JP2020189836A - Organic electroluminescent materials and devices - Google Patents

Abstract

To provide organometallic compounds and compositions and their various uses including as emitters in devices such as organic light-emitting diodes and related electronic devices.SOLUTION: There is provided a use of a specific platinum compound which can be prepared by following formula or the like.SELECTED DRAWING: Figure 1

Description

Cross-reference to related applications This application claims priority over US Provisional Application No. 62 / 850,800 filed May 21, 2019, pursuant to Article 119 (e) of the US Patent Act, and the disclosure of the contents. The whole is incorporated herein by reference.

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

Photoelectronic devices that utilize organic materials are becoming increasingly desirable for a variety of reasons. Since many of the materials used to make such devices are relatively inexpensive, organic optoelectronic devices have the potential for cost advantage over inorganic devices. In addition, the inherent properties of organic materials, such as flexibility, can make the material well suited for specific applications such as fabrication on flexible substrates. Examples of organic optoelectronic devices include organic light emitting diodes / devices (OLEDs), organic light transistors, organic photovoltaic cells and photodetectors. For OLEDs, organic materials can have performance advantages over conventional materials.

OLEDs utilize thin organic films that emit light when a voltage is applied to the entire device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, lighting and backlighting.

One use of phosphorescent luminescent molecules is in full color displays. Industry standards for such displays require pixels that are adapted to emit a particular color, called a "saturated" color. In particular, these standards require saturated red, green and blue pixels. Alternatively, the OLED can be designed to emit white light. Conventional LCD display emission from a white backlight is filtered using an absorption filter to produce red, green, and blue emission. Similar techniques can be used with OLEDs. The white OLED can be either a single light emitting layer (EML) device or a laminate structure. Color can be measured using CIE coordinates well known in the art.

A transition metal compound having a naphthylene-aryl bidentate ligand which is a rigid and conjugated moiety is disclosed. Such transition metal complexes are useful as illuminant materials in organic electroluminescence devices.

In one aspect, the present disclosure provides a compound comprising a first ligand L _A of formula 1.
Wherein each ^X 1 ^{to X 10} is C or N; maximum number of the N of ^X 1 ^{to X 10} in the same ring is an 3; ^{R A} and ^{R B,} respectively, from mono It represents the maximum acceptable substituted or unsubstituted a represents; L _a is complexed with the metal M; each R ^a and R ^B are independently hydrogen, or as defined herein a substituent selected from the group consisting of general substituents that; M may be coordinated with other ligands; the ligand L _a is combined with other ligands It can include tridentate, tetradentate, pentadentate, or hexadentate ligands; any two substituents can bond or condense with each other to form a ring.

In another aspect, the present disclosure provides compositions of the compounds of the present disclosure.

In yet another aspect, the present disclosure provides an OLED having an organic layer containing the compounds of the present disclosure.

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

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 photoluminescence (PL) spectrum of Example Compound I-A34 of the present invention obtained in a 2-methyl THF solution at room temperature.

A. Terms Unless otherwise specified, the following terms used herein are defined as follows:

As used herein, the term "organic" includes polymeric and low molecular weight organic materials that can be used to make organic optoelectronic devices. "Small molecule" refers to any organic material that is not a polymer, and "small molecule" may actually be quite large. Small molecules can contain repeating units in some situations. For example, using a long-chain alkyl group as a substituent does not exclude the molecule from the "small molecule" class. Small molecules may be incorporated into the polymer, for example as pendant groups on the polymer backbone or as part of the backbone. Small molecules can also serve as the core part of a dendrimer consisting of a series of chemical shells built on top of the core part. The core portion of the dendrimer may be a fluorescent or phosphorescent small molecule illuminant. Dendrimers can be "small molecules" and all dendrimers currently in use in the field of OLEDs are considered to be small molecules.

As used herein, "top" means the furthest part from the substrate, while "bottom" means the most recent part of the substrate. When the first layer is described as "located above" the second layer, the first layer is located farther from the substrate. There may be other layers between the first layer and the second layer, unless it is specified that the first layer is "in contact" with the second layer. For example, the cathode can be described as "located above" the anode, even though there are various organic layers in between.

As used herein, "solution processable" can be dissolved, dispersed or transported in a liquid medium, either in solution or suspension form, and / or deposited from that medium. It means that you can do it.

A ligand can be referred to as "photoactive" if the ligand is believed to directly contribute to the photoactive properties of the light emitting material. A ligand can be referred to as an "auxiliary" if it is believed that the ligand does not contribute to the photoactive properties of the light emitting material, whereas the co-ligand has the properties of a photoactive ligand Can be changed.

As used herein, the first "highest occupied molecular orbital" (HOMO) or "lowest empty molecular orbital" (LUMO) energy level is the first, as is generally understood by those skilled in the art. If the energy level of is close to the vacuum energy level, then the second HOMO or LUMO energy level is "greater than" or "higher". Since the ionization potential (IP) is measured as negative energy compared to the vacuum level, a higher HOMO energy level corresponds to an IP with a smaller absolute value (a less negative IP). Similarly, higher LUMO energy levels correspond to electron affinity (EA) (less negative EA) with a smaller absolute value. In a conventional energy level diagram with a vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. The "higher" HOMO or LUMO energy level appears to be closer to the top of such a figure than the "lower" HOMO or LUMO energy level.

As used herein, the first work function is greater than the second work function, as is generally understood by those skilled in the art, if the first work function has a higher absolute value. Or "higher than". This means that the "higher" work function is even more negative, as the work function is generally measured as a negative number compared to the vacuum level. In a traditional energy level diagram with a vacuum level at the top, the "higher" work function is illustrated as being far downward from the vacuum level. Therefore, the definitions of HOMO and LUMO energy levels follow a convention different from the work function.

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 group (C (O) -R _s ).

The term "ester" refers to a substituted oxycarbonyl (-OC (O) -R _s or -C (O) -OR _s ) group.

The term "ether" refers to the -OR _s group.

The terms "sulfanyl" or "thioether" are used interchangeably and refer to the -SR _s group.

The term "sulfinyl" refers to a -S (O) -R _s group.

The term "sulfonyl" refers to the -SO _2- R _s group.

The term "phosphino" refers to -P (R _{s) 3} group, each R _s may be be the same or different.

The term "silyl" refers to -Si _{(R s) 3} group, each _{R s} may be be the same or different.

The term "boryl" refers to _two -B (R _s ) or _three Lewis adducts-B (R _s ) thereof, where R _s may be the same or different.

In each of the above, R _s is hydrogen, or deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl , Alkinyl, aryl, heteroaryl, and substituents selected from the group consisting of combinations thereof. Preferred R _s is alkyl, cycloalkyl, aryl, heteroaryl, and is selected from the group consisting of.

The term "alkyl" refers to and includes both straight chain and branched chain alkyl groups. Preferred alkyl groups include from 1 to 15 carbon atoms and include methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, pentyl, 1-methylbutyl, and more. Examples thereof include 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, and 2,2-dimethylpropyl. Further, the alkyl group may be optionally substituted.

The term "cycloalkyl" refers to and includes monocyclic, polycyclic, and spiroalkyl groups. Preferred cycloalkyl groups are those containing 3 to 12 ring carbon atoms, such as cyclopropyl, cyclopentyl, cyclohexyl, bicyclo [3.1.1] heptyl, spiro [4.5] decyl, spiro [5.5]. ] Undecylic, Adamantyl, etc. can be mentioned. Further, the cycloalkyl group may be optionally substituted.

The terms "heteroalkyl" or "heterocycloalkyl" refer to alkyl or cycloalkyl groups having at least one carbon atom substituted with a heteroatom, respectively. Optionally, at least one heteroatom is selected from O, S, N, P, B, Si, and Se, preferably O, S, or N. Further, the heteroalkyl group or the heterocycloalkyl group may be optionally substituted.

The term "alkenyl" refers to and includes both straight-chain and branched-chain alkene groups. An alkenyl group is essentially an alkyl group containing at least one carbon-carbon double bond in the alkyl chain. A cycloalkenyl group is essentially a cycloalkyl group containing at least one carbon-carbon double bond in the cycloalkyl ring. As used herein, the term "heteroalkenyl" refers to an alkenyl group having at least one carbon atom substituted by a heteroatom. Optionally, 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 2 to 15 carbon atoms. Further, the alkenyl, the cycloalkenyl, or the heteroalkenyl group may be optionally substituted.

