). Other methods may also be used. The materials to be deposited may be modified to make them compatible with a particular deposition method. For example, substituents such as alkyl and aryl groups, branched or unbranched, and preferably containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having 20 carbons or more may be used, and 3-20 carbons are a preferred range. Materials with asymmetric structures may have better solution processability than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize. Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.

Devices fabricated in accordance with embodiments of the present disclosure may further optionally comprise a barrier layer. One purpose of the barrier layer is to protect the electrodes and organic layers from damaging exposure to harmful species in the environment including moisture, vapor and/or gases, etc. The barrier layer may be deposited over, under or next to a substrate, an electrode, or over any other parts of a device including an edge. The barrier layer may comprise a single layer, or multiple layers. The barrier layer may be formed by various known chemical vapor deposition techniques and may include compositions having a single phase as well as compositions having multiple phases. Any suitable material or combination of materials may be used for the barrier layer. The barrier layer may incorporate an inorganic or an organic compound or both. The preferred barrier layer comprises a mixture of a polymeric material and a non-polymeric material as described in U.S. Pat. No. 7,968,146, PCT Pat. Application Nos. PCT/US2007/023098 and PCT/US2009/042829, which are herein incorporated by reference in their entireties. To be considered a “mixture”, the aforesaid polymeric and non-polymeric materials comprising the barrier layer should be deposited under the same reaction conditions and/or at the same time. The weight ratio of polymeric to non-polymeric material may be in the range of 95:5 to 5:95. The polymeric material and the non-polymeric material may be created from the same precursor material. In one example, the mixture of a polymeric material and a non-polymeric material consists essentially of polymeric silicon and inorganic silicon.

Devices fabricated in accordance with embodiments of the present disclosure can be incorporated into a wide variety of electronic component modules (or units) that can be incorporated into a variety of electronic products or intermediate components. Examples of such electronic products or intermediate components include display screens, lighting devices such as discrete light source devices or lighting panels, etc. that can be utilized by the end-user product manufacturers. Such electronic component modules can optionally include the driving electronics and/or power source(s). Devices fabricated in accordance with embodiments of the present disclosure can be incorporated into a wide variety of consumer products that have one or more of the electronic component modules (or units) incorporated therein. A consumer product comprising an OLED that includes the compound of the present disclosure in the organic layer in the OLED is disclosed. Such consumer products would include any kind of products that include one or more light source(s) and/or one or more of some type of visual displays. Some examples of such consumer products include flat panel displays, curved displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, rollable displays, foldable displays, stretchable displays, laser printers, telephones, mobile phones, tablets, phablets, personal digital assistants (PDAs), wearable devices, laptop computers, digital cameras, camcorders, viewfinders, micro-displays (displays that are less than 2 inches diagonal), 3-D displays, virtual reality or augmented reality displays, vehicles, video walls comprising multiple displays tiled together, theater or stadium screen, a light therapy device, and a sign. Various control mechanisms may be used to control devices fabricated in accordance with the present disclosure, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18degrees C. to 30 degrees C., and more preferably at room temperature (20-25° C.), but could be used outside this temperature range, for example, from −40 degree C. to +80° C.

More details on OLEDs, and the definitions described above, can be found in U.S. Pat. No. 7,279,704, which is incorporated herein by reference in its entirety.

The materials and structures described herein may have applications in devices other than OLEDs. For example, other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures. More generally, organic devices, such as organic transistors, may employ the materials and structures.

In some embodiments, the OLED has one or more characteristics selected from the group consisting of being flexible, being rollable, being foldable, being stretchable, and being curved. In some embodiments, the OLED is transparent or semi-transparent. In some embodiments, the OLED further comprises a layer comprising carbon nanotubes.

In some embodiments, the OLED further comprises a layer comprising a delayed fluorescent emitter. In some embodiments, the OLED comprises a RGB pixel arrangement or white plus color filter pixel arrangement. In some embodiments, the OLED is a mobile device, a hand held device, or a wearable device. In some embodiments, the OLED is a display panel having less than 10 inch diagonal or 50 square inch area. In some embodiments, the OLED is a display panel having at least 10 inch diagonal or 50 square inch area. In some embodiments, the OLED is a lighting panel.

