Patent Application
20160218303
The claimed invention was made by, on behalf of, and/or in connection with one or more of the following parties to a joint university corporation research agreement: The Regents of the University of Michigan, Princeton University, University of Southern California, and Universal Display Corporation. The agreement was in effect on and before the date the claimed invention was made, and the claimed invention was made as a result of activities undertaken within the scope of the agreement.
The present invention relates to compounds for use as emitters and devices, such as organic light emitting diodes, including the same.
Opto-electronic devices that make use of organic materials are becoming increasingly desirable for a number of reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials. For example, the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.
OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, illumination, and backlighting. Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.
One application for phosphorescent emissive molecules is a full color display. Industry standards for such a display call for pixels adapted to emit particular colors, referred to as “saturated” colors. In particular, these standards call for saturated red, green, and blue pixels. Color may be measured using CIE coordinates, which are well known to the art.
One example of a green emissive molecule is tris(2-phenylpyridine) iridium, denoted Ir(ppy)3, which has the following structure:
In this, and later figures herein, we depict the dative bond from nitrogen to metal (here, Ir) as a straight line.
As used herein, the term “organic” includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices. “Small molecule” refers to any organic material that is not a polymer, and “small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances. For example, using a long chain alkyl group as a substituent does not remove a molecule from the “small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter. A dendrimer may be a “small molecule,” and it is believed that all dendrimers currently used in the field of OLEDs are small molecules.
As used herein, “top” means furthest away from the substrate, while “bottom” means closest to the substrate. Where a first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is “in contact with” the second layer. For example, a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.
As used herein, “solution processible” means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.
A ligand may be referred to as “photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material. A ligand may be referred to as “ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.
As used herein, and as would be generally understood by one skilled in the art, a first “Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is “greater than” or “higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative). On a conventional energy level diagram, with the vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. A “higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a “lower” HOMO or LUMO energy level.
As used herein, and as would be generally understood by one skilled in the art, a first work function is “greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a “higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.
More details on OLEDs, and the definitions described above, can be found in U.S. Pat. No. 7,279,704, which is incorporated herein by reference in its entirety.
According to an aspect of the present disclosure, a new compound is disclosed. The compound comprises a carbene ligand LA selected from the group consisting of:
wherein X1 is CRc2 or N, X2 is CRc3 or N;
wherein Ra1, Ra2, Rb1, Rb2, Rb3, Rb4, Rc1, Rc2, Rc3, Rc4, R1 and R2 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, haloalkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, thioalkoxy, aryloxy, thioaryloxy, amino, silyl, halosilyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, NCO, NCS, OCN, SCN, OCmF2m+1 or SCmF2m+1, and combinations thereof;
wherein at least one of R1, Ra1, Ra2, Rc1, Rc3, and Rc4 comprises an acceptor group selected from the group consisting of CN, F directly attached to an aromatic ring, SimF2m+1, NCO, NCS, OCN, SCN, OCmF2m+1 and SCmF2m+1, where m≧1;
wherein any adjacent substituents of Rb1, Rb2, Rb3, and Rb4 are optionally joined or fused into a ring;
wherein the ligand LA is coordinated to a metal M; and
wherein the ligand LA is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
According to another aspect of the present disclosure, an organic light emitting device (OLED) is disclosed. The OLED can include an anode, and an organic layer, disposed between the anode and the cathode. The organic layer comprises a first compound comprising a carbene ligand LA selected from the group consisting of:
wherein X1 is CR2 or N, X2 is CRc3 or N;
wherein Ra1, Ra2, Rb1, Rb2, Rb3, Rb4, Rc1, Rc2, Rc3, Rc4, R1 and R2 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, haloalkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, thioalkoxy, aryloxy, thioaryloxy, amino, silyl, halosilyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, NCO, NCS, OCN, SCN, OCmF2m+1 or SCmF2m+1, and combinations thereof;
wherein at least one of R1, Ra1, Ra2, Rc1, Rc3, and Rc4 comprises an acceptor group selected from the group consisting of CN, F directly attached to an aromatic ring, SimF2m+1, NCO, NCS, OCN, SCN, OCmF2m+1 and SCmF2m+1, where m≧1;
wherein any adjacent substituents of Rb1, Rb2, Rb3, and Rb4 are optionally joined or fused into a ring;
wherein the ligand LA is coordinated to a metal M; and
wherein the ligand LA is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
According to yet another aspect of the present disclosure, a formulation comprising the first compound is disclosed.
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.
The initial OLEDs used emissive molecules that emitted light from their singlet states (“fluorescence”) as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.
More recently, OLEDs having emissive materials that emit light from triplet states (“phosphorescence”) have been demonstrated. Baldo et al., “Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices,” Nature, vol. 395, 151-154, 1998; (“Baldo-I”) and Baldo et al., “Very high-efficiency green organic light-emitting devices based on electrophosphorescence,” Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999) (“Baldo-II”), 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.