The term "alkynyl" refers to and includes both straight chain and branched alkyne groups. An alkynyl group is essentially an alkyl group containing at least one carbon-carbon triple bond in the alkyl chain. Preferred alkynyl groups are those containing 2 to 15 carbon atoms. Further, the alkynyl group may be optionally substituted.

The terms "aralkyl" or "arylalkyl" are used interchangeably and refer to alkyl groups substituted with aryl groups. Further, the aralkyl group may be optionally substituted.

The term "heterocyclic group" refers to and includes aromatic and non-aromatic cyclic groups 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. Heteroaromatic cyclic groups can be used interchangeably with heteroaryls. Preferred hetero-non-aromatic cyclic groups are those containing 3-7 ring atoms, including at least one hetero atom, cyclic amines such as morpholino, piperidino, pyrrolidino, and eg, tetrahydrofuran, tetrahydropyran, etc. Includes cyclic ethers / thioethers such as tetrahydrothiophene. Further, the heterocyclic group may be optionally substituted.

The term "aryl" refers to and includes both monocyclic aromatic hydrocarbyl groups and polycyclic aromatic ring systems. A polycycle can have two or more rings in which two carbons are shared by two adjacent rings (the rings are "condensed"), and at least one of the rings is It is an aromatic hydrocarbyl group, for example, the other ring can be cycloalkyl, cycloalkenyl, aryl, heterocycle, and / or heteroaryl. Preferred aryl groups include those containing 6 to 30 carbon atoms, preferably those containing 6 to 20 carbon atoms, and even more preferably those containing 6 to 12 carbon atoms. An aryl group having 6 carbons, an aryl group having 10 carbons, or an aryl group having 12 carbons is particularly preferable. Suitable aryl groups include phenyl, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenalene, fluorene, pyrene, chrysene, perylene, azulene and the like, and include phenyl, biphenyl, triphenyl, triphenylene and the like. , Fluorene, and naphthalene are preferred. Further, the aryl group may be optionally substituted.

The term "heteroaryl" refers to and includes both monocyclic aromatic groups and polycyclic aromatic ring systems containing at least one heteroatom. Heteroatoms include, but are not limited to, O, S, N, P, B, Si, and Se. In many examples, O, S, or N are the preferred heteroatoms. The heteromonocyclic aromatic system is preferably a monocycle having 5 or 6 ring atoms, and the ring can have 1 to 6 heteroatoms. A heteropolycyclic ring system can have two or more rings in which two atoms are common to two adjacent rings (the rings are "condensed"), and at least one of the rings. Is a heteroaryl, for example, the other ring can be a cycloalkyl, cycloalkenyl, aryl, heterocycle, and / or heteroaryl. The complex polycyclic aromatic ring system can have 1 to 6 heteroatoms per ring of the polycyclic aromatic ring system. Preferred heteroaryl groups include those containing 3 to 30 carbon atoms, preferably those containing 3 to 20 carbon atoms, and more preferably those containing 3 to 12 carbon atoms. Suitable heteroaryl groups include dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole. , Thiazol, Oxazole, Oxazole, Dioxazole, Thiasiazol, Pyridine, Pyridazine, Pyrimidine, Pyrazine, Triazine, Oxazole, Oxazole, Oxazole, Indole, Benzimidazole, Indazole, Indoxazine, Benxazole, Benzisooxazole, Benzothazole , Kinolin, isoquinolin, cinnoline, quinazoline, quinoxalin, naphthylidine, phthalazine, pteridine, xanthene, acrydin, phenazine, phenothiazine, phenoxazine, benzoflopyridine, flodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine. Dibenzothiophene, dibenzofuran, dibenzoselenophen, carbazole, indolocarbazole, imidazole, pyridine, triazine, benzimidazole, 1,2-azaborin, 1,3-azaborin, 1,4-azaborin, borazine, and these. Aza analogs are preferred. Further, the heteroaryl group may be optionally substituted.

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

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

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

In some examples, preferred common substituents are deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile. , Isonitrile, sulfanyl, boron, and combinations thereof.

In some examples, more preferred common substituents consist of deuterium, fluorine, alkyl, cycloalkyl, alkoxy, aryloxy, amino, silyl, boryl, aryl, heteroaryl, sulfanyl, and combinations thereof. Selected from the group.

In yet another example, the most preferred common substituent is selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof.

The terms "substituted" and "substituent" refer to substituents other than H that are attached to relevant positions (eg, carbon or nitrogen). For example, if R ¹ represents a mono-permutation, then one R ¹ must be something other than H (ie, permutation). Similarly, if R ¹ represents a permutation, then the two of R ¹ must be other than H. Similarly, if R ¹ represents zero or unsubstituted, then R ¹ can be hydrogen at the available valence of the ring atom, as in the case of the carbon atom in benzene and the nitrogen atom in pyrrol, for example. In the case of a ring atom with a possible or fully filled valence (eg, nitrogen in pyridine), it simply represents nothing. The maximum number of substitutions possible in a ring structure depends on the total number of valences available in the ring atom.

As used herein, "combinations of these" apply to form known or chemically stable configurations that can be conceived by those of skill in the art from the applicable list. Indicates that one or more members of the list will be combined. For example, alkyls and dehydrogens can be combined to form partially or fully dehydrogenated alkyl groups; halogens and alkyls can be combined to form alkyl halide substituents. Yes; halogens, alkyls, and aryls can be combined to form arylalkyl halides. In one example, the term substitution comprises 2-4 combinations of the listed groups. In another example, the term substitution comprises a combination of 2-3 groups. In yet another example, the term substitution comprises a combination of two groups. Preferred combinations of substituents include up to 50 atoms that are not hydrogen or deuterium, or up to 40 atoms that are not hydrogen or deuterium, or up to 30 atoms that are not hydrogen or deuterium. It includes. In many examples, the preferred combination of substituents comprises up to 20 atoms that are not hydrogen or deuterium.

The name "aza" in fragments described herein, such as aza-dibenzofuran, aza-dibenzothiophene, etc., means that one or more of the CH groups in each aromatic ring are replaced by nitrogen atoms. For example, but not limited to, azatriphenylene includes both dibenzo [f, h] quinoxaline and dibenzo [f, h] quinoline. One of ordinary skill in the art can easily imagine other nitrogen analogs of the above-mentioned aza derivatives, and it is intended that all such analogs are included by the terms described herein.

As used herein, "deuterium" refers to an isotope of hydrogen. The deuterated compound can be easily prepared using a method known in the art. For example, US Pat. No. 8,557,400, WO 2006/095951, and US Patent Application Publication No. 2011/0037057, which are incorporated by reference in their entirety, are replaced by deuterium. The preparation of the organometallic complex has been described. Further references are incorporated by reference in their entirety, Tetrahedron 2015, 71, 1425-30 (Ming Yan et al.) And Angew. Chem. Int. Ed. (Reviews) 2007, 46, 7744-65 (Atzrodt et al.), Deuterium of methylene hydrogen in benzylamine and efficient pathways for substituting aromatic ring hydrogen with deuterium are described, respectively. ..

When a molecular fragment is described as a substituent or attached to another moiety, its name is the fragment (eg, phenyl, phenylene, naphthyl, dibenzofuryl) or the entire molecule (eg,). , Benzene, naphthalene, dibenzofuran) may be described as. In the present specification, even if the representation of substituents or binding fragments is different, they are considered to be equivalent.

In some examples, a pair of adjacent substituents can optionally be bonded or fused to form a ring. Preferred rings are 5-membered, 6-membered, or 7-membered carbocycles or heterocycles, formed by examples of saturated ring moieties and paired substituents. Includes both examples where the portion of the ring is unsaturated. As used herein, "adjacent" means that two related substituents can be adjacent to each other and on the same ring, as long as a stable fused ring system can be formed, or biphenyl. It means that it can be on a ring of two neighbors with the two closest available replaceable positions, such as the 2nd and 2'positions in, and the 1st and 8th positions in naphthalene.
B. Compounds of the present disclosure

In one aspect, the present disclosure provides a compound comprising a first ligand L _A of formula 1.
Wherein each ^X 1 ^{to X 10} is C or N; maximum number of the N of ^X 1 ^{to X 10} in the same ring is an 3; ^{R A} and ^{R B,} respectively, from mono It represents the maximum acceptable substituted or unsubstituted a represents; L _a is complexed with the metal M; each R ^a and R ^B are independently hydrogen, or as defined herein a substituent selected from the group consisting of general substituents that; M may be coordinated with other ligands; the ligand L _a is combined with other ligands It can include tridentate, tetradentate, pentadentate, or hexadentate ligands; any two substituents can bond or condense with each other to form a ring.