In some embodiments, the compound can be an emissive dopant. In some embodiments, the compound can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence; see, e.g., U.S. application Ser. No. 15/700,352, which is hereby incorporated by reference in its entirety), triplet-triplet annihilation, or combinations of these processes. In some embodiments, the emissive dopant can be a racemic mixture, or can be enriched in one enantiomer. In some embodiments, the compound can be homoleptic (each ligand is the same). In some embodiments, the compound can be heteroleptic (at least one ligand is different from others). When there are more than one ligand coordinated to a metal, the ligands can all be the same in some embodiments. In some other embodiments, at least one ligand is different from the other ligands. In some embodiments, every ligand can be different from each other. This is also true in embodiments where a ligand being coordinated to a metal can be linked with other ligands being coordinated to that metal to form a tridentate, tetradentate, pentadentate, or hexadentate ligands. Thus, where the coordinating ligands are being linked together, all of the ligands can be the same in some embodiments, and at least one of the ligands being linked can be different from the other ligand(s) in some other embodiments.

In some embodiments, the compound can be used as a phosphorescent sensitizer in an OLED where one or multiple layers in the OLED contains an acceptor in the form of one or more fluorescent and/or delayed fluorescence emitters. In some embodiments, the compound can be used as one component of an exciplex to be used as a sensitizer. As a phosphorescent sensitizer, the compound must be capable of energy transfer to the acceptor and the acceptor will emit the energy or further transfer energy to a final emitter. The acceptor concentrations can range from 0.001% to 100%. The acceptor could be in either the same layer as the phosphorescent sensitizer or in one or more different layers. In some embodiments, the acceptor is a TADF emitter. In some embodiments, the acceptor is a fluorescent emitter. In some embodiments, the emission can arise from any or all of the sensitizer, acceptor, and final emitter.

According to another aspect, a formulation comprising the compound described herein is also disclosed.

The OLED disclosed herein can be incorporated into one or more of a consumer product, an electronic component module, and a lighting panel. The organic layer can be an emissive layer and the compound can be an emissive dopant in some embodiments, while the compound can be a non-emissive dopant in other embodiments.

In yet another aspect of the present disclosure, a formulation that comprises the novel compound disclosed herein is described. The formulation can include one or more components selected from the group consisting of a solvent, a host, a hole injection material, hole transport material, electron blocking material, hole blocking material, and an electron transport material, disclosed herein.

The present disclosure encompasses any chemical structure comprising the novel compound of the present disclosure, or a monovalent or polyvalent variant thereof. In other words, the inventive compound, or a monovalent or polyvalent variant thereof, can be a part of a larger chemical structure. Such chemical structure can be selected from the group consisting of a monomer, a polymer, a macromolecule, and a supramolecule (also known as supermolecule). As used herein, a “monovalent variant of a compound” refers to a moiety that is identical to the compound except that one hydrogen has been removed and replaced with a bond to the rest of the chemical structure. As used herein, a “polyvalent variant of a compound” refers to a moiety that is identical to the compound except that more than one hydrogen has been removed and replaced with a bond or bonds to the rest of the chemical structure. In the instance of a supramolecule, the inventive compound can also be incorporated into the supramolecule complex without covalent bonds.

D. Combination of the Compounds of the Present Disclosure with Other Materials

The materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device. For example, emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present. The materials described or referred to below are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.

a) Conductivity Dopants:

A charge transport layer can be doped with conductivity dopants to substantially alter its density of charge carriers, which will in turn alter its conductivity. The conductivity is increased by generating charge carriers in the matrix material, and depending on the type of dopant, a change in the Fermi level of the semiconductor may also be achieved. Hole-transporting layer can be doped by p-type conductivity dopants and n-type conductivity dopants are used in the electron-transporting layer.

Non-limiting examples of the conductivity dopants that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP01617493, EP01968131, EP2020694, EP2684932, US20050139810, US20070160905,US20090167167, US2010288362, WO06081780, WO2009003455, WO2009008277, WO2009011327.WO2014009310, US2007252140, US2015060804, US20150123047, and US2012146012.

