Organic electroluminescent materials and devices

Abstract

Bis(tridentate) osmium(II) complexes containing phosphite groups useful as phosphorescent emitters are disclosed. The disclosed osmium(II) complexes have higher oxidation potential then previously known osmium(II) complexes. An organic light emitting device having an organic layer that includes the disclosed osmium(II) complex is also disclosed.

Claims

1. A compound having a structure selected from the group consisting of: ##STR00222## wherein ##STR00223## each independently represents a tridentate ligand coordinating to osmium through coordinating atoms of X, carbon and phosphorus; wherein X is selected from the group consisting of nitrogen, oxygen, sulfur, and carbon; and wherein (i) the compound is heteroleptic, (ii) the P of ##STR00224## is bonded to an O, (iii) the compound has a structure of Formula II, X is a neutral nitrogen atom of an imidazole ring, C is an anionic donor carbon, and P is a neutral donor phosphorus, or (iv) a combination of more than one of (i), (ii), and (iii).

2. The compound of claim 1, wherein X is a neutral nitrogen atom of an imidazole ring, C is an anionic donor carbon, and P is a neutral donor phosphorus.

3. The compound of claim 1, wherein the compound is neutral.

4. The compound of claim 1, wherein X is a carbon, and Os—X bond is a metal-carbene bond.

5. The compound of claim 1, wherein the compound is homoleptic.

6. The compound of claim 1, wherein the compound is heteroleptic.

7. The compound of claim 1, wherein the compound has the structure of ##STR00225##

8. The compound of claim 1, wherein the compound has the structure of ##STR00226## wherein each of R.sup.1 and R.sup.2 is phenol or phenyl; wherein Y is oxygen; wherein ring A comprises a heterocyclic ring comprising pyridine, imidazole, pyrazole, NHC carbene, or quninoline; wherein R.sup.3 is alkyl; wherein R.sup.3 can represent mono-, di-, or tri-substitutions, or no substitution; and wherein any two adjacent substituents of R.sup.1, R.sup.2, and R.sup.3 are optionally joined to form a ring.

9. The compound of claim 1, wherein the compound is selected from the group consisting of ##STR00227## ##STR00228## ##STR00229## ##STR00230## ##STR00231## ##STR00232## ##STR00233## ##STR00234##

10. A first device comprising a first organic light emitting device, the first organic light emitting device comprising: an anode; a cathode; and an organic layer, disposed between the anode and the cathode, comprising a compound having a structure selected from the group consisting of: ##STR00235## wherein ##STR00236## each independently represents a tridentate ligand coordinating to osmium through coordinating atoms of X, carbon and phosphorus; wherein X is selected from the group consisting of nitrogen, oxygen, sulfur, and carbon; and wherein (i) the compound is heteroleptic, (ii) the P of ##STR00237## is bonded to an O, (iii) the compound has a structure of Formula II, X is a neutral nitrogen atom of an imidazole ring, C is an anionic donor carbon, and P is a neutral donor phosphorus, or (iv) a combination of more than one of (i), (ii), and (iii).

11. The first device of claim 10, wherein X is a neutral nitrogen atom of an imidazole ring, C is an anionic donor carbon, and P is a neutral donor phosphorus.

12. The first device of claim 10, wherein the compound has the structure of ##STR00238## wherein R.sup.1 and R.sup.2 is phenol or phenyl; wherein Y is oxygen; wherein ring A comprises a heterocyclic ring comprising pyridine, imidazole, pyrazole, NHC carbene, or quninoline; wherein R.sup.3 is alkyl; wherein R.sup.3 can represent mono-, di-, or tri-substitutions, or no substitution; and wherein any two adjacent substituents of R.sup.1, R.sup.2, and R.sup.3 are optionally joined to form a ring.

13. The first device of claim 10, wherein the first device is selected from the group consisting of a consumer product, an organic light emitting device, and a light panel.

14. The first device of claim 10, wherein the organic layer is an emissive layer and the compound is an emissive dopant.

15. The first device of claim 10, wherein the organic layer is an emissive layer and the compound is a non-emissive dopant.

16. The first device of claim 10, wherein the organic layer further comprises a host material.

17. The first device of claim 16, wherein the host material comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan; wherein any substituent in the host material is an unfused substituent independently selected from the group consisting of C.sub.nH.sub.2n+1, OC.sub.nH.sub.2n+1, OAr.sub.1, N(C.sub.nH.sub.2n+1).sub.2, N(Ar.sub.1)(Ar.sub.2), CH═CH—C.sub.nH.sub.2n+1, C≡C—C.sub.nH.sub.2n+1, Ar.sub.1, Ar.sub.1-Ar.sub.2, and C.sub.nH.sub.2n-Ar.sub.1—; wherein n is from 1 to 10; and wherein Ar.sub.1 and Ar.sub.2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.