In some embodiments of compounds, each R ^A and R ^B are independently hydrogen, or a substituent selected from the group consisting of the preferred common substituents as defined herein is there.

In some embodiments, M is selected from the group consisting of Ru, Os, Ir, Pd, Pt, Cu, Ag, and Au. In some embodiments, M is Pt. In embodiments M is Pt, the first ligand L _A, in combination with one or two other ligands, it is possible to form a tridentate or tetradentate ligand.

In some embodiments, at least one of R ^A and R ^B are 5-membered or 6-membered heterocyclic ring. In some embodiments, at least one of R ^A and R ^B are pyridine, pyrimidine, triazine, imidazole, pyrazole, are selected from the group consisting of triazole, and N- heterocyclic carbene.

In some embodiments, at least one of X ^{1 to} X ¹⁰ is N. In some embodiments, X ³ is N. In some embodiments, X ³ is N and the rest of X ^{1 to} X ¹⁰ is C. In some embodiments, each X ^{1 to} X ¹⁰ is C. In some embodiments, the two ^RA substituents combine with each other to form a 6-membered carbocycle or heterocycle. In some embodiments, two or more bonded R ^B substituents together, one or more, for 6-membered carbocyclic ring, or form a heterocyclic ring.

In some embodiments of the compound, the compound is a compound of formula 2 below.
Wherein, M is an Pd or Pt; ring C and ring D are each independently a 5-membered or 6-membered carbocyclic or heterocyclic ring; Z ¹ and Z ^2, each independently, C or N; W ¹ and W ² are C or N, respectively; ^RC and ^RD , respectively, represent the maximum permissible substitution from the thing, or no substitution. Represents; L ¹ , L ² , and L ³ are independently 1-atom or 2-atom linkers, or are direct bonds; m, n, and p are independently 0 or 1 respectively. And m + n + p = 2 or 3; each ^RC and R ^D is independently hydrogen, or is a substituent selected from the group consisting of common substituents as defined herein. Yes; any two substituents can bond or condense with each other to form a ring. In some embodiments, each ^RC and R ^D is a substituent independently selected from the group consisting of hydrogen or the common substituents defined herein. In some embodiments, p = 0 and L ¹ and L ² are independently selected from the group consisting of direct binding, O, S, CRR', SiRR', BR, and NR; Each R and R'is a substituent independently selected from the group consisting of hydrogen or the common substituents defined herein. In some embodiments, each R and R'is a substituent independently selected from the group consisting of hydrogen or preferred common substituents as defined herein.

In some embodiments of the compound, the compound is selected from the group consisting of:
In the formula, A ^{1 to} A ¹⁰ are independently C or N, and the maximum number of N atoms in the same ring is 3; X ^{11 to} X ¹⁴ are X ^{1 to} X ¹⁰ and have the same definition; ^{R E} and ^{R F} is, it has the same definition as ^{R C} and ^{R D; L 4} represents a linker; ^{R X} and ^{R Y} are each independently alkyl, cycloalkyl Selected from the group consisting of alkyl, heteroalkyl, heterocycloalkyl, aryl, heteroaryl, and combinations thereof; any two substituents can bond or condense with each other to form a ring.

In some embodiments of the compound, the compound is selected from the group consisting of:
In the formula, i is an integer of ^{1 to} 2000, and for each i, R ¹ , R ² , R ³ , R ⁴ , Y ¹ , and Y ² in formulas I to LVIII are defined as follows. ..
^Here, R ^{A1 to R A53} has the following structure:
R ^{B1 to} R ^B46 have the following structure:
R ^C1 ~R ^C292 has the following structure:

In some embodiments of the compound, the compound is selected from the group consisting of:
C. OLEDs and devices of the present disclosure

In another aspect, the disclosure also provides an OLED device comprising a first organic layer containing the compounds disclosed in said compounds section of the present disclosure.

In some embodiments, the OLED comprises an anode, a cathode, and an organic layer disposed between the anode and the cathode. The organic layer may comprise a compound comprising a first ligand L _A of formula 1.
Wherein each ^X 1 ^{to X 10} is C or N; maximum number of the N of ^X 1 ^{to X 10} in the same ring is an 3; ^{R A} and ^{R B,} respectively, from mono It represents the maximum acceptable substituents, or represents unsubstituted; L _a is complexed with the metal M; each R ^a and R ^B are independently hydrogen, or 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 a substituent selected from the group consisting of; M may be coordinated with other ligands; the ligand L _a is , Can be attached to other ligands to include tridentate, tetradentate, pentadentate, or hexadentate ligands; any two substituents can be attached or fused to each other to form a ring. Can be done.

In some embodiments, the organic layer can be a light emitting layer and the compounds described herein can be light emitting or non-light emitting dopants.

In some embodiments, the organic layer can further comprise a host, the host comprising benzo-condensed thiophene or triphenylene containing a benzo-condensed furan, and any substituent in the host is independent. Then, C _n H _{2n + 1} , OC _n H _{2n + 1} , OAr ₁ , N (C _n H _{2n + 1} ) ₂ , N (Ar ₁ ) (Ar ₂ ), CH = CH-C _n H _{2n + 1} , C ≡ C-C _n It can be a non-condensation substituent selected from the group consisting of H _{2n + 1} , Ar ₁ , Ar _1- Ar ₂ , C _n H _2n- Ar ₁ , or can be unsubstituted, where n is 1-10. Ar ₁ and Ar ₂ can be independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and their heteroaromatic analogs.

In some embodiments, the organic layer can further comprise a host, which is triphenylene, carbazole, indolocarbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, 5,9-dioxa-13b. -Boranaphtho [3,2,1-de] anthracene, aza-triphenylene, aza-carbazole, aza-indrocarbazole, aza-dibenzothiophene, aza-dibenzofuran, aza-dibenzoselenophene, and aza- (5,9-) It contains at least one chemical group selected from the group consisting of dioxa-13b-boronaft [3,2,1-de] anthracene).

In some embodiments, the host can be selected from a group of hosts selected from the group consisting of:

In some embodiments, the organic layer can further comprise a host, said host comprising a metal complex.

In some embodiments, the compounds described herein can be sensitizers, the device can further include an acceptor, said acceptor being a fluorescent emitter, a delayed fluorescent emitter. , And a combination thereof.

In yet another embodiment, the OLEDs of the present disclosure may also include a light emitting region containing the compounds disclosed in said compounds section of the present disclosure.

In some embodiments, the light emitting region may comprise a compound comprising a first ligand L _A of formula 1.
Wherein each ^X 1 ^{to X 10} is C or N; maximum number of the N of ^X 1 ^{to X 10} in the same ring is an 3; ^{R A} and ^{R B,} respectively, from mono It represents the maximum acceptable substituted or unsubstituted a represents; L _a is complexed with the metal M; each R ^a and R ^B are independently hydrogen, or as defined herein a substituent selected from the group consisting of general substituents that; M may be coordinated with other ligands; the ligand L _a is combined with other ligands It can include tridentate, tetradentate, pentadentate, or hexadentate ligands; any two substituents can bond or condense with each other to form a ring.

In yet another aspect, the present disclosure is also 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 is: Provided are consumer products comprising an OLED containing the compounds disclosed in the compounds section of the present disclosure.

In some embodiments, the consumer product is an OLED having an anode, a cathode, and an organic layer disposed between the anode and the cathode, wherein the organic layer is of formula 1 below. including an OLED may comprise a compound comprising a first ligand _{L a.}
Wherein each ^X 1 ^{to X 10} is C or N; maximum number of the N of ^X 1 ^{to X 10} in the same ring is an 3; ^{R A} and ^{R B,} respectively, from mono It represents the maximum acceptable substituted or unsubstituted a represents; L _a is complexed with the metal M; each R ^a and R ^B are independently hydrogen, or as defined herein a substituent selected from the group consisting of general substituents that; M may be coordinated with other ligands; the ligand L _a is combined with other ligands It can include tridentate, tetradentate, pentadentate, or hexadentate ligands; any two substituents can bond or condense with each other to form a ring.

In some embodiments, the consumer product is a flat panel display, computer monitor, medical monitor, television, bulletin board, indoor or outdoor lighting and / or signal transmission light, head-up display, fully or partially transparent display, Flexible displays, laser printers, phones, mobile phones, tablets, fablets, personal digital assistants (PDAs), wearable devices, laptop computers, digital cameras, camcoders, viewfinders, diagonal microdisplays less than 2 inches, 3- It can be one of a D-display, a virtual reality or augmented reality display, a vehicle, a video wall including multiple displays side by side, a theater or stadium screen, a phototherapy device, and a sign.