[Image Omitted]

b) HIL/HTL:

A hole injecting/transporting material to be used in the present disclosure is not particularly limited, and any compound may be used as long as the compound is typically used as a hole injecting/transporting material. Examples of the material include, but are not limited to: a phthalocyanine or porphyrin derivative; an aromatic amine derivative; an indolocarbazole derivative; a polymer containing fluorohydrocarbon; a polymer with conductivity dopants; a conducting polymer, such as PEDOT/PSS; a self-assembly monomer derived from compounds such as phosphonic acid and silane derivatives; a metal oxide derivative, such as MoO_x; a p-type semiconducting organic compound, such as 1,4,5,8,9,12-Hexaazatriphenylenehexacarbonitrile; a metal complex, and a cross-linkable compounds.

Examples of aromatic amine derivatives used in HIL or HTL include, but not limit to the following general structures:

[Image Omitted]

Each of Ar¹to Ar⁹is selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each Ar may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, Ar¹to Ar⁹is independently selected from the group consisting of:

[Image Omitted]

wherein k is an integer from 1 to 20; X¹⁰¹to X¹⁰⁸is C (including CH) or N; Z¹⁰¹is NAr¹, O, or S; Ar¹has the same group defined above.

Examples of metal complexes used in HIL or HTL include, but are not limited to the following general formula:

[Image Omitted]

wherein Met is a metal, which can have an atomic weight greater than 40; (Y¹⁰¹-Y¹⁰²) is a bidentate ligand, Y¹⁰¹and Y¹⁰²are independently selected from C, N, O, P, and S; L¹⁰¹is an ancillary ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.

In one aspect, (Y¹⁰¹-Y¹⁰²) is a 2-phenylpyridine derivative. In another aspect, (Y¹⁰¹-Y¹⁰²) is a carbene ligand. In another aspect, Met is selected from Ir, Pt, Os, and Zn. In a further aspect, the metal complex has a smallest oxidation potential in solution vs. Fc⁺/Fc couple less than about 0.6 V.

Non-limiting examples of the HIL and HTL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN102702075, DE102012005215, EP01624500, EP01698613, EP01806334, EP01930964, EP01972613, EP01997799, EP02011790, EP02055700, EP02055701, EP1725079, EP2085382, EP2660300, EP650955, JP07-073529, JP2005112765, JP2007091719, JP2008021687, JP2014-009196, KR20110088898, KR20130077473, TW201139402, U.S. Ser. No. 06/517,957, US20020158242, US20030162053, US20050123751, US20060182993, US20060240279, US20070145888, US20070181874, US20070278938, US20080014464, US20080091025, US20080106190, US20080124572, US20080145707, US20080220265, US20080233434, US20080303417, US2008107919, US20090115320, US20090167161, US2009066235, US2011007385, US20110163302, US2011240968, US2011278551, US2012205642, US2013241401, US20140117329, US2014183517, U.S. Pat. Nos. 5,061,569, 5,639,914, WO05075451, WO07125714, WO08023550, WO08023759, WO2009145016, WO2010061824, WO2011075644, WO2012177006, WO2013018530, WO2013039073, WO2013087142, WO2013118812, WO2013120577, WO2013157367, WO2013175747, WO2014002873, WO2014015935, WO2014015937, WO2014030872, WO2014030921, WO2014034791, WO2014104514, WO2014157018.

[Image Omitted]

c) EBL:

An electron blocking layer (EBL) may be used to reduce the number of electrons and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies, and/or longer lifetime, as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than the emitter closest to the EBL interface. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than one or more of the hosts closest to the EBL interface. In one aspect, the compound used in EBL contains the same molecule or the same functional groups used as one of the hosts described below.

d) Hosts:

The light emitting layer of the organic EL device of the present disclosure preferably contains at least a metal complex as light emitting material, and may contain a host material using the metal complex as a dopant material. Examples of the host material are not particularly limited, and any metal complexes or organic compounds may be used as long as the triplet energy of the host is larger than that of the dopant. Any host material may be used with any dopant so long as the triplet criteria is satisfied.