More examples for each of these layers are available. For example, a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety. An example of a p-doped hole transport layer is m-MTDATA doped with F4-TCNQ at a molar ratio of 50:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which is incorporated by reference in its entirety. An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entireties, disclose examples of cathodes including compound cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electrically-conductive, sputter-deposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Patent Application Publication No. 2003/0230980, which are incorporated by reference in their entireties. Examples of injection layers are provided in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of protective layers may be found in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety.
The simple layered structure illustrated in
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
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 processibility than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize. Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.
Devices fabricated in accordance with embodiments of the present 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.
Devices fabricated in accordance with embodiments of the invention can be incorporated into a wide variety of electronic component modules (or units) that can be incorporated into a variety of electronic products or intermediate components. Examples of such electronic products or intermediate components include display screens, lighting devices such as discrete light source devices or lighting panels, etc. that can be utilized by the end-user product manufacturers. Such electronic component modules can optionally include the driving electronics and/or power source(s). Devices fabricated in accordance with embodiments of the invention can be incorporated into a wide variety of consumer products that have one or more of the electronic component modules (or units) incorporated therein. Such consumer products would include any kind of products that include one or more light source(s) and/or one or more of some type of visual displays. Some examples of such consumer products include flat panel displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, laser printers, telephones, cell phones, tablets, phablets, 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.
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.
The term “halo,” “halogen,” or “halide” as used herein includes fluorine, chlorine, bromine, and iodine.
The term “alkyl” as used herein contemplates both straight and branched chain alkyl radicals. Preferred alkyl groups are those containing from one to fifteen carbon atoms and includes methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, and the like. Additionally, the alkyl group may be optionally substituted.
The term “cycloalkyl” as used herein contemplates cyclic alkyl radicals. Preferred cycloalkyl groups are those containing 3 to 7 carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, and the like. Additionally, the cycloalkyl group may be optionally substituted.
The term “alkenyl” as used herein contemplates both straight and branched chain alkene radicals. Preferred alkenyl groups are those containing two to fifteen carbon atoms. Additionally, the alkenyl group may be optionally substituted.
The term “alkynyl” as used herein contemplates both straight and branched chain alkyne radicals. Preferred alkynyl groups are those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted.
The terms “aralkyl” or “arylalkyl” as used herein are used interchangeably and contemplate an alkyl group that has as a substituent an aromatic group. Additionally, the aralkyl group may be optionally substituted.
The term “heterocyclic group” as used herein contemplates aromatic and non-aromatic cyclic radicals. Hetero-aromatic cyclic radicals also means heteroaryl. Preferred hetero-non-aromatic cyclic groups are those containing 3 or 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperdino, pyrrolidino, and the like, and cyclic ethers, such as tetrahydrofuran, tetrahydropyran, and the like. Additionally, the heterocyclic group may be optionally substituted.
The term “aryl” or “aromatic group” as used herein contemplates single-ring groups and polycyclic ring systems. The polycyclic rings may have two or more rings in which two carbons are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is aromatic, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Additionally, the aryl group may be optionally substituted.
The term “heteroaryl” as used herein contemplates single-ring hetero-aromatic groups that may include from one to three heteroatoms, for example, pyrrole, furan, thiophene, imidazole, oxazole, thiazole, triazole, pyrazole, pyridine, pyrazine and pyrimidine, and the like. The term heteroaryl also includes polycyclic hetero-aromatic systems having two or more rings in which two atoms are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Additionally, the heteroaryl group may be optionally substituted.
The alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, heterocyclic group, aryl, and heteroaryl may be optionally substituted with one or more substituents selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
As used herein, “substituted” indicates that a substituent other than H is bonded to the relevant position, such as carbon. Thus, for example, where R1 is mono-substituted, then one R1 must be other than H. Similarly, where R1 is di-substituted, then two of R1 must be other than H. Similarly, where R1 is unsubstituted, R1 is hydrogen for all available positions.
The “aza” designation in the fragments described herein, i.e. aza-dibenzofuran, aza-dibenzothiophene, etc. means that one or more of the C—H groups in the respective fragment can be replaced by a nitrogen atom, for example, and without any limitation, azatriphenylene encompasses both dibenzo[f,h]quinoxaline and dibenzo[f,h]quinoline. One of ordinary skill in the art can readily envision other nitrogen analogs of the aza-derivatives described above, and all such analogs are intended to be encompassed by the terms as set forth herein.
It is to be understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. phenyl, phenylene, naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g. benzene, naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent.