In general, an OLED comprises at least one organic layer located between the anode and the cathode and electrically connected to them. When an electric current is applied, the anode injects holes and the cathode injects electrons into the organic layer (s). The injected holes and electrons move to the back-charged electrodes, respectively. When electrons and holes are localized on the same molecule, "excitons", which are localized electron-hole pairs with an excited energy state, are formed. Light is emitted via a photoelectron emission mechanism when excitons are relaxed. In some cases, excitons can be localized on excimers or excimers. Non-radiation mechanisms such as thermal relaxation may occur, but are generally considered undesirable.

US Pat. No. 5,844,363, US Pat. No. 6,303,238, and US Pat. No. 5,707,745, in which some OLED materials and configurations are incorporated by reference in their entirety. It is described in the specification.

Early OLEDs use luminescent molecules (“fluorescence”) that emit light from their singlet state, for example, as disclosed in US Pat. No. 4,769,292, which is incorporated by reference in its entirety. Was. Fluorescence generally occurs in a time frame of less than 10 nanoseconds.

Most recently, OLEDs with luminescent materials (“phosphorescent”) that emit light from the triplet state have been demonstrated. Baldo et al., "Highly Effective Phosphorescent Emissions from Organic Electroluminescent Devices," Nature, Vol. 395, 151-154, 1998; ("Balde-ji" and organic light emtiting devices based on electroluminescence ”, Apple. Phys. Lett. , 75, No. 3, 4-6 (1999) ("Baldo-II"). Phosphorescence is described in more detail in US Pat. No. 7,279,704, paragraphs 5-6, incorporated by reference.

FIG. 1 shows an organic light emitting device 100. The figure is not always at a constant scale. The device 100 includes a substrate 110, an anode 115, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, a light emitting layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, and a protective layer 155. , Cathode 160, and barrier layer 170 may be included. The cathode 160 is a composite cathode having a first conductive layer 162 and a second conductive layer 164. The device 100 can be made by depositing the described layers in sequence. The properties and functions of these various layers as well as material examples are described in more detail in US7,279,704, 6-10 steps incorporated by reference.

Further examples are available for each of these layers. For example, flexible and transparent substrate-anode combinations are disclosed in US Pat. No. 5,844,363, which is incorporated by reference in its entirety. Examples of p- doped hole transport layer is, for as disclosed in U.S. Patent Application Publication No. 2003/0230980 which is incorporated by reference in its entirety, 50: _{F 4} in m-MTDATA at a molar ratio of -It is doped with TCNQ. Examples of luminescent materials and host materials are disclosed in US Pat. No. 6,303,238 of Thomasson et al., Incorporated in their entirety by reference. An example of an n-doped electron transport layer is Li-doped BPhen in a 1: 1 molar ratio as disclosed in US Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Is. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entirety, are metals such as Mg: Ag having a transparent, conductive, sputter-deposited ITO layer overlying. Disclosed are examples of cathodes that include composite cathodes with a thin layer of. The theory and use of blocking layers is described in more detail in US Pat. No. 6,097,147 and US Patent Application Publication No. 2003/0230980, which are incorporated by reference in their entirety. An example of an injection layer is provided in US Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of the protective layer can be found in US 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, a light emitting layer 220, a hole transport layer 225, and an anode 230. The device 200 can be made by depositing the described layers in sequence. The device 200 is referred to as an "inverted" OLED because the most common OLED configuration has a cathode located above the anode and the device 200 has a cathode 215 located below the anode 230. Can be done. Materials similar to those described for device 100 may be used in the corresponding layers of device 200. FIG. 2 provides an example of how some layers can be omitted from the structure of device 100.

The simple layered structures illustrated in FIGS. 1 and 2 are provided as non-limiting examples, and embodiments of the present disclosure may be used in connection with a wide variety of other structures. Understood. The particular materials and structures described are exemplary in nature and other materials and structures may be used. A functional OLED can be realized by combining the various layers described in various ways, or the layers can be omitted altogether 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. Many of the examples provided herein describe the various layers as containing a single material, but use a combination of materials, such as a mixture of hosts and dopants, or more generally a mixture. It is understood that you can do it. Moreover, the layer may have various sub-layers. The names given to the various layers herein are not intended to be strictly limited. For example, in device 200, the hole transport layer 225 transports holes and injects holes into the light emitting layer 220, which can be described as a hole transport layer or a hole injection layer. In one embodiment, the OLED can be described as having an "organic layer" located between the cathode and the anode. The organic layer may include a single layer, or may further include multiple layers of different organic materials as described, for example, with respect to FIGS. 1 and 2.

Structures and materials not specifically described, such as OLEDs composed of polymeric materials, such as those disclosed in US Pat. No. 5,247,190 of Friend et al., Incorporated in their entirety by reference. May be used. As a further example, OLEDs with a single organic layer can be used. OLEDs may be stacked, for example, as described in US Pat. No. 5,707,745 of Forest et al., Incorporated in its entirety by reference. The OLED structure may deviate from the simple layered structure illustrated in FIGS. 1 and 2. For example, the substrate is described in US Pat. No. 6,091,195 of Forest et al., Which is incorporated by reference in its entirety, and / or in US Pat. No. 5,834,893 of Bruvic et al. It may include an angled reflective surface to improve out-coupling, such as a recessed structure.

Unless otherwise specified, any of the layers of the various embodiments can be deposited by any suitable method. For organic layers, preferred methods are those described in US Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entirety, by thermal deposition, inkjet, reference in whole. Described in Organic Vapor Deposition (OVPD), such as those described in US Pat. No. 6,337,102 of Forest et al., Which incorporates, and in US Pat. No. 7,431,968, which is incorporated in its entirety by reference. Includes deposition by organic vapor phase jet printing (OVJP), such as those that have been. Other suitable deposition methods include spin coating and other solution-based processes. The solution-based process is preferably carried out in nitrogen or an inert atmosphere. For other layers, preferred methods include thermal deposition. Preferred patterning methods are masks such as those described in US Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entirety, deposition via cold pressure welding, and inkjet. And patterning related to some of the deposition methods such as organic vapor jet printing (OVJP). Other methods may be used. The material to be deposited can be modified to be compatible with the particular deposition method. For example, substituents such as alkyl and aryl groups that are branched or non-branched and preferably contain at least 3 carbons are used in small molecules to enhance their ability to undergo solution processing. Can be done. Substituents having 20 or more carbons may be used, with 3 to 20 carbons being the preferred range. Materials with an asymmetric structure may have better solution processability than those with a symmetric structure, as asymmetric materials may be less prone to recrystallization. Dendrimer substituents can be used to enhance the ability of small molecules to undergo solution processing.

Devices made according to embodiments of the present disclosure may further include a barrier layer. One purpose of the barrier layer is to protect the electrodes and organic layer from damaging exposure to harmful species in the environment, including moisture, vapor and / or gas. The barrier layer can be deposited on, below or next to the substrate, electrodes, or on any other part of the device, including the edges. The barrier layer may include a single layer or multiple layers. The barrier layer can be formed by various known chemical vapor deposition techniques and may include a composition having a single phase and a composition having a polyphase. Any suitable material or combination of materials may be used for the barrier layer. The barrier layer may incorporate inorganic and / or organic compounds. Preferred barrier layers are described in US Pat. No. 7,968,146, PCT Patent Application Nos. PCT / US2007 / 023098 and PCT / US2009 / 042829, which are incorporated herein by reference in their entirety. Includes a mixture of polymeric and non-polymeric materials. To be considered a "mixture", the polymeric and non-polymeric materials, including the barrier layer, should be deposited under the same reaction conditions and / or simultaneously. The weight ratio of the polymeric material to the non-polymeric material can be in the range of 95: 5 to 5:95. Polymeric and non-polymeric materials can be made from the same precursor material. In one example, a mixture of polymeric and non-polymeric materials consists essentially of polymeric and inorganic silicon.