18. The first device of claim 16, wherein the host material comprises at least one chemical group selected from the group consisting of carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.

19. The first device of claim 16, wherein the host material is selected from the group consisting of: ##STR00239## ##STR00240## ##STR00241## and combinations thereof.

20. The first device of claim 16, wherein the host material comprises a metal complex.

21. A formulation comprising a compound having a structure selected from the group consisting of: ##STR00242## wherein ##STR00243## each independently represents a tridentate ligand coordinating to osmium through coordinating atoms of X, carbon and phosphorus; wherein X is selected from the group consisting of nitrogen, oxygen, sulfur, and carbon; and wherein (i) the compound is heteroleptic, (ii) the P of ##STR00244## is bonded to an O, (iii) the compound has a structure of Formula II, X is a neutral nitrogen atom of an imidazole ring, C is an anionic donor carbon, and P is a neutral donor phosphorus, or (iv) a combination of more than one of (i), (ii), and (iii).

22. The compound of claim 1, wherein the P of ##STR00245## is bonded to an O.

23. The compound of claim 1, wherein the P of ##STR00246## is part of a phosphite moiety.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows an organic light emitting device.

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

(3) FIG. 3 shows Formulas I and II as disclosed herein.

(4) FIG. 4 shows the molecular structure of the inventive Compound 1.

(5) FIG. 5 is a graph showing a correlation between calculated HOMO level and oxidation potential (measured by cyclic voltammetry).

DETAILED DESCRIPTION

(6) 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.

(7) 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.

(8) 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”), which 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.

(9) 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.

(10) 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 F.sub.4-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.

(11) 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.

(12) 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 invention 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.

(13) 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.

(14) 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 OVJD. 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 is 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.

(15) Devices fabricated in accordance with embodiments of the present invention 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.

(16) Devices fabricated in accordance with embodiments of the invention may be incorporated into a wide variety of consumer products, including flat panel displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads up displays, fully transparent displays, flexible displays, laser printers, telephones, cell phones, personal digital assistants (PDAs), laptop computers, digital cameras, camcorders, viewfinders, micro-displays, 3-D displays, vehicles, a large area wall, theater or stadium screen, or a sign. Various control mechanisms may be used to control devices fabricated in accordance with the present invention, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18 degrees C. to 30 degrees C., and more preferably at room temperature (20-25 degrees C.), but could be used outside this temperature range, for example, from −40 degree C. to +80 degree C.

(17) 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.

(18) The terms halo, halogen, alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, heterocyclic group, aryl, aromatic group, and heteroaryl are known to the art, and are defined in U.S. Pat. No. 7,279,704 at cols. 31-32, which are incorporated herein by reference.

(19) As used herein, “substituted” indicates that a substituent other than H is bonded to the relevant carbon. Thus, where R.sup.2 is monosubstituted, then one R.sup.2 must be other than H. Similarly, where R.sup.3 is disubstituted, then two of R.sup.3 must be other than H. Similarly, where R.sup.2 is unsubstituted R.sup.2 is hydrogen for all available positions.

(20) According to an embodiment, novel phosphorus containing bis(tridentate) osmium complexes are disclosed. The inventors have discovered that these novel compounds are useful as emitters in phosphorescent OLEDs.

(21) Osmium (II) complexes have been investigated for OLED applications. (See Eur. J. Inorg. Chem. 2006, 3319-3332). The octahedral ligand arrangement of the Os(II) complexes resembles that of Ir(III) complexes. Os(II) complexes generally exhibit low oxidation potential, i.e. shallow HOMO energy level, than IR(III) complexes. Generally, the low oxidation potential make OS(II) complexes not compatible with the mainstream matrix materials in OLED devices. The low oxidation potential also presents difficulty in tuning the phosphorescence to the blue color regime.

(22) In the present disclosure, however, the inventors disclose novel osmium(II) complexes in which the above-mentioned problems have been solved by utilizing the high electron withdrawing property of phosphite. By incorporating phosphite groups in the molecule, the inventors have produced osmium(II) complexes with much deeper oxidation potential.

(23) According to an embodiment, a compound is provided that comprises a structure selected from the group consisting of:

(24) ##STR00004##
wherein

(25) ##STR00005##
each independently represents a tridentate ligand coordinating to osmium through coordinating atoms of X, carbon and phosphorus; and wherein X is selected from the group consisting of nitrogen, oxygen, sulfur, and carbon.

(26) According to other embodiments of the compound, X is a neutral donor atom, C is an anionic donor carbon, and P is a neutral donor phosphorus. The compound can be neutral.

(27) In one embodiment, X is a carbon, and Os—X bond is a metal-carbene bond. In another embodiment, the compound is homoleptic. In another embodiment, the compound is heteroleptic.