According to an aspect of the present disclosure, a new compound is disclosed. The compound comprises a carbene ligand LA selected from the group consisting of:
wherein X1 is CRc2 or N, X2 is CR3 or N;
wherein Ra1, Ra2, Rb1, Rb2, Rb3, Rb4, Rc1, Rc2, Rc3, Rc4, R1 and R2 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, haloalkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, thioalkoxy, aryloxy, thioaryloxy, amino, silyl, halosilyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, NCO, NCS, OCN, SCN, OCmF2m+1 or SCmF2m+1, and combinations thereof;
wherein at least one of R1, Ra1, Ra2, Rc1, Rc3, and Rc4 comprises an acceptor group selected from the group consisting of CN, F directly attached to an aromatic ring, SimF2m+1, NCO, NCS, OCN, SCN, OCmF2m+1 and SCmF2m+1, where m≧1;
wherein any adjacent substituents of Rb1, Rb2, Rb3, and Rb4 are optionally joined or fused into a ring;
wherein the ligand LA is coordinated to a metal M; and
wherein the ligand LA is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
In some embodiments of the compound, M can be selected from the group consisting of Ir, Rh, Re, Ru, Os, Pt, Au, and Cu. In some embodiments, M is Ir or Pt.
The compound can be homoleptic or heteroleptic.
In some embodiments of the compound, X1 is CRc2, and X2 is CRc3.
In other embodiments of the compound, X1 is CRc2, and X2 is N.
In other embodiments of the compound, X1 is N, and X2 is CR3.
In other embodiments of the compound, X1 is N, and X2 is N.
In some embodiments of the compound, at least one of R1, Ra1, Ra2, Rc1, Rc3, and Rc4 comprises a CN group.
In some embodiments of the compound, at least one of Ra1, Ra2, Rc1, Rc3, and Rc4 is CN.
In other embodiments of the compound, R1 and R2 are each independently selected from the group consisting of alkyl or cycloalkyl.
In other embodiments of the compound, R1 and R2 are each independently selected from the group consisting of aryl, substituted aryl, heteroaryl, and substituted heteroaryl.
In some other embodiments of the compound, the ligand LA is selected from the group consisting of:
According to another aspect of the present disclosure, the compound has a formula of M(LA)n(LB)m-n; wherein M is Ir or Pt; LB is a bidentate ligand; and wherein when M is Ir, m is 3, and n is 1, 2, or 3; and when M is Pt, m is 2, and n is 1 or 2.
In some embodiments of the compound having the formula of M(LA)n(LB)m-n, the compound has a formula of Ir(LA)3.
In some embodiments of the compound having the formula of M(LA)n(LB)m-n, the compound has a formula of Ir(LA)(LB)2; and wherein LB is different from LA.
In some embodiments of the compound having the formula of M(LA)n(LB)m-n, the compound has a formula of Ir(LA)2(LB); and wherein LB is different from LA.
In some embodiments of the compound having the formula of M(LA)n(LB)m-n, the compound has a formula of Pt(LA)(LB); and wherein LA and LB can be same or different. LA and LB can be connected to form a tetradentate ligand. In some embodiments, LA and LB are connected at two places to form a marcrocyclic tetradentate ligand.
In some embodiments of the compound having the formula of M(LA)n(LB)m-n, LB is selected from the group consisting of:
wherein each X1 to X13 are independently selected from the group consisting of carbon and nitrogen;
wherein X is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO2, CR′R″, SiR′R″, and GeR′R″,
wherein R′ and R″ are optionally fused or joined to form a ring;
wherein each Ra, Rb, Rd, and Rd may represent from mono substitution to the possible maximum number of substitution, or no substitution;
wherein R′, R″, Ra, Rb, Rc, and Rd are each 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; and
wherein any two adjacent substitutents of Ra, Rb, Rc, and Rd are optionally fused or joined to form a ring or form a multidentate ligand.
In some embodiments of the compound having the formula of M(LA)n(LB)m-n, LB is selected from the group consisting of:
In some embodiments of the compound having the formula of M(LA)n(LB)m-n, LB is selected from the group consisting of:
In the embodiments of the compound where the ligand LA is selected from the group consisting of LA1 through LA273, the compound is Compound Ax having the formula Ir(LAi)3; and wherein x=i; i is an integer from 1 to 273.
In other embodiments of the compound where the ligand LA is selected from the group consisting of LA1 through LA273, the compound is the Compound By having the formula Ir(LAi)(LBj)2 or Compound Cz having the formula Ir(LAi)2(LBj);
wherein y=55i+j−55; i is an integer from 1 to 273, and j is an integer from 1 to 55;
wherein z=55i+j−55; i is an integer from 1 to 273, and j is an integer from 1 to 55; and
wherein LB1 to LB55 have the structures as defined above.