Devices made according to embodiments of the present disclosure can be incorporated into a wide variety of electronic component modules (or units) that can be incorporated into various electrical products or intermediate components. Such electrical products or intermediate components include display screens, lighting devices (discrete light source devices, lighting panels, etc.) that can be used by end-user product manufacturers. Such electronic component modules can optionally include drive electronics and / or power supplies. Devices made according to embodiments of the present disclosure can be incorporated into a wide variety of consumer products having one or more electronic component modules (or units) incorporated. A consumer product comprising an OLED containing the compounds of the present disclosure in the organic layer of the OLED is disclosed. Such consumer products include any type of product, including one or more light sources and / or one or more visual displays of some kind. Some examples of such consumer products include flat panel displays, curved displays, computer monitors, medical monitors, televisions, bulletin boards, indoor or outdoor lighting and / or signal transmission lights, head-up displays, complete. Or partially transparent display, flexible display, rollable display, foldable display, stretchable display, laser printer, phone, mobile phone, tablet, fablet, personal digital assistant (PDA), wearable device, wrap Top computers, digital cameras, camcoders, viewfinders, microdisplays (diagonal displays less than 2 inches), 3-D displays, virtual reality or augmented reality displays, vehicles, video walls including multiple displays side by side, theaters or Includes stadium screens, phototherapy devices, and signs. Various control mechanisms, including passive and active matrices, can be used to control devices manufactured in accordance with the present disclosure. Many devices are intended for use within a temperature range that is comfortable for humans, such as 18 to 30 degrees Celsius, more preferably room temperature (20-25 degrees Celsius), but outside this temperature range, for example, degrees Celsius. It can also be used at −40 ° C. to + 80 ° C.

Further details regarding OLEDs, and the definitions described above, can be found in US Pat. No. 7,279,704, which is incorporated 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 use the materials and structures. More generally, organic devices such as organic transistors can use the materials and structures.

In some embodiments, the OLED has one or more properties selected from the group consisting of being flexible, being rollable, being foldable, being able to be stretched, and being able to be bent. Has. In some embodiments, the OLED is transparent or translucent. In some embodiments, the OLED further comprises a layer containing carbon nanotubes.

In some embodiments, the OLED further comprises a layer comprising a delayed fluorescence emitter. In some embodiments, the OLED comprises an RGB pixel array or a white and color filter pixel array. In some embodiments, the OLED is a mobile device, handheld device, or wearable device. In some embodiments, the OLED is a display panel with a diagonal of less than 10 inches or an area of less than 50 square inches. In some embodiments, the OLED is a display panel having an area of at least 10 inches diagonal or at least 50 square inches. In some embodiments, the OLED is a lighting panel.

In some embodiments, the compound can be a luminescent dopant. In some embodiments, the compound is phosphorescent, fluorescent, thermally activated delayed fluorescence, or TADF (also referred to as E-type delayed fluorescence; eg, US Application 15/700,352, which is incorporated by reference in its entirety. Emissions can be generated through triplet-triplet annihilation, or a combination of these processes. In some embodiments, the luminescent dopant can be a racemic mixture or can be enriched with one enantiomer. In some embodiments, the compound can be homoreptic (each ligand is the same). In some embodiments, the compound can be heteroreptic (at least one ligand is different from the others). If there is more than one ligand coordinating to the metal, in some embodiments these ligands can all be the same. In some other embodiments, at least one ligand is different from the other ligand. In some embodiments, all ligands can be different from each other. This means that the ligand coordinated to the metal binds to other ligands coordinated to the metal to form a tridentate, tetradentate, pentadentate, or hexadental ligand. This also applies to embodiments where it is possible. Thus, if the coordinating ligands are bound to each other, in some embodiments all of the ligands can be identical and in some other embodiments they are bound. At least one of the ligands can be different from the other ligands.

In some embodiments, the compound can be used as a phosphorescent sensitizer in an OLED, where one or more layers in the OLED are one or more fluorescent and / or delayed fluorescent emitters. Includes acceptors in the form of. In some embodiments, the compound can be used as one component of excimer used as a sensitizer. As a phosphorescent photosensitizer, the compound must be capable of energy transfer to the acceptor, which either emits energy or further transfers energy to the final illuminant. The acceptor concentration can be in the range of 0.001% to 100%. The acceptor may be in the same layer as the phosphorescent sensitizer, or it may be 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 luminescence can result from any or all of the sensitizer, the acceptor, and the final illuminant.

According to another aspect, compositions comprising the compounds described herein are also disclosed.

The OLEDs disclosed herein can be incorporated into one or more consumer products, electronic component modules, and lighting panels. The organic layer can be a light emitting layer, in some embodiments the compound can be a light emitting dopant, and in other embodiments the compound is a non-light emitting dopant. Can be done.

In yet another aspect of the present disclosure, compositions comprising the novel compounds disclosed herein are described. The composition is one or more selected from the group consisting of solvents, hosts, hole injecting materials, hole transporting materials, electron blocking materials, hole blocking materials, and electron transporting materials disclosed herein. It can also contain ingredients.

The present disclosure includes any chemical structure, including novel compounds of the present disclosure, or monovalent or polyvalent variants thereof. In other words, the compounds of the invention or monovalent or polyvalent variants thereof can be part of a larger chemical structure. Such chemical structures can be selected from the group consisting of monomers, polymers, macromolecules, and supramolecular (also known as supramolecular). As used herein, a "monovalent variant of a compound" is identical to the compound, except that one hydrogen has been removed and replaced with a bond to the rest of the chemical structure. Refers to a certain part. As used herein, a "polyvalent variant of a compound" is identical to the compound except that more than one hydrogen has been removed and replaced with a bond to the rest of the chemical structure. Refers to a certain part. In the supramolecular example, the compound of invention can also be incorporated into the supramolecular complex without covalent bonds.
D. Combinations 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 can be used in combination with a wide variety of other materials present in the device. For example, the luminescent dopants disclosed herein can 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 referenced below are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and those skilled in the art may use other materials that may be useful in combination. Documents for identification can be easily browsed.
a) Conductive (conductive) dopant:

The charge transport layer is doped with a conductive dopant, which significantly changes the density of charge carriers, thereby changing their conductivity. Conductivity is increased by creating charge carriers in the matrix material or depending on the type of dopant, and changes in the Fermi level of the semiconductor can also be achieved. The hole transport layer can be doped with a p-type conductive dopant, and the n-type conductive dopant is used in the electron transport layer.

Non-limiting examples of conductive dopants that can be used in OLEDs in combination with the materials disclosed herein are exemplified below with the literature disclosing these materials.
EP01617493, EP01968131, EP2020694, EP2684932, US200050139810, US2007016905, US20090167167, US201208362, WO060881780, WO2009003455, WO2000900827, WO200901327, WO2014409310, US2007252140, US 20150120184
b) HIL / HTL:

The hole injection / transport material 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 injection / transport material. Examples of materials are phthalocyanine or porphyrin derivatives; aromatic amine derivatives; indolocarbazole derivatives; polymers containing fluorinated hydrocarbons; polymers with conductive dopants; conductive polymers such as PEDOT / PSS; phosphonic acids and silane derivatives. p-type semiconductor organic compound 1,4,5,8,9,12- hexaazatriphenylene hexa carbonitrile like; metal oxides derivatives such as MoO _x; self-assembling monomers derived from compounds such metal complexes, as well as cross-linking Including, but not limited to, sex compounds.

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

Each of Ar ¹ to Ar ⁹ is a group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene and azulene; dibenzothiophene. , Dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophen, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazol, oxatriazole, Dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiadin, indol, benzimidazole, indazole, indoxazine, benzoxazole, benzisooxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxalin A group consisting of aromatic heterocyclic compounds such as naphthylidine, phthalazine, pteridine, xanthene, aclysine, phenazine, phenothiazine, phenoxazine, benzoflopyridine, flodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine and selenophenodipyridine; The same or different types of groups selected from aromatic hydrocarbon cyclic groups and aromatic heterocyclic groups, and directly or directly or oxygen atoms, nitrogen atoms, sulfur atoms, silicon atoms, phosphorus atoms, It is selected from the group consisting of 2 to 10 cyclic structural units bonded to each other via at least one of a boron atom, a chain structural unit and an aliphatic cyclic group. Each Ar can be unsubstituted or dehydrogen, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, It can be substituted with a substituent selected from the group consisting of alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino and combinations thereof.

In one embodiment, Ar ¹ to Ar ⁹ are
(In the equation, k is an integer from 1 to 20; X ¹⁰¹ to X ¹⁰⁸ are C (including CH) or N; Z ¹⁰¹ is NA ¹ , O, or S; Ar ¹ is the above. It is independently selected from the group consisting of (has the same group as defined in).