(28) In another, the compound has the structure of

(29) ##STR00006##

(30) In another embodiment, the compound has the structure of

(31) ##STR00007##
wherein each of R.sup.1 and R.sup.2 is phenol or phenyl;
wherein Y comprises carbon or oxygen;
wherein ring A comprises a heterocyclic ring comprising pyridine, imidazole, pyrazole, NHC carbene, or quinoline;
wherein R.sup.3 is alkyl;
wherein R.sup.3 can represent mono-, di-, or tri-substitutions, or no substitution; and
wherein any two adjacent substituents of R.sup.1, R.sup.2, and R.sup.3 are optionally joined to form a ring.

(32) In another embodiment, the compound is selected from the group consisting of

(33) ##STR00008## ##STR00009## ##STR00010## ##STR00011## ##STR00012## ##STR00013## ##STR00014## ##STR00015##

(34) According to another aspect of the present disclosure, a first device comprising a first organic light emitting device is disclosed. The first organic light emitting device comprises an anode; a cathode; and an organic layer, disposed between the anode and the cathode, comprising a compound having a structure selected from the group consisting of:

(35) ##STR00016##
wherein

(36) ##STR00017##
each independently represents a tridentate ligand coordinating to osmium through coordinating atoms of X, carbon and phosphorus; and wherein X is selected from the group consisting of nitrogen, oxygen, sulfur, and carbon.

(37) In an embodiment of the first device, X is a neutral donor atom, C is an anionic donor carbon, and P is a neutral donor phosphorus. In another embodiment of the first device, the compound has the structure of

(38) ##STR00018##
wherein R.sup.1 and R.sup.2 is phenol or phenyl;
wherein Y comprises carbon or oxygen;
wherein ring A comprises a heterocyclic ring comprising pyridine, imidazole, pyrazole, NHC carbene, or quninoline;
wherein R.sup.3 is alkyl;
wherein R.sup.3 can represent mono-, di-, or tri-substitutions, or no substitution; and
wherein any two adjacent substituents of R.sup.1, R.sup.2, and R.sup.3 are optionally joined to form a ring.

(39) The first device can be a consumer product. The first device can be an organic light emitting device. The first device can comprise a light panel.

(40) In another embodiment of the first device, the organic layer is an emissive layer and the compound is an emissive dopant. In another embodiment, the compound is a non-emissive dopant in the emissive layer.

(41) In another embodiment of the first device, the organic layer further comprises a host material. The host material can comprise a triphenylene containing benzo-fused thiophene or benzo-fused furan; wherein any substituent in the host material is an unfused substituent independently selected from the group consisting of C.sub.nH.sub.2n+1, OC.sub.nH.sub.2n+1, OAr.sub.1, N(C.sub.nH.sub.2n+1).sub.2, N(Ar.sub.1)(Ar.sub.2), CH═CH—C.sub.nH.sub.2n+1, C≡C—C.sub.nH.sub.2n+1, Ar.sub.1, Ar.sub.1-Ar.sub.2, C.sub.nH.sub.2n—Ar.sub.1, or no substitution;

(42) wherein n is from 1 to 10; and

(43) wherein Ar.sub.1 and Ar.sub.2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.

(44) In another embodiment, the host material comprises at least one chemical group selected from the group consisting of carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.

(45) In another embodiment, the host material is selected from the group consisting of

(46) ##STR00019## ##STR00020## ##STR00021##
and combinations thereof.

(47) In yet another embodiment, the host material comprises a metal complex.

(48) According to another aspect of the present disclosure, a novel formulation is disclosed. The formulation comprises a compound having a structure selected from the group consisting of:

(49) ##STR00022##
wherein

(50) ##STR00023##
each independently represents a tridentate ligand coordinating to osmium through coordinating atoms of X, carbon and phosphorus; and wherein X is selected from the group consisting of nitrogen, oxygen, sulfur, and carbon.
Combination with Other Materials

(51) 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.

(52) HIL/HTL:

(53) A hole injecting/transporting material to be used in the present invention 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 not limit to: a phthalocyanine or porphryin 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.sub.x; a p-type semiconducting organic compound, such as 1,4,5,8,9,12-Hexaazatriphenylenehexacarbonitrile; a metal complex, and a cross-linkable compounds.

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

(55) ##STR00024##

(56) Each of Ar.sup.1 to Ar.sup.9 is selected from the group consisting aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, azulene; group consisting 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 group consisting 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. Wherein each Ar is further substituted by a substituent selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

(57) In one aspect, Ar.sup.1 to Ar.sup.9 is independently selected from the group consisting of:

(58) ##STR00025##
wherein k is an integer from 1 to 20; X.sup.101 to X.sup.108 is C (including CH) or N; Z.sup.101 is NAr.sup.1, O, or S; Ar.sup.1 has the same group defined above.