According to another aspect of the present disclosure, an organic light emitting device (OLED) is disclosed. The OLED can include an anode, and an organic layer, disposed between the anode and the cathode. The organic layer comprises a first compound comprising a carbene ligand LA selected from the group consisting of:
wherein X1 is CRc2 or N, X2 is CRc3 or N;
wherein Ra1, Ra2, Rb1, Rb2, Rb3, Rb4, Rc1, Rc2, Rc3, Rc4, R1 and R2 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, haloalkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, thioalkoxy, aryloxy, thioaryloxy, amino, silyl, halosilyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, NCO, NCS, OCN, SCN, OCmF2m+1 or SCmF2m+1, and combinations thereof;
wherein any adjacent substituents of Rb1, Rb2, Rb3, and Rb4 are optionally joined or fused into a ring;
wherein the ligand LA is coordinated to a metal M; and
wherein the ligand LA is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
In some embodiments of the OLED, the first compound can be an emissive dopant. In some embodiments, the compound can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence), triplet-triplet annihilation, or combinations of these processes.
The first organic light emitting device can be incorporated into a device selected from the group consisting of a consumer product, an electronic component module, and a lighting panel. The organic layer can be an emissive layer and the compound can be an emissive dopant in some embodiments, while the compound can be a non-emissive dopant in other embodiments.
The organic layer can also include a host. In some embodiments, the host can include a metal complex. The host can be a triphenylene containing benzo-fused thiophene or benzo-fused furan. Any substituent in the host can be an unfused substituent independently selected from the group consisting of CnH2n+1, OCnH2n+1, OAr1, N(CnH2n+1)2, N(Ar1)(Ar2), CH═CH—CnH2n+1, C≡C—CnH2n+1, Ar1, Ar1—Ar2, and CnH2n—Ar1, or no substitution. In the preceding substituents n can range from 1 to 10; and Ar1 and Ar2 can be independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.
The host can be a compound comprising at least one chemical group selected from the group consisting of triphenylene, tetraphenylene, carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene. The host can include a metal complex. The host can be a specific compound selected from the group consisting of:
and combinations thereof.
In yet another aspect of the present disclosure, a formulation comprising the compound comprising a carbene ligand LA selected from the group consisting of:
is disclosed;
wherein X1 is CRc2 or N, X2 is CRc3 or N;
wherein Ra1, Ra2, Rb1, Rb2, Rb3, Rb4, Rc1, Rc2, Rc3, Rc4, R1 and R2 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, haloalkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, thioalkoxy, aryloxy, thioaryloxy, amino, silyl, halosilyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, NCO, NCS, OCN, SCN, OCmF2m+1 or SCmF2m+1, and combinations thereof;
wherein at least one of R1, Ra1, Ra2, Rc1, Rc3, and Rc4 comprises an acceptor group selected from the group consisting of CN, F directly attached to an aromatic ring, SimF2m+1, NCO, NCS, OCN, SCN, OCmF2m+1 and SCmF2m+1, where m≧1;
wherein any adjacent substituents of Rb1, Rb2, Rb3, and Rb4 are optionally joined or fused into a ring;
wherein the ligand LA is coordinated to a metal M; and
wherein the ligand LA is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
Combination with Other Materials
The materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device. For example, emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present. The materials described or referred to below are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.
A 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 are not limited to: a phthalocyanine or porphyrin derivative; an aromatic amine derivative; an indolocarbazole derivative; a polymer containing fluorohydrocarbon; a polymer with conductivity dopants; a conducting polymer, such as PEDOT/PSS; a self-assembly monomer derived from compounds such as phosphonic acid and silane derivatives; a metal oxide derivative, such as MoOx; a p-type semiconducting organic compound, such as 1,4,5,8,9,12-Hexaazatriphenylenehexacarbonitrile; a metal complex, and a cross-linkable compound.
Examples of aromatic amine derivatives used in HIL or HTL include, but are not limited to the following general structures:
Each of Ar1 to Ar9 is selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. 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.
In one aspect, Ar1 to Ar9 is independently selected from the group consisting of:
wherein k is an integer from 1 to 20; X101 to X108 is C (including CH) or N; Z101 is NAr1, O, or S; Ar1 has the same group defined above.
Examples of metal complexes used in HIL or HTL include, but are not limited to the following general formula:
wherein Met is a metal, which can have an atomic weight greater than 40; (Y101-Y102) is a bidentate ligand, Y101 and Y102 are independently selected from C, N, O, P, and S; L101 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.
In one aspect, (Y101-Y102) is a 2-phenylpyridine derivative. In another aspect, (Y101-Y102) is a carbene ligand. In another aspect, Met is selected from Ir, Pt, Os, and Zn. In a further aspect, the metal complex has a smallest oxidation potential in solution vs. Fc+/Fc couple less than about 0.6 V.
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.