Examples of metal complexes used in HIL or HTL include, but are not limited to, the following general formulas.
In the formula, Met is a metal that can have an atomic weight greater than 40; (Y ^101- Y ¹⁰² ) is a bidentate ligand, and Y ¹⁰¹ and Y ¹⁰² are C, N, O, P and S. L ¹⁰¹ is the co-ligand; k'is an integer value from 1 to the maximum number of ligands that can bind to the metal; and k'+ k''is the metal. The maximum number of ligands that can bind to.

In one embodiment, (Y ^101- Y ¹⁰² ) is a 2-phenylpyridine derivative. In another embodiment, (Y ^101- Y ¹⁰² ) is a carbene ligand. In another embodiment, the Met is selected from Ir, Pt, Os and Zn. In a further embodiment, the metal complex has a minimum oxidation potential of less than about 0.6 V in solution for the Fc ⁺ / Fc couple.

Non-limiting examples of HIL and HTL materials that can be used in OLEDs in combination with the materials disclosed herein are exemplified below with the literature disclosing these 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, US06517957, 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, US5061569, US5639914, WO05075451, WO07125714, WO08023550, WO08023759, WO2009145016, WO2010061824, WO2011075644, WO2012177006, WO2013018530, WO2013039073, WO2013087142, WO2013118812, WO2013120577, WO2013157367, WO2013175747, WO2014002873, WO2014015935, WO2014015937, WO2014030872, WO2014030921, WO2014403791, WO20141045414, WO2014157018
c) EBL:

The electron blocking layer (EBL) can be used to reduce the number of electrons and / or excitons emitted from the light emitting layer. The presence of such a blocking layer in the device can result in significantly higher efficiency and / or longer life compared to similar devices lacking the blocking layer. The blocking layer can also be used to limit light emission to the desired area of the OLED. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and / or higher triplet energy than the illuminant closest to the EBL interface. In some embodiments, the EBL material has a higher LUMO (closer to vacuum level) and / or higher triplet energy than one or more of the hosts closest to the EBL interface. In one embodiment, the compound used in EBL comprises the same molecule or the same functional group used as one of the hosts described below.
d) Host:

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

Examples of metal complexes used as host materials preferably have the following general formula:
In the formula, Met is a metal; (Y ^103- Y ¹⁰⁴ ) is a bidentate ligand, and Y ¹⁰³ and Y ¹⁰⁴ are independently selected from C, N, O, P and S; L ¹⁰¹ is Other ligands; k'is an integer value from 1 to the maximum number of ligands that can bind to the metal; and k'+ k''is the ligand that can bind to the metal. The maximum number.

In one aspect, the metal complex is the following complex.
In the formula, (ON) is a bidentate ligand having a metal coordinated to atoms O and N.

In another embodiment, the Met is selected from Ir and Pt. In a further embodiment, (Y ^103- Y ¹⁰⁴ ) is a carbene ligand.

In one embodiment, the host compound is an aromatic hydrocarbon cyclic compound such as benzene, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrycene, perylene, and azulene. Group consisting of: dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrologicpyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxa Diazol, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indol, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, Aromatic heterocyclic formulas such as cinnoline, quinazoline, quinoxalin, naphthylidine, phthalazine, pteridine, xanthene, aclysine, phenazine, phenothiazine, phenoxazine, benzoflopyridine, flodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine and selenophenodipyridine. A group of compounds; and groups of the same or different types selected from aromatic hydrocarbon cyclic and aromatic heterocyclic groups, and directly or directly or of oxygen, nitrogen, sulfur atoms. At least one of the group selected from the group consisting of 2 to 10 cyclic structural units bonded to each other via at least one of a silicon atom, a phosphorus atom, a boron atom, a chain structural unit and an aliphatic cyclic group. Including one. Each option within each group can be unsubstituted or dehydrogen, 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, and a substituent selected from the group consisting of combinations thereof. Can be done.

In one embodiment, the host compound comprises at least one of the following groups in the molecule:
In the formula, R ¹⁰¹ is hydrogen, dehydrogen, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, Ar mentioned above, selected from the group consisting of heteroaryls, acyls, carboxylic acids, ethers, esters, nitriles, isonitriles, sulfanyls, sulfinyls, sulfonyls, phosphinos, and combinations thereof, if it is aryl or heteroaryl. Has a definition similar to that of. k is an integer from 0 to 20 or 1 to 20. X ^{101 to} X ¹⁰⁸ are independently selected from C (including CH) or N. Z ¹⁰¹ and Z ¹⁰² are independently selected from NR ¹⁰¹ , O, or S.

Non-limiting examples of host materials that can be used in OLEDs in combination with the materials disclosed herein are exemplified below along with the literature disclosing these 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, US7154114, WO2001039234, WO2004093207, WO2005014551, WO2005089025, WO2006072002, WO2006114966, WO2007063754, WO2008056746, WO2009003898, WO2009021126, WO2009063833, WO2009066778, WO2009066779, WO2009086028, WO2010056066, WO2010107244, WO2011081423, WO2011081431, WO2011086863, WO2012128298, WO2012133644, WO2012133649, WO2013204872, WO2013305275, WO2013018315, WO2013191404, WO2014142472, US20170263869, US201601633995, US9466803
e) Additional illuminants:

One or more additional luminescent dopants can be used with the compounds of the present disclosure. Examples of the additional illuminant dopant are not particularly limited, and any compound can be used as long as the compound is typically used as a luminescent material. Examples of suitable luminous materials include phosphorescence, fluorescence, thermal activated delayed fluorescence, ie TADF (also known as E-type delayed fluorescence), triplet-triplet annihilation, or a combination of these processes. Examples include, but are not limited to, compounds capable of producing luminescence.

Non-limiting examples of luminescent materials that can be used in OLEDs in combination with the materials disclosed herein are illustrated below, along with literature disclosing these materials.
CN103694277, CN1696137, EB01238981, EP01239526, EP01961743, EP1239526, EP1244155, EP1642951, EP1647554, EP1841834, EP1841834B, EP2062907, EP2730583, JP2012074444, JP2013110263, JP4478555, KR1020090133652, KR20120032054, KR20130043460, TW201332980, US06699599, US06916554, 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, US20111227049, US2011285275, U S2012292601, US20130146848, US2013033172, US2013165653, US2013181190, US2013334521, US20140246656, US2014103305, US6303238, US6413656, US6653654, US6670645, US6687266, US6835469, US6921915, US7279704, US7332232, US7378162, US7534505, US7675228, US7728137, US7740957, US7759489, US7951947, US8067099, US8592586, US8871361, 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, WO201408882, WO2014402337, WO2014024131, WO20144031977, WO2014038456, WO2014112450
f) HBL:

The hole blocking layer (HBL) can be used to reduce the number of holes and / or excitons emitted from the light emitting layer. The presence of such a blocking layer in the device can result in significantly higher efficiency and / or longer life compared to similar devices lacking the blocking layer. The blocking layer can also be used to limit light emission to the desired area of the OLED. In some embodiments, the HBL material has lower HOMO (further away from the vacuum level) and / or higher triplet energy than the illuminant closest to the HBL interface. In some embodiments, the HBL material has lower HOMO (further away from the vacuum level) and / or higher triplet energy than one or more of the hosts closest to the HBL interface.

In one aspect, the compound used in the HBL comprises the same molecule or the same functional group as used for the host described above.

In another embodiment, the compound used in the HBL comprises at least one of the following groups in the molecule.
In the formula, k is an integer from 1 to 20; L ¹⁰¹ is another ligand and k'is an integer from 1 to 3.
g) ETL:

The electron transport layer (ETL) may include materials capable of transporting electrons. The electron transport layer may be genuine (undoped) or doped. Doping can be used to enhance conductivity. Examples of ETL materials are not particularly limited and any metal complex or organic compound may be used as long as it is typically used to transport electrons.

In one embodiment, the compound used in the ETL contains at least one of the following groups in the molecule.
In the formula, R ¹⁰¹ is hydrogen, dehydrogen, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, Selected from the group consisting of heteroaryls, acyls, carboxylic acids, ethers, esters, nitriles, isonitriles, sulfanyls, sulfinyls, sulfonyls, phosphinos and combinations thereof, where if it is aryl or heteroaryl, of Ar mentioned above. It has the same definition as the one. Ar ¹ to Ar ³ have similar definitions to those of Ar mentioned above. k is an integer from 1 to 20. X ¹⁰¹ to X ¹⁰⁸ are selected from C (including CH) or N.