Examples of metal complexes used as host are preferred to have the following general formula:

[Image Omitted]

wherein Met is a metal; (Y¹⁰³-Y¹⁰⁴) is a bidentate ligand, Y¹⁰³and Y¹⁰⁴are independently selected from C, N, O, P, and S; L¹⁰¹is an another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal. In another aspect, Met is selected from Ir and Pt. In a further aspect, (Y¹⁰³-Y¹⁰⁴) is a carbene ligand.

In one aspect, the metal complexes are:

[Image Omitted]

wherein (O—N) is a bidentate ligand, having metal coordinated to atoms O and N.

In one aspect, the host compound contains at least one of the following groups selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each option within each group may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, the host compound contains at least one of the following groups in the molecule:

[Image Omitted]

wherein R¹⁰¹is selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and when it is aryl or heteroaryl, it has the similar definition as Ar's mentioned above. k is an integer from 0 to 20 or 1 to 20. X¹⁰¹to X¹⁰⁸are independently selected from C (including CH) or N. Z¹⁰¹and Z¹⁰²are independently selected from NR¹⁰¹, O, or S.

Non-limiting examples of the host materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP2034538, EP2034538A, EP2757608, JP2007254297, KR20100079458, KR20120088644, KR20120129733, KR20130115564, TW201329200, US20030175553, US20050238919, US20060280965, US20090017330, US20090030202, US20090167162, US20090302743, US20090309488, US20100012931, US20100084966, US20100187984, US2010187984, US2012075273, US2012126221, US2013009543, US2013105787, US2013175519, US2014001446, US20140183503, US20140225088, US2014034914, U.S. Pat. No. 7,154,114, WO2001039234, WO2004093207, WO2005014551, WO2005089025, WO2006072002, WO2006114966, WO2007063754, WO2008056746, WO2009003898, WO2009021126, WO2009063833, WO2009066778, WO2009066779, WO2009086028, WO2010056066, WO2010107244, WO2011081423, WO2011081431, WO2011086863, WO2012128298, WO2012133644, WO2012133649, WO2013024872, WO2013035275, WO2013081315, WO2013191404, WO2014142472, US20170263869, US20160163995, U.S. Pat. No. 9,466,803,

[Image Omitted]

e) Additional Emitters:

One or more additional emitter dopants may be used in conjunction with the compound of the present disclosure. Examples of the additional emitter dopants are not particularly limited, and any compounds may be used as long as the compounds are typically used as emitter materials. Examples of suitable emitter materials include, but are not limited to, compounds which can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence), triplet-triplet annihilation, or combinations of these processes.

Non-limiting examples of the emitter materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103694277, CN1696137, EB01238981, EP01239526, EP01961743, EP1239526, EP1244155, EP1642951, EP1647554, EP1841834, EP1841834B, EP2062907, EP2730583, JP2012074444, JP2013110263, JP4478555, KR1020090133652, KR20120032054, KR20130043460, TW201332980, U.S. Ser. No. 06/699,599, U.S. Ser. No. 06/916,554, US20010019782, US20020034656, US20030068526, US20030072964, US20030138657, US20050123788, US20050244673, US2005123791, US2005260449, US20060008670, US20060065890, US20060127696, US20060134459, US20060134462, US20060202194, US20060251923, US20070034863, US20070087321, US20070103060, US20070111026, US20070190359, US20070231600, US2007034863, US2007104979, US2007104980, US2007138437, US2007224450, US2007278936, US20080020237, US20080233410, US20080261076, US20080297033, US200805851, US2008161567, US2008210930, US20090039776, US20090108737, US20090115322, US20090179555, US2009085476, US2009104472, US20100090591, US20100148663, US20100244004, US20100295032, US2010102716, US2010105902, US2010244004, US2010270916, US20110057559, US20110108822, US20110204333, US2011215710, US2011227049, US2011285275, US2012292601, US20130146848, US2013033172, US2013165653, US2013181190, US2013334521, US20140246656, US2014103305, U.S. Pat. Nos. 6,303,238, 6,413,656, 6,653,654, 6,670,645, 6,687,266, 6,835,469, 6,921,915, 7,279,704, 7,332,232, 7,378,162, 7,534,505, 7,675,228, 7,728,137, 7,740,957, 7,759,489, 7,951,947, 8,067,099, 8,592,586, 8,871,361, WO06081973, WO06121811, WO07018067, WO07108362, WO07115970, WO07115981, WO08035571, WO2002015645, WO2003040257, WO2005019373, WO2006056418, WO2008054584, WO2008078800, WO2008096609, WO2008101842, WO2009000673, WO2009050281, WO2009100991, WO2010028151, WO2010054731, WO2010086089, WO2010118029, WO2011044988, WO2011051404, WO2011107491, WO2012020327, WO2012163471, WO2013094620, WO2013107487, WO2013174471, WO2014007565, WO2014008982, WO2014023377, WO2014024131, WO2014031977, WO2014038456, WO2014112450.