Examples of metal complexes used as host are preferred to have the following general formula:
wherein Met is a metal; (Y103-Y104) is a bidentate ligand. Y103 and Y104 are independently selected from C, N, O, P, and S; L101 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.
In one aspect, the metal complexes are:
wherein (O—N) is a bidentate ligand, having metal coordinated to atoms O and N.
In another aspect, Met is selected from Ir and Pt. In a further aspect, (Y103-Y104) is a carbene ligand.
Examples of organic compounds used as host are selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. 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.
In one aspect, the host compound contains at least one of the following groups in the molecule:
wherein R101 to R107 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. X101 to X108 is selected from C (including CH) or N. Z101 and Z102 is selected from NR101, O, or S.
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.
In one aspect, compound used in HBL contains the same molecule or the same functional groups used as host described above.
In another aspect, compound used in HBL contains at least one of the following groups in the molecule:
wherein k is an integer from 1 to 20; L101 is an another ligand, k′ is an integer from 1 to 3.
Electron transport layer (ETL) may include a material capable of transporting electrons. Electron transport layer may be intrinsic (undoped), or doped. Doping may be used to enhance conductivity. Examples of the ETL material are not particularly limited, and any metal complexes or organic compounds may be used as long as they are typically used to transport electrons.
In one aspect, compound used in ETL contains at least one of the following groups in the molecule:
wherein R101 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. Ar1 to Ar3 has the similar definition as Ar's mentioned above. k is an integer from 1 to 20. X101 to X108 is selected from C (including CH) or N.
In another aspect, the metal complexes used in ETL include, but are not limited to the following general formula:
wherein (O—N) or (N—N) is a bidentate ligand, having metal coordinated to atoms O, N or N, N; L101 is another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal.
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.
In addition to and/or in combination with the materials disclosed herein, many hole injection materials, hole transporting materials, host materials, dopant materials, exciton/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 A below. Table A lists non-limiting classes of materials, non-limiting examples of compounds for each class, and references that disclose the materials.
To a stirred solution of 1H-imidazole-5-carbaldehyde (10 g, 104 mmol) in DMF (135 mL), iodobenzene (31.8 g, 156 mmol), cyclohexane-1,2-diamine (2.377 g, 20.8 mmol), cesium carbonate (67.8 g, 208 mmol), and copper(I) iodide (0.991 g, 5.2 mmol) were added. The reaction mixture was stirred at 110° C. for about 16 hours. It was precipitated in water and filtered. The residue was column chromatographed with THF:hexane (1:4). 1-Phenyl-1H-imidazole-4-carbaldehyde (3.5 g, 20.3 mmol, 19.5% yield) was isolated as white solid.
To a stirred solution of 1-phenyl-1H-imidazole-4-carbaldehyde (3.5 g, 20.3 mmol) in THF (60 mL), ammonium hydroxide (22 mL, 224 mmol) was added. Iodine (15.48 g, 61.0 mmol) was added in portions at room temperature. The reaction was monitored with HPLC for the completion of the reaction. Diethyl ether and saturated sodium thiosulphate were added. The organic layer was separated, dried and column chromatographed with THF:hexane (1:4) yielded 1-phenyl-1H-imidazole-4-carbonitrile (3.1 g, 18.3 mmol, 90% yield).
To a stirred solution of 1-phenyl-1H-imidazole-4-carbonitrile (1.6 g, 9.5 mmol) in DCM (25 mL), methyl trifluoromethanesulfonate (1.7 g, 10.4 mmol) was added and stirred at room temperature for 4 hours. The precipitate was filtered and washed with DCM yielded 4-cyano-3-methyl-1-phenyl-1H-imidazol-3-ium trifluoromethanesulfonate (3.0 g, 9.0 mmol, 95% yield).
1H-imidazole-5-carbaldehyde (10.0 g, 104 mmol), 1-iodo-3-methylbenzene (34.0 g, 156 mmol), cyclohexane-1,2-diamine (2.4 g, 20.8 mmol), cesium carbonate (67.8 g, 208 mmol), and copper(I) iodide (0.991 g, 5.2 mmol) were stirred in DMF (135 mL) at 110° C. for 3 days. The reaction mixture was precipitated in water and filtered. The residue was column chromatographed with THF:hexane (1:4) yielded a mixture of 1-(m-tolyl)-1H-imidazole-4-carbaldehyde and 1-(m-tolyl)-1H-imidazole-5-carbaldehyde (19.0 g) were used for next step without further purification.