In another embodiment, the metal complex used in the ETL contains, but is not limited to, the following general formula:
In the formula, (ON) or (NN) is a bidentate ligand having a metal coordinated to the atom O, N or N, N; L ¹⁰¹ is another ligand. K'is an integer value from 1 to the maximum number of ligands that can bond to the metal.

Non-limiting examples of ETL materials that can be used in OLEDs in combination with the materials disclosed herein are exemplified below with the literature disclosing these 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, US666612, US8415031, WO20003060956, WO200711263, WO200194869, WO201007994, WO20100072300, WO2011574770, WO2011105733, WO2013079217, WO2013145667, WO20131804376, WO201410445499,
h) Charge generation layer (CGL)

In tandem or laminated OLEDs, CGL plays an important role in performance and consists of an n-doped layer and a p-doped layer for electron and hole injection, respectively. Electrons and holes are supplied from the CGL and electrodes. The consumed electrons and holes in the CGL are refilled with electrons and holes injected from the cathode and anode, respectively, after which the bipolar current gradually reaches a stable state. Typical CGL materials include n-type and p-type conductive dopants used in the transport layer.

In any of the compounds mentioned above used in each layer of the OLED device, the hydrogen atom may be partially or completely deuterated. Thus, any specifically listed substituents such as, but not limited to, methyl, phenyl, pyridyl, etc. are not deuterated, partially deuterated, and fully deuterated. It can be a hydrogenated version. Similarly, the classes of substituents such as, but not limited to, alkyl, aryl, cycloalkyl, heteroaryl, etc. are also non-deuterated, partially deuterated, and fully deuterated. Can be a hydrogenated version.

It is understood that the various embodiments described herein are merely examples and are not intended to limit the scope of the invention. For example, many of the materials and structures described herein can be replaced with other materials and structures without departing from the spirit of the invention. Accordingly, the invention as claimed can include variations from the particular examples and preferred embodiments described herein, as will be apparent to those skilled in the art. It is understood that the various theories as to why the present invention works are not intended to be limiting.

Material synthesis

Synthesis of 7-bromo-3,4-dihydronaphthalene-1-yl trifluoromethanesulfonate
7-Bromo-3,4-dihydronaphthalene-1 (2H) -one (45.0 g, 200 mmol) and 1,1,1-trifluoro-N-phenyl-N-((trifluoromethyl) sulfonyl) methanesulfone The amide (79.0 g, 220 mmol) was dissolved in dry THF (1000 ml). This was cooled to −78 ° C., and a 15% solution of potassium bis (trimethylsilyl) amide in toluene (314 ml, 220 mmol) was added. The reaction mixture was stirred at −78 ° C. for 3 hours. The reaction mixture was left overnight and warmed to room temperature under nitrogen. After all 7-bromo-3,4-dihydronaphthalene-1 (2H) -one was consumed, the reaction was quenched by the addition of water (50 ml). The crude product is then purified by flash chromatography in a standard silica solid phase with a mixture of heptane and dichloromethane and 7-bromo-3,4-dihydronaphthalene-1-yl trifluo as a pale yellow oil. Dichloromethane sulfonate (68.9 g, 193 mmol, 96% yield) was obtained.

Synthesis of 6-bromo-4- (3-chlorophenyl) -1,2-dihydronaphthalene
7-Bromo-3,4-dihydronaphthalene-1-yl trifluoromethanesulfonate (68.9 g, 193 mmol), (3-chlorophenyl) boronic acid (30.2 g, 193 mmol), and Cs ₂ CO ₃ (157 g, 482 mmol). ) Was dissolved in deoxygenated dioxane (1000 ml). [1,1'-Bis (diphenylphosphino) ferrocene] Dichloropalladium (II) (complex with dichloromethane) (7.86 g, 9.65 mmol) was added, and the reaction mixture was added under nitrogen overnight (~ 16 hours) Stirred at room temperature. (3-Chlorophenyl) Boronic acid (2.00 g, 12.8 mmol) and [1,1'-bis (diphenylphosphino) ferrocene] Dichloropalladium (II) (complex with dichloromethane) (3.00 g, 3.67 mmol) ) Was added, and the reaction mixture was stirred under nitrogen overnight at room temperature. The reaction mixture was then heated to 50 ° C. for 4 hours. The solvent is evaporated and the crude product is then purified by flash chromatography with heptane in a standard silica solid phase to as a colorless oil 6-bromo-4- (3-chlorophenyl) -1,2-. Dihydronaphthalene (53.9 g, 169 mmol, 87% yield) was obtained.

Synthesis of 7-bromo-1- (3-chlorophenyl) naphthalene
6-Bromo-4- (3-chlorophenyl) -1,2-dihydronaphthalene (53.9 g, 169 mmol) was dissolved in DCM (1000 ml). 2,3-Dichloro-5,6-dicyanobenzoquinone (DDQ) (57.4 g, 253 mmol) was added at room temperature and the reaction mixture was stirred under nitrogen overnight at 50 ° C. The reaction mixture was cooled to room temperature and NaHCO ₃ (saturated aqueous solution, 800 ml) and DCM (300 ml) were added. The organic layer was separated and the aqueous layer was washed with DCM (500 ml). The combined organic layers were dried over sulfonyl ₄ to evaporate the volatiles. The resulting crude brown oil was purified by flash chromatography with heptane in a standard silica solid phase to give 7-bromo-1- (3-chlorophenyl) naphthalene (41.0 g, 129 mmol) as a pale yellow oil. , 77% yield) was obtained.

4,4,5,5-Tetramethyl-2-(3-(7- (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) naphthalene-1-yl) phenyl) )-1,3,2-Synthesis of dioxaborolane
7-Bromo-1- (3-chlorophenyl) naphthalene (6.00 g, 18.9 mmol), bis (pinacolato) diboron (19.19 g, 75.6 mmol), potassium acetate (9.27 g, 94.5 mmol), and 500 mL 3-necked round bottom with dicyclohexyl (2', 6'-dimethoxy- [1,1'-biphenyl] -2-yl) phosphine (SPhos) (1.55 g, 3.78 mmol) connected to a reflux condenser It was dissolved in dry dioxane (120 mL) in a flask. The mixture was spurged with nitrogen for 15 minutes, then tris (dibenzylideneacetone) dipalladium (0) (1.73 g, 1.89 mmol) was added and additional degassing was performed for an additional 15 minutes. The reaction mixture was then stirred at 100 ° C. for 18 hours. After cooling to room temperature, the reaction mixture was filtered through a Celite cartridge to remove volatiles under vacuum. The resulting dark brown crude mixture was extracted with ethyl acetate (100 mL x 2) and washed with brine (100 mL). The combined organic phases were dried over magnesium sulfate and the solvent was removed under vacuum. The resulting crude mixture was purified by flash chromatography using a mixture of isohexane and ethyl acetate in a standard silica solid phase to give a pale yellow solid (4.18 g, 9.26 mmol, 49%).

Synthesis of 4- (tert-butyl) -2-(3- (7- (4- (tert-butyl) pyridin-2-yl) naphthalene-1-yl) phenyl) pyridine
4,4,5,5-Tetramethyl-2- [3- [7- (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) -1-naphthyl] phenyl] -1,3,2-dioxaborolane (3.50 g, 7.67 mmol), 4-tert-butyl-2-chloro-pyridine (5.21 g, 30.7 mmol), tripotassium phosphate (6.51 g, 30. 7 mmol) was dissolved in N, N-dimethylformamide (106 mL) in a 500 mL 3-necked round-bottom flask connected to a reflux condenser. The mixture was spurged with nitrogen for 15 minutes, then tetrakis (triphenylphosphine) palladium (0) (1.42 g, 1.23 mmol) was added and additional degassing was performed for an additional 15 minutes. The reaction mixture was then stirred at 100 ° C. for 18 hours. After cooling to room temperature, the reaction mixture was filtered through a Celite cartridge to remove volatiles under vacuum. The resulting dark brown crude mixture was extracted with ethyl acetate (100 mL x 2) and washed with brine (100 mL). The combined organic phases were dried over magnesium sulfate and the solvent was removed under vacuum. The resulting crude mixture was purified by flash chromatography using a mixture of isohexane and acetone in a standard silica solid phase and then milled with isohexane to a white solid (2.32 g, 4.91 mmol, 64%). Got

Synthesis of Example Compound I-A34 of the Present Invention
4- (tert-butyl) -2-(3-(7- (4- (tert-butyl) pyridin-2-yl) naphthalene-1-yl) phenyl) pyridine in 1,2-dichlorobenzene (10 mL) A mixture of (2.7 g, 5.74 mmol) and dichloro (1,5-cyclooctadiene) palladium (II) (2.15 g, 5.74 mmol) was spurged with nitrogen for 15 minutes. After refluxing for 6 days, the volatiles were removed under reduced pressure. The crude residue was purified by flash chromatography in a standard silica solid phase with a mixture of ethyl acetate and dichloromethane and then milled with methanol to a brown solid (0.25 g, 0.38 mmol, 6. 5%) was obtained.