(59) Examples of metal complexes used in HIL or HTL include, but not limit to the following general formula:

(60) ##STR00026##
wherein Met is a metal, which can have an atomic weight greater than 40; (Y.sup.101-Y.sup.102) is a bidentate ligand, Y.sup.101 and Y.sup.102 are independently selected from C, N, O, P, and S; L.sup.101 is 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.

(61) In one aspect, (Y.sup.101-Y.sup.102) is a 2-phenylpyridine derivative. In another aspect, (Y.sup.101-Y.sup.102) 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.sup.+/Fc couple less than about 0.6 V.

(62) Host:

(63) The light emitting layer of the organic EL device of the present invention 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. While the Table below categorizes host materials as preferred for devices that emit various colors, any host material may be used with any dopant so long as the triplet criteria is satisfied.

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

(65) ##STR00027##
wherein Met is a metal; (Y.sup.103-Y.sup.104) is a bidentate ligand, Y.sup.103 and Y.sup.104 are independently selected from C, N, O, P, and S; L.sup.101 is 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.

(66) In one aspect, the metal complexes are:

(67) ##STR00028##
wherein (O—N) is a bidentate ligand, having metal coordinated to atoms O and N.

(68) In another aspect, Met is selected from Ir and Pt. In a further aspect, (Y.sup.103-Y.sup.104) is a carbene ligand.

(69) Examples of organic compounds used as host are selected from the group consisting aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, azulene; group consisting 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 group consisting 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 atome, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Wherein each group is further substituted by a substituent selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

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

(71) ##STR00029## ##STR00030##
wherein R.sup.101 to R.sup.107 is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, 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. k is an integer from 0 to 20 or 1 to 20; k′″ is an integer from 0 to 20. X.sup.101 to X.sup.108 is selected from C (including CH) or N. Z.sup.101 and Z.sup.102 is selected from NR.sup.101, O, or S.
HBL:

(72) 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 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.

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

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

(75) ##STR00031##
wherein k is an integer from 1 to 20; L.sup.101 is an another ligand, k′ is an integer from 1 to 3.
ETL:

(76) 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.

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

(78) ##STR00032##
wherein R.sup.101 is selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, 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. Ar.sup.1 to Ar.sup.a has the similar definition as Ar's mentioned above. k is an integer from 1 to 20. X.sup.101 to X.sup.108 is selected from C (including CH) or N.

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

(80) ##STR00033##
wherein (O—N) or (N—N) is a bidentate ligand, having metal coordinated to atoms O, N or N, N; L.sup.101 is another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal.

(81) 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. encompasses undeuterated, partially deuterated, and fully deuterated versions thereof. Similarly, classes of substituents such as, without limitation, alkyl, aryl, cycloalkyl, heteroaryl, etc. also encompass undeuterated, partially deuterated, and fully deuterated versions thereof.

(82) In addition to and/or in combination with the materials disclosed herein, many hole injection materials, hole transporting materials, host materials, dopant materials, exiton/hole blocking layer materials, electron transporting and electron injecting materials may be used in an OLED. Non-limiting examples of the materials that may be used in an OLED in combination with materials disclosed herein are listed in Table 2 below. Table 2 lists non-limiting classes of materials, non-limiting examples of compounds for each class, and references that disclose the materials.