To a stirred solution of mixture of 1-(m-tolyl)-1H-imidazole-4-carbaldehyde and 1-(m-tolyl)-1H-imidazole-5-carbaldehyde (15 g, 80.6 mmol) in THF (100 mL), ammonium hydroxide (47 mL, 403 mmol) was added. Iodine (30.7 g, 121 mmol) was added in portions at room temperature. The reaction was monitored with HPLC for the completion of the reaction. Ether and saturated sodium thiosulphate were added. The organic layer was separated, dried and column chromatographed with EA:hexane (1:3) yielded 1-(m-tolyl)-1H-imidazole-5-carbonitrile (4.0 g, 21.8 mmol, 27% yield) and 1-(m-tolyl)-1H-imidazole-4-carbonitrile (4.9 g, 26.7 mmol, 33% yield).
To a stirred solution of 1-(m-tolyl)-1H-imidazole-4-carbonitrile (2.0 g, 10.9 mmol) in DCM (30 mL), methyl trifluoromethanesulfonate (2.0 g, 12.0 mmol) was added and stirred at room temperature for 4 hours. The precipitate was filtered and washed with diethyl ether yielded 4-cyano-3-methyl-1-(m-tolyl)-1H-imidazol-3-ium trifluoromethanesulfonate (3.4 g, 9.8 mmol, 90% yield).
To a stirred solution of 1-(m-tolyl)-1H-imidazole-5-carbonitrile (2 g, 10.9 mmol) in DCM (30 mL), methyl trifluoromethanesulfonate (1.8 g, 10.9 mmol) was added and stirred at room temperature for 4 hours. The precipitate was filtered and washed with diethyl ether yielded 5-cyano-3-methyl-1-(m-tolyl)-1H-imidazol-3-ium trifluoromethanesulfonate (3.2 g, 9.2 mmol, 84% yield).
To a stirred solution of 1H-imidazole-5-carbaldehyde (10 g 104 mmol) in DMF (135 mL), 1-iodo-3,5-dimethylbenzene (18 mL, 125 mmol), cyclohexane-1,2-diamine (2.5 mL, 20.8 mmol), cesium carbonate (67.8 g, 208 mmol), copper(I) iodide (0.991 g, 5.2 mmol) were added. The solution mixture was stirred at 110° C. for about 16 hours. The reaction was precipitated in water and filtered. The residue was column chromatographed with THF:hexane (1:4). The crude (a mixture of 1-(3,5-dimethylphenyl)-1H-imidazole-4-carbaldehyde and 1-(3,5-dimethylphenyl)-1H-imidazole-5-carbaldehyde, 18 g) was used for next step without further purification.
To a stirred solution of a mixture of 15.0 g of 1-(3,5-dimethylphenyl)-1H-imidazole-4-carbaldehyde and 1-(3,5-dimethylphenyl)-1H-imidazole-5-carbaldehyde in THF (88 mL), ammonium hydroxide (44 mL, 375 mmol) was added. Iodine (28.5 g, 112 mmol) was added in portions at room temperature. The reaction was monitored with HPLC for the completion of the reaction. Ether and saturated sodium thiosulphate were added. The organic layer was separated, dried and column chromatographed with THF:hexane (1:4) yielded 1-(3,5-dimethylphenyl)-1H-imidazole-5-carbonitrile (0.4 g, 2.0 mmol, 2.7% yield) and 1-(3,5-dimethylphenyl)-1H-imidazole-4-carbonitrile (2.0 g, 10.1 mmol, 14% yield).
To a stirred solution of 1-(3,5-dimethylphenyl)-1H-imidazole-4-carbonitrile (1.6 g, 8.1 mmol) in DCM (25 mL), methyl trifluoromethanesulfonate (1.3 g, 8.1 mmol) was added and stirred at room temperature for 4 hours. The precipitate was filtered and washed with DCM yielded 4-cyano-1-(3,5-dimethylphenyl)-3-methyl-1H-imidazol-3-ium trifluoromethanesulfonate (2.4 g, 6.6 mmol, 82% yield).
To a stirred solution of 1-(3,5-dimethylphenyl)-1H-imidazole-5-carbonitrile (0.4 g, 2.0 mmol) in DCM (3 mL), methyl trifluoromethanesulfonate (0.3 g, 2.0 mmol) was added and stirred at room temperature for 4 hours. The precipitate was filtered and washed with DCM yielded 5-cyano-1-(3,5-dimethylphenyl)-3-methyl-1H-imidazol-3-ium trifluoromethanesulfonate (0.5 g, 1.5 mmol, 72.3% yield).
Aniline (2.75 mL, 30.1 mmol) was added into THF (60 mL). Sodium hydride (0.867 g, 36.1 mmol) was added and stirred for 1 hour. 3-Fluoro-2-nitrobenzonitrile (5 g, 30.1 mmol) was added and stirred for about 16 hours at room temperature. Water (2 mL) was added to quench the unreacted sodium hydride. The solvent was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 6.0 g (83% yield) of a red solid was obtained.