[Image Omitted]

f) HBL:

A hole blocking layer (HBL) may be used to reduce the number of holes and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies and/or longer lifetime as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and/or higher triplet energy than the emitter closest to the HBL interface. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and/or higher triplet energy than one or more of the hosts closest to the HBL interface.

In one aspect, compound used in HBL contains the same molecule or the same functional groups used as host described above.

In another aspect, compound used in HBL contains at least one of the following groups in the molecule:

[Image Omitted]

wherein k is an integer from 1 to 20; L¹⁰¹is another ligand, k′ is an integer from 1 to 3.

g) ETL:

Electron transport layer (ETL) may include a material capable of transporting electrons. Electron transport layer may be intrinsic (undoped), or doped. Doping may be used to enhance conductivity. Examples of the ETL material are not particularly limited, and any metal complexes or organic compounds may be used as long as they are typically used to transport electrons.

In one aspect, compound used in ETL contains at least one of the following groups in the molecule:

[Image Omitted]

wherein R¹⁰¹is selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, when it is aryl or heteroaryl, it has the similar definition as Ar's mentioned above. Ar¹to Ar³has the similar definition as Ar's mentioned above. k is an integer from 1 to 20. X¹⁰¹to X¹⁰⁸is selected from C (including CH) or N.

In another aspect, the metal complexes used in ETL contains, but not limit to the following general formula:

[Image Omitted]

wherein (O—N) or (N—N) is a bidentate ligand, having metal coordinated to atoms O, N or N, N; L¹⁰¹is another ligand: k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal.

Non-limiting examples of the ETL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103508940, EP01602648, EP01734038, EP01956007, JP2004-022334, JP2005149918, JP2005-268199, KR0117693, KR20130108183, US20040036077, US20070104977, US2007018155, US20090101870, US20090115316, US20090140637, US20090179554, US2009218940, US2010108990, US2011156017, US2011210320, US2012193612, US2012214993, US2014014925, US2014014927, US20140284580, U.S. Pat. Nos. 6,656,612, 8,415,031, WO2003060956, WO2007111263, WO2009148269, WO2010067894, WO2010072300, WO2011074770, WO2011105373, WO2013079217, WO2013145667, WO2013180376, WO2014104499, WO2014104535,

[Image Omitted]

h) Charge Generation Layer (CGL)

In tandem or stacked OLEDs, the CGL plays an essential role in the performance, which is composed of an n-doped layer and a p-doped layer for injection of electrons and holes, respectively. Electrons and holes are supplied from the CGL and electrodes. The consumed electrons and holes in the CGL are refilled by the electrons and holes injected from the cathode and anode, respectively; then, the bipolar currents reach a steady state gradually. Typical CGL materials include n and p conductivity dopants used in the transport layers.