(83) TABLE-US-00001 TABLE 2 MATERIAL EXAMPLES OF MATERIAL PUBLICATIONS Hole injection materials Phthalocyanine and porphryin compounds Appl. Phys. Lett. 69, 2160 (1996) Starburst triarylamines J. Lumin. 72-74, 985 (1997) CF.sub.x Fluorohydrocarbon polymer Appl. Phys. Lett. 78, 673 (2001) Conducting polymers (e.g., PEDOT:PSS, polyaniline, polypthiophene) Synth. Met. 87, 171 (1997) WO2007002683 Phosphonic acid and sliane SAMs US20030162053 Triarylamine or polythiophene polymers with conductivity dopants EP1725079A1 0 Organic compounds with conductive inorganic compounds, such as molybdenum and tungsten oxides US20050123751 SID Symposium Digest, 37, 923 (2006) WO2009018009 n-type semiconducting organic complexes US20020158242 Metal organometallic complexes US20060240279 Cross-linkable compounds US20080220265 Polythiophene based polymers and copolymers WO 2011075644 EP2350216 Hole transporting materials Triarylamines Appl. Phys. Lett. 51, (e.g., TPD, α-NPD) 913 (1987) U.S. Pat. No. 5,061,569 EP650955 J. Mater. Chem. 3, 319 (1993) Appl. Phys. Lett. 90, 183503 (2007) Appl. Phys. Lett. 90, 183503 (2007) Triaylamine on spirofluorene core Synth. Met. 91, 209 (1997) Arylamine carbazole compounds 0 Adv. Mater. 6, 677 (1994), US20080124572 Triarylamine with (di)benzothiophene/ (di)benzofuran US20070278938, US20080106190 US20110163302 Indolocarbazoles Synth. Met. 111, 421 (2000) Isoindole compounds Chem. Mater. 15, 3148 (2003) Metal carbene complexes US20080018221 Phosphorescent OLED host materials Red hosts Arylcarbazoles Appl. Phys. Lett. 78, 1622 (2001) Metal 8-hydroxyquinolates (e.g., Alq.sub.3, BAlq) Nature 395, 151 (1998) US20060202194 WO2005014551 WO2006072002 Metal phenoxybenzothiazole compounds 0 Appl. Phys. Lett. 90, 123509 (2007) Conjugated oligomers and polymers (e.g., polyfluorene) Org. Electron. 1, 15 (2000) Aromatic fused rings WO2009066779, WO2009066778, WO2009063833, US20090045731, US20090045730, WO2009008311, US20090008605, US20090009065 Zinc complexes WO2010056066 Chrysene based compounds WO2011086863 Green hosts Arylcarbazoles Appl. Phys. Lett. 78, 1622 (2001) US20030175553 WO2001039234 Aryltriphenylene compounds US20060280965 US20060280965 0 WO2009021126 Poly-fused heteroaryl compounds US20090309488 US20090302743 US20100012931 Donor acceptor type molecules WO2008056746 WO2010107244 Aza-carbazole/DBT/DBF JP2008074939 US20100187984 Polymers (e.g., PVK) Appl. Phys. Lett. 77, 2280 (2000) Spirofluorene compounds WO2004093207 Metal phenoxybenzooxazole compounds WO2005089025 WO2006132173 0 JP200511610 Spirofluorene-carbazole compounds JP2007254297 JP2007254297 Indolocabazoles WO2007063796 WO2007063754 5-member ring electron deficient heterocycles (e.g., triazole, oxadiazole) J. Appl. Phys. 90, 5048 (2001) WO2004107822 Tetraphenylene complexes US20050112407 Metal phenoxypyridine compounds WO2005030900 Metal coordination complexes (e.g., Zn, Al with N{circumflex over ( )}N ligands) US20040137268, US20040137267 Blue hosts Arylcarbazoles 0 Appl. Phys. Lett, 82, 2422 (2003) US20070190359 Dibenzothiophene/ Dibenzofuran-carbazole compounds WO2006114966, US20090167162 US20090167162 WO2009086028 US20090030202, US20090017330 US20100084966 Silicon aryl compounds US20050238919 WO2009003898 Silicon/Germanium aryl compounds EP2034538A Aryl benzoyl ester 00 WO2006100298 Carbazole linked by non- conjugated groups 01 US20040115476 Aza-carbazoles 02 US20060121308 High triplet metal organometallic complex 03 U.S. Pat. No. 7,154,114 Phosphorescent dopants Red dopants Heavy metal porphyrins (e.g., PtOEP) 04 Nature 395, 151 (1998) Iridium(III) organometallic complexes 05 Appl. Phys. Lett. 78, 1622 (2001) 06 US2006835469 07 US2006835469 08 US20060202194 09 US20060202194 0 US20070087321 US20080261076 US20100090591 US20070087321 Adv. Mater. 19, 739 (2007) WO2009100991 WO2008101842 U.S. Pat. No. 7,232,618 Platinum(II) organometallic complexes WO2003040257 US20070103060 Osminum(III) complexes Chem. Mater. 17, 3532 (2005) Ruthenium(II) complexes 0 Adv. Mater. 17, 1059 (2005) Rhenium (I), (II), and (III) complexes US20050244673 Green dopants Iridium(III) organometallic complexes Inorg. Chem. 40, 1704 (2001) US20020034656 U.S. Pat. No. 7,332,232 US20090108737 WO2010028151 EP1841834B US20060127696 US20090039776 0 U.S. Pat. No. 6,921,915 US20100244004 U.S. Pat. No. 6,687,266 Chem. Mater. 16, 2480 (2004) US20070190359 US 20060008670 JP2007123392 WO2010086089, WO2011044988 Adv. Mater. 16, 2003 (2004) Angew. Chem. Int. Ed. 2006, 45, 7800 WO2009050290 0 US20090165846 US20080015355 US20010015432 US20100295032 Monomer for polymeric metal organometallic compounds U.S. Pat. No. 7,250,226, U.S. Pat. No. 7,396,598 Pt(II) organometallic complexes, including polydentated ligands Appl. Phys. Lett. 86, 153505 (2005) Appl. Phys. Lett. 86, 153505 (2005) Chem. Lett. 34, 592 (2005) WO2002015645 US20060263635 0 US20060182992 US20070103060 Cu complexes WO2009000673 US20070111026 Gold complexes Chem. Commun. 2906 (2005) Rhenium(III) complexes Inorg. Chem. 42, 1248 (2003) Osmium(II) complexes U.S. Pat. No. 7,279,704 Deuterated organometallic complexes US20030138657 Organometallic complexes with two or more metal centers US20030152802 U.S. Pat. No. 7,090,928 Blue dopants Iridium(III) organometallic complexes WO2002002714 0 WO2006009024 US20060251923 US20110057559 US20110204333 U.S. Pat. No. 7,393,599, WO2006056418, US20050260441, WO2005019373 U.S. Pat. No. 7,534,505 WO2011051404 U.S. Pat. No. 7,445,855 US20070190359, US20080297033 US20100148663 U.S. Pat. No. 7,338,722 US20020134984 Angew. Chem. Int. Ed. 47, 4542 (2008) 0 Chem. Mater. 18, 5119 (2006) Inorg. Chem. 46, 4308 (2007) WO2005123873 WO2005123873 WO2007004380 WO2006082742 Osmium(II) complexes U.S. Pat. No. 7,279,704 Organometallics 23, 3745 (2004) Gold complexes Appl. Phys. Lett. 74, 1361 (1999) Platinum(II) complexes WO2006098120, WO2006103874 Pt tetradentate complexes with at least one metal- carbene bond 0 U.S. Pat. No. 7,655,323 Exciton/hole blocking layer materials Bathocuprine compounds (e.g., BCP, BPhen) Appl. Phys. Lett. 75, 4 (1999) Appl. Phys. Lett. 79, 449 (2001) Metal 8-hydroxyquinolates (e.g., BAlq) Appl. Phys. Lett. 81, 162 (2002) 5-member ring electron deficient heterocycles such as triazole, oxadiazole, imidazole, benzoimidazole Appl. Phys. Lett. 81, 162 (2002) Triphenylene compounds US20050025993 Fluorinated aromatic compounds Appl. Phys. Lett. 79, 156 (2001) Phenothiazine-S-oxide WO2008132085 Silylated five-membered nitrogen, oxygen, sulfur or phosphorus dibenzoheterocycles WO2010079051 Aza-carbazoles US20060121308 Electron transporting materials Anthracene- benzoimidazole compounds 0 WO2003060956 US20090179554 Aza triphenylene derivatives US20090115316 Anthracene-benzothiazole compounds Appl. Phys. Lett. 89, 063504 (2006) Metal 8-hydroxyquinolates (e.g., Alq.sub.3, Zrq.sub.4) Appl. Phys. Lett. 51, 913 (1987) U.S. Pat. No. 7,230,107 Metal hydroxybenoquinolates Chem. Lett. 5, 905 (1993) Bathocuprine compounds such as BCP, BPhen, etc Appl. Phys. Lett. 91, 263503 (2007) Appl. Phys. Lett. 79, 449 (2001) 5-member ring electron deficient heterocycles (e.g., triazole, oxadiazole, imidazole, benzoimidazole) Appl. Phys. Lett. 74, 865 (1999) Appl. Phys. Lett. 55, 1489 (1989) 00 Jpn. J. Apply. Phys. 32, L917 (1993) Silole compounds 01 Org. Electron. 4, 113 (2003) Arylborane compounds 02 J. Am. Chem. 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EXPERIMENTAL