2-Nitro-3-(phenylamino)benzonitrile (6 g, 25 mmol) was dissolved in ethanol (200 mL). Sodium dithionite (26 g, 150 mmol) was dissolved in water (200 mL) and added to the ethanol solution. The reaction mixture was heated at 60° C. for 2 hours. The reaction was cooled down to room temperature and filtered off the insoluble inorganic salt. The filtrate was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 3.0 g (57% yield) of a pale yellow oil was obtained.
2-Amino-3-(phenylamino)benzonitrile (3 g, 14.3 mmol) was dissolved in triethyl orthoformate (40 mL, 239 mmol). 12.4 M hydrochloric acid (2 mL) was added and heated at 140° C. for 3 hours. The solvent was then evaporated and the residue was then purified by boiling by heptane:toluene (9:1). 2.5 g (83% yield) of an off-white solid was obtained.
1-Phenyl-1H-benzo[d]imidazole-4-carbonitrile (2.5 g, 11.4 mmol) was dissolved in MeCN. Iodomethane (40 mL, 2M in tert-butyl methyl ether) was added and heated at 70° C. for 3 days. The solid formed was filtered and washed by diethyl ether. The off white solid was further purified by boiling by 1,2-dimethoxyethane:MeCN (19:1). 2.6 g (65% yield) of a white solid was obtained.
Synthesis of Ir(LA43)3
A mixture of LA43 (1.02 g, 2.83 mmol), sodium carbonate (0.100 g, 0.940 mmol) and 2-benzylpyridine iridium (IIII) chloro dimer (0.530 g, 0.470 mmol) in 2-ethoxyethanol (10 mL) was degassed using vacuum/backfill cycles and heated at reflux under nitrogen for 16 hours. The mixture was cooled to room temperature, diluted with water and extracted three times with DCM. The organic extracts were washed with brine, dried with MgSO4, and coated on celite. Purification by column chromatography yielded 71 mg (9% yield) of mer-Ir(LA43)3 and 230 mg (28% yield) of fac-Ir(LA43)3, both as pale yellow solids.
m-Toluidine (3.87 mL, 36.1 mmol) was added into THF (60 mL). Sodium hydride (1.1 g, 45.2 mmol) was added and stirred for 1 hour. 3-Fluoro-2-nitrobenzonitrile (5.0 g, 30.1 mmol) was added and stirred for 16 hours at room temperature. Water (2 mL) was added to quench the unreacted sodium hydride. The solvent was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 6.0 g (79% yield) of a red solid was obtained.
2-Nitro-3-(tolylamino)benzonitrile (6 g, 23.7 mmol) was dissolved in ethanol (200 mL). Sodium dithionite (26 g, 150 mmol) was dissolved in water (200 mL) and added to the ethanol solution. The reaction mixture was heated at 60° C. for 2 hours. The reaction was cooled down to room temperature and filtered off the insoluble inorganic salt. The filtrate was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 3.0 g (47% yield) of a pale yellow oil was obtained.
2-Amino-3-(tolylamino)benzonitrile (3.0 g, 13.4 mmol) was dissolved in triethyl orthoformate (40 mL, 239 mmol), 12.4 M hydrochloric acid (2 mL) was added and heated at 140° C. for 3 hours. The solvent was then evaporated and the residue was then purified by boiling by heptane:toluene (9:1). 2.5 g of (80% yield) an off-white solid was obtained.
1-(m-Toly)-1H-benzo[d]imidazole-4-carbonitrile (2.5 g, 10.7 mmol) was dissolved in MeCN. Iodomethane (40 mL, 2M in tert-butyl methyl ether) was added and heated at 70° C. for 3 days. The solid formed was filtered and washed by diethyl ether. The off white solid was further purified by boiling by 1,2-dimethoxyethane:MeCN (19:1), 2.6 g (67% yield) of a white solid was obtained.
Synthesis of Ir(LA44)3 was prepared from LA44 according to the general iridium complexation procedure as described for Ir(LA43)3 to afford 24% yield of fac-Ir(LA44)3 and 3% yield of mer-Ir(LA44)3 as pale yellow solids.
o-Toluidine (2.75 g, 29 mmol) and 3-fluoro-2-nitrobenzonitrile (4.5 g, 27.1 mmol) was added into THF (20 mL) and N,N-diisopropylethylamine (20 mL) and heated at 85° C. for 2 days. The solvent was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 4.5 g (67% yield) of a red solid was obtained.
2-Nitro-2-(tolylamino)benzonitrile (4.5 g, 18.1 mmol) was dissolved in ethanol (200 mL), sodium dithionite (18.8 g, 108 mmol) was dissolved in water (200 mL) and added to the ethanol solution. The reaction mixture was heated at 60° C. for 2 hours. The reaction was cooled down to room temperature and filtered off the insoluble inorganic salt. The filtrate was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 2.0 g (49% yield) of a pale yellow oil was obtained.