In any above-mentioned compounds used in each layer of the OLED device, the hydrogen atoms can be partially or fully deuterated. Thus, any specifically listed substituent, such as, without limitation, methyl, phenyl, pyridyl, etc. may be undeuterated, partially deuterated, and fully deuterated versions thereof. Similarly, classes of substituents such as, without limitation, alkyl, aryl, cycloalkyl, heteroaryl, etc. also may be undeuterated, partially deuterated, and fully deuterated versions thereof.

D. Experimental Examples

General Information. All reactions were carried out with rigorous exclusion of air using Schlenk-tube techniques. Solvents (except MeOH which was dried and distilled under argon) were obtained oxygen-and water-free from an MBraun solvent purification apparatus High-resolution electrospray mass spectra were acquired using a MicroTOF-Q hybrid quadrupole time-of-flight spectrometer (Bruker Daltonics, Bremen, Germany). C, H, and N analyses were carried out in a Perkin-Elmer 2400 CHNS/O analyzer. ¹H and ¹³C{¹H} NMR spectra were recorded on a Bruker Avance 300 or 400 MHz instrument. Chemical shifts (expressed in parts per million) are referenced to residual solvent peaks. Coupling constants J are given in hertz.

Preparation of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(OMe)CHC(CO₂Me)O}

[Image Omitted]

A suspension of [Ir(μ-OH){κ²-C,N-(C₆H₄-isoqui)}₂]₂(800 mg, 0.647 mmol) in 10 mL of toluene was treated with dimethyl acetilenedicarboxylate (190 μL, 1.55 mmol) and the mixture was stirred under argon in a sealed tube at 120° C. for 24 hours. The resulting garnet solution was concentrated to ca. 1 mL and addition of MeOH (8 mL) caused the precipitation of a garnet solid, which was purified by silica column chromatography using dichloromethane/toluene 2:1 as eluent. Yield: 400 mg (41%). HRMS (electrospray, m/z): calculated for C₃₆H₂₇IrN₂NaO₅[M+Na]⁺: 783.1443; found 783.1427. Elemental analysis calcd (%) for C₃₆H₂₇IrN₂O₅: C 56.91; H 3.58; N 3.69. Found: C 56.99; H 3.55; N 4.04. X-ray- quality crystals were grown by layering a solution of this complex in toluene with MeOH. ¹H NMR (400.13 MHz, CD₂Cl₂, 298 K): δ 9.01 (m, 2H, isoqui), 8.53 (d, ³J_H-H=6.4, 1H NCH), 8.44 (d, ³J_H-H=6.3, 1H, NCH), 8.27 (m, 2H, C₆H₄), 8.00 (m, 2H, isoqui), 7.77 (m, 4H, isoqui), 7.58 (m, 2H, isoqui), 6.98 (m, 2H, C₆H₄), 6.70 (m, 2H, C₆H₄), 6.35 (m, 2H, C₆H₄), 5.59 (s, 1H, C(O)CHC(O)), 3.68 (s, 3H, CO₂Me), 3.44 (s, 3H, OMe). ¹³C{¹H} NMR (100.63 MHZ, CD₂Cl₂, 298 K): δ 170.9 (IrOC(OMe)), 169.2 (IrOC(CO₂Me)+C_qN), 168.8 (C_qN), 166.3 (CO₂Me), 150.1, 147.9 147.2, 146.9 (2C_qC₆H₄), 141.0, 140.7 (2 NCH), 137.9, 137.8 (2C_qisoqui), 134.0 (2CH C₆H₄), 131.4 (2CH isoqui), 130.2, 130.1, 129.4, 129.2 (4CH C₆H₄), 128.5, 128.4 (2CH isoqui), 127.8 (2CH isoqui), 127.0 (2CH isoqui), 126.8, 126.6 (2C_qisoqui), 121.3, 121.2 (2CH C₆H₄), 120.9 (2CH isoqui), 86.7 (C(O)CHC(O)), 52.8 (CO₂Me), 52.2 (IrOC(OMe). FIG. 3 shows the X-Ray diffraction analysis molecular diagram of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(OMe)CHC(CO₂Me)O}.