Material Synthesis

(84) All reactions were carried out under nitrogen protections unless specified otherwise. All solvents for reactions are anhydrous and used as received from commercial sources.

Synthesis of Compound 1

(85) ##STR00207##

Synthesis of 2-(3-((dichlorophosphino)oxy)phenyl)-1-(2,6-diisopropylphenyl)-1H-imidazole

(86) A 100 mL round-bottomed flask was charged with 3-(1-(2,6-diisopropylphenyl)-1H-imidazol-2-yl)phenol (0.309 g, 0.964 mmol), trichlorophosphine (0.3 ml, 3.44 mmol) and 30 ml of dichloromethane. A solution of triethylamine (0.135 ml, 0.964 mmol) in 60 ml of dichloromethane was added dropwise at −20° C. for a period of 1 hr. The reaction mixture was then stirred for 16 hrs. The reaction mixture was used for the next step without purification.

(87) ##STR00208##

Synthesis of 3-(1-(2,6-diisopropylphenyl)-1H-imidazol-2-yl)phenyl bis(2,6-dimethylphenyl)phosphite

(88) A solution of 2,6-dimethylphenol (1.413 g, 11.56 mmol), triethylamine (1.614 ml, 11.56 mmol) and dichloromethane (20 ml) was added dropwise to the reaction mixture from the previous step at 0° C. The reaction mixture was then stirred at room temperature for 2.5 hrs. The reaction mixture was then filtered and the filtrate was subjected to column chromatography (SiO.sub.2, 100% DCM to 20% ETOAC in DCM) to yield the desired product, 3-(1-(2,6-diisopropylphenyl)-1H-imidazol-2-yl)phenyl bis(2,6-dimethylphenyl)phosphite. (0.338 g, 59%).