Table 1 above shows the results of DFT calculations performed to determine the HOMO / LUMO level, HOMO-LUMO gap, and energy of the lowest triplet (T ₁ ) excited state of each compound. Data were collected using the program Gaussian 16. The geometry was optimized using the B3LYP function and the CEP-31G basis set system. Excited state energies were computerized by TDDFT with optimized ground state geometry. The THF solvent was simulated using a self-consistent reaction field to further improve the consistency with the experiment. Examples of the present invention The T ₁ energies of Compound I-A1, Compound I-A34, Compound I-A501, Compound II-A1, Compound XXXII-A1, and Compound XXXV-A1 are 713, 706, 732, 825, 718, And 710 nm. Both compounds exhibit phosphorescence in the deep red to near infrared (NIR) region due to the conjugated moiety of phenyl-naphthalene.

The photoluminescence (PL) spectrum of Example Compound I-A34 of the present invention obtained in a 2-methyl THF solution at room temperature is shown in FIG. The PL intensity was normalized for the first emission peak, which is the maximum. The maximum emission and the second emission peak of the compound I-A34 of the present invention are 658 nm and 723 nm. Due to the highly rigid and conjugated phenyl-naphthalene, the examples of the present invention exhibit deep red to near infrared emission. When the compound of the example of the present invention is used as a light emitting dopant for an organic electroluminescence device, it is expected to emit deep red to near infrared light with good device performance.

The calculations in the DFT function system and the basis function system described above are theoretical. Computerized composite protocols such as Gaussian09 with the B3LYP and CEP-31G protocols used herein have an additive electronic action, so that the larger basis set is a complete basis set (CBS). ) Relies on the assumption that it can be used for extrapolation to the limit. However, if the purpose of the study is to understand the variability of HOMO, LUMO, S ₁ , T ₁ , bond dissociation energy, etc. in a series of structurally related compounds, the additional effects are expected to be similar. .. Therefore, the absolute error due to the use of B3LYP can be significant compared to other computer methods, but between the values of HOMO, LUMO, S ₁ , T ₁ , and bond dissociation energy calculated by the B3LYP protocol. Relative differences are expected to reproduce the experiment very well. For example, Hong et al., Chem. Mater. See 2016, 28, 5791-98, 5792-93 and Supplemental Information (discussing the reliability of DFT calculations for OLED materials). Moreover, for iridium or platinum complexes useful in OLED technology, the data obtained by DFT calculations correlate very well with actual experimental data. Tavasli et al., J. Mol. Mater. Chem. 2012, 22, 6419-29, 6422 (Table 3) (DFT calculations show that various luminescent complexes are highly correlated with actual data); Morello, G. et al. R. , J. Mol. Model. See 2017, 23: 174 (studying various DFT and basis set systems and concluding that the combination of B3LYP and CEP-31G is particularly accurate for luminescent complexes).

100 Organic light emitting device 110 Substrate 115 Anode 120 Hole injection layer 125 Hole transport layer 130 Electron blocking layer 135 Light emitting layer 140 Hole blocking layer 145 Electron transport layer 150 Electron injection layer 155 Protective layer 160 Cathode 162 First conductive layer 164 Second Conductive Layer 170 Barrier Layer 200 Inverted OLED, Device 210 Substrate 215 Cone 220 Emitting Layer 225 Hole Transport Layer 230 Anode

Claims (16)

_A compound comprising the first ligand LA of the following formula 1.
(During the ceremony,
Each X ^{1 to} X ¹⁰ is C or N;
The maximum number of X ^{1 to} X ¹⁰ as N in the same ring is 3;
R ^A and R ^B, respectively, represents the maximum acceptable substituents from mono-, or an unsubstituted;
L _A is complexed with the metal M;
Each R ^A and R ^B are independently hydrogen, or 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 substituents selected from the group consisting of combinations thereof;
M can coordinate with other ligands;
The ligand L _A is combined with other ligands, tridentate, tetradentate, it can include a pentadentate, or hexadentate ligand;
Any two substituents can be bonded or condensed with each other to form a ring. ) The compound according to claim 1, wherein M is selected from the group consisting of Ru, Os, Ir, Pd, Pt, Cu, Ag, and Au. The first ligand L _A is bonded to one or two other ligands, compounds of claim 1 to form a tridentate or tetradentate ligand. At least one of R ^A and R ^B is The compound of claim 1 which is 5-membered or 6-membered heterocyclic ring. At least one of R ^A and R ^B, pyridine, pyrimidine, triazine, imidazole, pyrazole, triazole, and the compound of claim 1 selected from the group consisting of N- heterocyclic carbene. The compound according to claim 1, wherein at least one of X ^{1 to} X ¹⁰ is N, or each X ^{1 to} X ¹⁰ is C. The compound according to claim 1, wherein two ^RA substituents are bonded to each other to form a 6-membered carbon ring or a heterocycle. Two or more bonded R ^B substituents together, one or more, 6-membered carbocyclic ring, or a compound according to claim 1 to form a heterocyclic ring. The compound according to claim 1, which is a compound of the following formula 2.
(During the ceremony,
M is Pd or Pt;
Rings C and D are independently 5- or 6-membered carbon or heterocycles;
Z ¹ and Z ² are C or N, respectively;
W ¹ and W ² are C or N, respectively;
^RC and R ^D independently represent the maximum permutable substitution from the thing, or no substitution;
L ¹ , L ² , and L ³ are independently one-atom or two-atom linkers, or direct bonds;
m, n, and p are independently 0 or 1;
m + n + p = 2 or 3;
Each ^RC and R ^D is independently hydrogen, or deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, hetero. A substituent selected from the group consisting of aryl, nitrile, isonitrile, sulfanyl, boryl, and combinations thereof;
Any two substituents can be bonded or condensed with each other to form a ring. ) p = 0 and L ¹ and L ² are independently selected from the group consisting of direct binding, O, S, CRR', SiRR', BR, and NR;
Each R and R'is independently hydrogen, or dehydrogen, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl. , Nitrile, isonitrile, sulfanyl, boron, and the compound according to claim 9, which is selected from the group consisting of combinations thereof. The compound according to claim 1, which is selected from the group consisting of the following.
(During the ceremony,
A ^{1 to} A ¹⁰ are independently C or N, and the maximum number of N atoms in the same ring is 3;
X ^{11 to} X ¹⁴ have the same definition as X ^{1 to} X ¹⁰ ;
^RE and R ^F have the same definition as ^RC and R ^D ;
L ⁴ represents a linker;
^RX and ^RY are independently selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, aryl, heteroaryl, and combinations thereof;
Any two substituents can be bonded or condensed with each other to form a ring. ) The compound according to claim 1, which is selected from the group consisting of the following.
(In the formula, i is an integer from ^{1 to} 2000, and for each i, R ¹ , R ² , R ³ , R ⁴ , Y ¹ , and Y ² in formulas I to LVIII are defined as follows. )
^(Wherein, R ^{A1 to R A53} has the following structure.)
^(R B1 ^{to R B46} has the following structure.)
^(R C1 ~R ^C292 has the following structure.)
The compound according to claim 12, which is selected from the group consisting of the following.
With the anode
With the cathode
An organic light emitting device (OLED) including an organic layer arranged between the anode and the cathode.
The organic light emitting device wherein the organic layer, which comprises a compound containing a first ligand L _A of formula 1 (OLED).
(During the ceremony,
Each X ^{1 to} X ¹⁰ is C or N;
The maximum number of X ^{1 to} X ¹⁰ as N in the same ring is 3;
R ^A and R ^B, respectively, represents the maximum acceptable substituents from mono-, or an unsubstituted;
L _A is complexed with the metal M;
Each R ^A and R ^B are independently hydrogen, or 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 substituents selected from the group consisting of combinations thereof;
M can coordinate with other ligands;
The ligand L _A is combined with other ligands, tridentate, tetradentate, it can include a pentadentate, or hexadentate ligand;
Any two substituents can be bonded or condensed with each other to form a ring. ) A consumer product comprising the OLED according to claim 14. A composition comprising the compound according to claim 1.