Preparation of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(Ph)CHC(OMe)O}

[Image Omitted]

A suspension of [Ir(μ-OH){κ²-C,N-(C₆H₄-isoqui)}₂]₂(250 mg, 0.202 mmol) in 5 mL of toluene was treated with methyl 3-phenylpropiolate (71.6 μL, 0.485 mmol) and the mixture was stirred under argon in a sealed tube at 120° C. for 36 h. The resulting garnet solution was concentrated to ca. 1 mL and addition of MeOH (8 mL) caused the precipitation of a garnet solid, which was purified by silica column chromatography using toluene/hexane 2:1 as eluent. Yield: (20 mg) 6%. HRMS (electrospray, m/z): calcd for C₄₀H₂₉IrN₂NaO₃[M+Na]⁺: 801.1726; found 801.1749. ¹H NMR (300 MHZ, CD₂Cl₂, 298 K): δ 9.03 (m, 2H), 8.57 (m, 2H), 8.28 (m, 2H), 7.96 (m, 2H), 7.75 (m, 4H), 7.63-7.47 (m, 4H), 7.36-7.17 (m, 3H), 6.97 (m, 2H), 6.70 (m, 2H), 6.44 (m, 2H), 5.36 (s, 1H, C(O)CHC(O)), 3.44 (s, 3H, OMe). ¹³C{¹H} NMR (75 MHZ, CD₂Cl₂, 298 K): δ 181.1 (OC(Ph)), 170.6 (OC(OMe)), 169.5, 169.0, 152.0, 149.7, 147.4, 147.0, 142.0 (7C_q), 141.1, 140.9 (2CH), 137.8, 137.7 (2C_q), 134.2, 133.9, 131.3, 131.2 (4CH), 130.1 (2CH), 129.9, 129.2, 129.1 (3CH), 128.4 (2CH), 128.3, 128.2 (2CH), 127.8 (2CH), 127.0 (2CH), 126.8 (2CH), 126.7 (2C_q), 120.9 (2CH), 120.6 (2CH), 82.3 (C(O)CHC(O)), 51.74 (OMe).

Preparation of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(Me)CHC(CHCH₂)O}

[Image Omitted]

A suspension of [Ir(μ-OH){κ²-C,N-(C₆H₄-isoqui)}₂]₂(300 mg, 0.243 mmol) in methyl vinyl ketone (2.30 mL, 27.6 mmol) was stirred under argon in a sealed tube at 80° C. for 5 h. Toluene (8 mL) was added to the resulting garnet solution, which was transferred via cannula to a schlenk tube and then it was concentrated to ca. 1 mL. The addition of MeOH (5 mL) caused the precipitation of a garnet solid, which was purified by silica column chromatography using toluene/hexane 5:1 as eluent. Yield: 20 mg (6%). HRMS (electrospray, m/z): calcd for C₃₆H₂₆IrN₂NaO₂[M−H+Na]⁺: 734.1518 ; found 734.1664. X-ray-quality crystals were grown by layering a solution of this complex in toluene with MeOH. ¹H NMR (400 MHz, CD₂Cl₂, 298 K): δ 8.98 (m, 2H), 8.58 (d, ³J_H-H=6.4, 1H), 8.54 (d, ³J_H-H=6.4, 1H), 8.23 (m, 2H), 7.96 (m, 2H), 7.73 (m, 4H), 7.51 (d, ³J_H-H=6.4, 1H), 7.47 (d, ³J_H-H=6.4, 1H), 6.93 (m, 2H), 6.67 (m, 2H), 6.45 (dd, ³J_H-H=7.5, ⁴J_H-H=1.3, 1H), 6.35 (dd, ³J_H-H=7.5, ⁴J_H-H=1.3, 1H), 6.14 (dd, ³J_H-Htrans=17.1, ³J_H-Hcis=10.4, 1H=CH), 5.67 (dd, ³J_H-Htrans=17.1, ²J_H-Hgem=2.3, 1H=CH₂), 5.15 (dd, ³J_H-Hcis=10.4, ²J_H-Hgem=2.3, 1H=CH₂), 4.84 (s, 1H, C(O)CHC(O)), 1.84 (s, 3H, Me). ¹³C{¹H} NMR (100 MHZ, CD₂Cl₂, 298 K): δ 170.5 (C_q), 169.1 (OC(CH═CH₂)), 168.6 (C_q), 164.1 (OC(Me)), 161.7, 154.3, 147.4, 147.1 (4C_q), 141.6, 141.0 (2CH), 140.3 (═CH), 137.5, 137.4 (2C_q), 133.9, 133.5, 131.0, 130.9, 130.2, 130.0, 129.2, 129.1, 128.1, 128.0, 127.8 (11CH), 127.5 (2CH), 126.9 (C_q), 126.8, 120.8, 120.7, 120.4, 120.2 (5CH), 118.0 (═CH₂), 98.1 (C(O)CHC(O)), 28.8 (Me). FIG. 4 shows X-Ray diffraction analysis molecular diagram of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(Me)CHC(CHCH₂)O}.