(89) ##STR00209##

Synthesis of OsH4(PPh3)3

(90) A 500 mL round-bottomed flask was charged with triphenylphosphine (15.74 g, 60.0 mmol) and ethanol (Volume: 400 ml) to give a colorless solution. The reaction mixture was heated to reflux, then (NH.sub.4).sub.2OsCl.sub.6(4.39 g, 10.00 mmol) was added in one portion. A solution of NaBH.sub.4 (2.001 g, 52.9 mmol) in 300 ml of ethanol was added dropwise to the reaction mixture for a period of 10 mins. The reaction mixture was heated to reflux for another 15 mins. The reaction mixture was then cooled down. The solid was filtered and washed in sequence with ethanol, water, ethanol, and hexane to yield the desired product, OsH.sub.4(PPh.sub.3).sub.3. (8.32 g, 85%).

Synthesis of Compound 1

(91) A 100 mL round-bottomed flask was charged with 3-(1-(2,6-diisopropylphenyl)-1H-imidazol-2-yl)phenyl bis(2,6-dimethylphenyl)phosphite (0.334 g, 0.564 mmol), OsH.sub.4(PPh.sub.3).sub.3(0.240 g, 0.245 mmol) in decahydronaphthalene (Volume: 5 ml) to give a white suspension. The reaction mixture was heated to 200° C. for 1.5 hr. The solvent was removed by vacuum distillation and the residue was subjected to column chromatography (SiO.sub.2, 15% etoac to 20% etoac in heptane) to yield Compound 1. (0.178 g, 53%).

Synthesis of Compound 2

(92) ##STR00210##

Synthesis of 1-([1,1′:3′,1″-terphenyl]-2′-yl)-2-(3-((diphenylphosphino)oxy)-5-methylphenyl)-1H-imidazole

(93) A 250 mL round-bottomed flask was charged with 3-(1-([1,1′:3′,1″-terphenyl]-2′-yl)-1H-imidazol-2-yl)-5-methylphenol (0.406 g, 1.009 mmol), chlorodiphenylphosphine (0.186 ml, 1.009 mmol), triethylamine (0.672 ml, 4.81 mmol) and toluene (Volume: 70 ml) to give a brown solution. The reaction mixture was heated to 90° C. for 16 hrs. The reaction mixture was filtered and the filtrate was subjected to column chromatography (SiO2, 35% etoac to 50% etoac in heptane) to yield the desired product, 1-([1,1′:3′,1″-terphenyl]-2′-yl)-2-(3-((diphenylphosphino)oxy)-5-methylphenyl)-1H-imidazole. (0.395 g, 66%).

(94) ##STR00211##

Synthesis of Compound 2

(95) A 100 mL round-bottomed flask was charged with 1-([1,1′:3′,1″-terphenyl]-2′-yl)-2-(3-((diphenylphosphino)oxy)-5-methylphenyl)-1H-imidazole (0.388 g, 0.66 mmol), OsH.sub.4(PPh.sub.3).sub.3(0.28 g, 0.288 mmol) and decahydronaphthalene (Volume: 6 ml) to give a white suspension. The reaction mixture was heated to 200° C. for 1.5 hr. The solvent was removed by vacuum distillation and the residue was subjected to column chromatography (SiO.sub.2, 15% etoac to 20% etoac in heptane) to yield Compound 2. (0.34 g, 89%).

Synthesis of Compound 3

(96) ##STR00212##

Synthesis of 2-((dichlorophosphino)oxy)-6-phenylpyridine

(97) A 100 mL round-bottomed flask was charged with 6-phenylpyridin-2-ol (0.814 g, 4.75 mmol), trichlorophosphine (1.245 ml, 14.26 mmol) and CH.sub.2Cl.sub.2 (Volume: 120 ml) to give a white suspension. A solution of triethylamine (0.664 ml, 4.75 mmol) in 60 ml of dichloromethane was added dropwise at −20° C. for a period of 1 hr. The reaction mixture was then stirred for 16 hrs. The reaction mixture was used for next step without purification.

(98) ##STR00213##

Synthesis of bis(2,6-dimethylphenyl) (6-phenylpyridin-2-yl)phosphite

(99) A solution of 2,6-dimethylphenol (8.13 g, 66.6 mmol), triethylamine (9.29 ml, 66.6 mmol) and dichloromethane (20 ml) was added dropwise to the reaction mixture from the previous step at 0° C. The reaction mixture was then stirred at room temperature for 2.5 hrs. The reaction mixture was then filtered and the filtrate was subjected to column chromatography (SiO.sub.2, 3% etoac in heptane to 5% etoac in heptane) to yield the desired product, bis(2,6-dimethylphenyl) (6-phenylpyridin-2-yl)phosphite. (1.17 g, 55%).