Preparation of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O-OC(Ph)CHC(p-C₆H₄Me)O}

[Image Omitted]

A suspension of [Ir(μ-OH){κ²-C,N-(C₆H₄-isoqui)}₂]₂(250 mg, 0.202 mmol) in 3- (4-methylphenyl)-1-phenylprop-2-en-1-one (675 mg, 3 mmol) was stirred under argon in a sealed tube at 100° C. for 36 h. The resulting garnet solution was dissolved in toluene (8 mL) to be cannulated to a schlenk tube and then, the solution was dried under vacuum. The resulting garnet oil was purified by silica column chromatography using toluene/hexane 1:1 as eluent. Yield: 20 mg (6%). HRMS (electrospray, m/z): calcd for C₄₆H₃₃IrN₂NaO₂[M+Na]⁺: 861.2067; found 861.2060. X-ray-quality crystals were grown by layering a solution of this complex in toluene with MeOH. ¹H NMR (300 MHZ, CD₂Cl₂, 298 K): 9.03 (m, 2H), 8.54 (m, 2H), 8.29 (m, 2H), 7.92 (m, 2H), 7.78-7.61 (m, 8H), 7.46 (m, 2H), 7.36 (m, 1H, Ph), 7.27 (m, 2H, Ph), 7.09 (m, 2H), 6.98 (m, 2H), 6.71 (m, 2H), 6.53 (s, 1H C(O)CHC(O)), 6.46 (m, 2H), 2.28 (s, 3H Me). ¹³C{¹H} NMR (75 MHZ, CD₂Cl₂, 298 K): δ 180.1, 179.9 (2CO), 169.4 (2C_qN), 152.3 (2C_q), 147.3 (2C_q), 142.0 (C_q^Me), 141.2 (C_q), 140.9 (2CH), 139.0 (C_q), 137.8 (2C_q), 134.2 (2CH), 131.2 (2CH), 130.5 (CH Ph), 130.2 (2CH), 129.3 (2CH), 129.2 (2CH), 128.6 (2CH), 128.2 (2CH), 127.8 (2CH), 127.1 (2CH), 127.0 (4CH), 126.8 (2C_q), 120.9 (2CH), 120.6 (2CH), 95.7 (CH C(O)CHC(O)), 21.5 (Me). FIG. 5 shows the X-Ray diffraction analysis molecular diagram of Ir{κ²-C,N-(C₆H₄-isoqui)}₂{κ²-O,O- OC(Ph)CHC(p-C₆H₄Me)O}.

A photoluminescence (PL) spectrum of the inventive compound Ir(L_B1-1)₂(L_A3241135) taken in PMMA film at room temperature is shown in FIG. 6. The PL intensity is normalized to the maximum of the emission peak. The peak maximum of the inventive example is 638 nm. The inventive example can be used as red emissive dopant in organic electroluminescence device.

It is understood that the various embodiments described herein are by way of example only and are not intended to limit the scope of the invention. For example, many of the materials and structures described herein may be substituted with other materials and structures without deviating from the spirit of the invention. The present invention as claimed may therefore include variations from the particular examples and preferred embodiments described herein, as will be apparent to one of skill in the art. It is understood that various theories as to why the invention works are not intended to be limiting.