(100) ##STR00214##

Synthesis of Compound 3

(101) A 100 mL round-bottomed flask was charged with (0.388 g, 0.66 mmol) bis(2,6-dimethylphenyl) (6-phenylpyridin-2-yl)phosphite, OsH.sub.4(PPh.sub.3).sub.3(1.939 g, 1.976 mmol) and decahydronaphthalene (Volume: 40 ml) to give a white suspension. The reaction mixture was heated to 200° C. for 1.5 hrs. The solvent was removed by vacuum distillation and residue was subjected to column chromatography (SiO.sub.2, 10% etoac in heptane) to yield Compound 3. (0.95 g, 45%).

Device Test Data

Device Examples

(102) All example devices were fabricated by high vacuum (<10.sup.−7 Torr) thermal evaporation. The anode electrode consisted of 1200 Å of indium tin oxide (ITO). The cathode consisted of 10 Å of LiF followed by 1,000 Å of Al. All devices were encapsulated with a glass lid sealed with an epoxy resin in a nitrogen glove box (<1 ppm of H.sub.2O and O.sub.2) immediately after fabrication, and a moisture getter was incorporated inside the package.

(103) The organic stack of the device examples consisted of sequentially, from the ITO surface, 100 Å of LG101 (purchased from LG Chemical) as the hole injection layer (HIL), 400 Å of 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (alpha-NPD) as the hole transporting layer (HTL), 300 Å of the invention compound, Compound 3, doped in Compound A as host with 15 weight percent of an osmium phosphorescent compound as the emissive layer (EML), a 50 Å of Compound A as electron blocking layer (EBL), 300 Å of LG201 (purchased from LG Chemical) as the electron transporting layer (ETL). The resulting device data from those device examples is summarized in Table 2 below. As used herein, NPD and Compound A have the following structures:

(104) ##STR00215##

(105) TABLE-US-00002 TABLE 2 Device Data λ.sub.max FWHM Voltage LE EQE PE x y (nm) (nm) (V) (Cd/A) (%) (lm/W) Inventive 0.397 0.568 548 92 6.7 19.4 5.8 9.1 Example 1 Compound 3

(106) In the novel compound disclosed herein, the electron withdrawing ability of phosphine/phosphite is used to lower the HOMO of osmium complexes to be more comparable to iridium based dopants. The oxidation potential values of the compounds provided in Table 3 below demonstrates this point.

(107) TABLE-US-00003 TABLE 3 Oxidation potentials and the calculated HOMO level of the bis(tridenate) osmium complexes Experimental HOMO level Oxidation Structure by calculation* potential** Example 1 (from US 2005/0260449) −4.32 V −0.5 V Example 2 (from WO 2009046266) −4.63 V −0.35 V Compound 1 −5.04 V 0.12 V Compound 3 −5.36 V 0.3 V Example 3 0 −3.44 V −1.2 V*** Example 4 −4.52 V −0.4 V*** *DFT (density function theory) calculation using Gaussian/B3lyp/cep-31g **Oxidation potential was referred to the anodic and cathodic peak potentials referenced to the Fc.sup.+/Fc couple in V. ***extrapolated oxidation potential from Graph 1 shown in FIG. 5.
Graph 1 shows a correlation between calculated HOMO level and oxidation potential (measured by cyclic voltammetry).

(108) Osmium (II) complexes have been investigated for OLED applications. (see review: Eur. J. Inorg. Chem. 2006, 3319-3332). The octahedral ligand arrangement of the Os(II) complexes resembles that of Ir(III) complexes. Os(II) complexes generally exhibit low oxidation potential, i.e. shallow HOMO energy level than Ir(III) complexes. For example, the Examples 1 and 2 in US 2005026049 and WO 2009046266, respectively, show oxidation potential of −0.5V and −0.35V; in contrast with the oxidation potential of 0.3V of Ir(PPY)3. The extremely shallow HOMO level of Osmium bis(tridenate) complexes make it difficult to fit in the main stream oled device structure. According to the invention disclosed in the present disclosure, by taking advantage of the electron withdrawing ability of the phosphine/phosphite; the inventors firmed Osmium bis(tridenate) complexes having more reasonable HOMO levels. i.e. oxidation potential between 0 to 0.3V. For example, comparing Example 3 and Compound 1; the oxidation potential changed from −1.2V to 0.12V by replacing imidazole ring with phosphite group. Similarly, comparing Example 4 and Compound 3, the oxidation potential changed from −0.4V to 0.3V by replacing a pyridine ring with a phosphite group. Moreover, phosphine moiety is part of tridenate frame. The rigid nature of the tridentate ligands generally results in narrow emission line widths and short excited state lifetimes, which can result in better color purity and longer device lifetime, making them suitable for display applications.

(109) 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.