2-Amino-2-(tolylamino)benzonitrile (2 g, 9 mmol) was dissolved in triethyl orthoformate (20 mL, 120 mmol), 12.4 M hydrochloric acid (2 mL) was added and heated at 140° C. for 3 hours. The solvent was then evaporated and the residue was then purified by boiling by heptane:toluene (9:1). 1.7 g (80% yield) of an offwhite solid was obtained.
1-(o-toly)-1H-benzo[d]imidazole-4-carbonitrile (1.7 g, 7.2 mmol) was dissolved in MeCN. Iodomethane (40 ml, 2M in tert-butyl methyl ether) was added and heated at 70° C. for 2 days. The solid formed was filtered and washed by diethyl ether. The off white solid was further purified by boiling by 1,2-dimethoxyethane:MeCN (19:1). 1.8 g (67% yield) of a white solid was obtained.
3,4-Dimethylaniline (4.4 g, 36.1 mmol) was added into THF (60 mL). Sodium hydride (1.1 g, 45.2 mmol) was added and stirred for 1 hour. 3-Fluoro-2-nitrobenzonitrile (5 g, 30.1 mmol) was added and stirred for about 16 hours at room temperature. Water (2 mL) was added to quench the unreacted sodium hydride. The solvent was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 6.5 g (81% yield) of a red solid was obtained.
2-Nitro-3-(3,4-dimethylphenyl)benzonitrile (6.5 g, 24.3 mmol) was dissolved in ethanol (200 mL). Sodium dithionite (26 g, 150 mmol) was dissolved in water (200 mL) and added to the ethanol solution. The reaction mixture was heated at 60° C. for 2 hours. The reaction was cooled down to room temperature and filtered off the insoluble inorganic salt. The filtrate was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 3.0 g (52% yield) of a pale yellow oil was obtained.
2-Amino-3-(3,4-dimethylphenyl)benzonitrile (3.0 g, 12.6 mmol) was dissolved in triethyl orthoformate (40 mL, 239 mmol). 12.4 M hydrochloric acid (2 mL) was added and heated at 140° C. for 3 hours. The solvent was then evaporated and the residue was then purified by boiling by heptane:toluene (9:1). 2.5 g (79% yield) of an off-white solid was obtained.
1-(3,4-Dimethylphenyl)-1H-benzo[d]imidazole-4-carbonitrile (2.5 g, 10.1 mmol) was dissolved in MeCN. Iodomethane (40 mL, 2M in tert-butyl methyl ether) was added and heated at 70° C. for 7 days. The solid formed was filtered and washed by diethyl ether. The off white solid was further purified by boiling by 1,2-dimethoxyethane:MeCN (19:1). 2.6 g (69% yield) of a white solid was obtained.
Synthesis of Ir(LA47)3 was prepared from LA47 according to the general iridium complexation procedure as described for Ir(LA43)3 to afford 0.5% yield of fac-Ir(LA47)3 as a pale yellow solid.
To 3,5-dimethylaniline (3.9 g, 32.2 mmol) in THF (90 mL) was added sodium hydride (95% in mineral oil, 1.23 g, 48.9 mmol) and stirred for 1 hour. 3-Fluoro-2-nitrobenzonitrile (4.3 g, 25.9 mmol) was added and the reaction mixture was heated to reflux for about 16 hours. Reaction mixture cooled to room temperature, then water was added and filtered through silica gel, washed with 5% THF in hexane and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 10% THF in hexane to give orange powder which was recrystallised with 10% 1,2-dimethoxyethane in hexane to give 3-((3,5-dimethylphenyl)amino)-2-nitrobenzonitrile (3.8 g, 55% yield) as an orange powder.
A mixture of 3-((3,5-dimethylphenyl)amino)-2-nitrobenzonitrile (3.8 g, 14.31 mmol) in EtOH (150 mL) and Na2S2O4 (14.9 g, 85 mmol) in water (110 mL) was heated to 80° C. for 2 hours. Reaction mixture was filtered, the filtrate was concentrated and filtered through a Celite/MgSO4 pad and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 10% THF in hexane to give 2-amino-3-((3,5-dimethylphenyl)amino)benzonitrile (2.8 g, 82% yield) as off-white powder.
A mixture of 2-amino-3-((3,5-dimethylphenyl)amino)benzonitrile (2.8 g, 11.81 mmol) in triethyl orthoformate (30 mL) was added concentrated HCl (2.0 mL, 24.0 mmol) and heated to reflux for 2 hours. Reaction mixture cooled to room temperature and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 10-20% THF in hexane to give 1-(3,5-dimethylphenyl)-1H-benzo[d]imidazole-4-carbonitrile (2.5 g, 87% yield) as white powder.
A mixture of 1-(3,5-dimethylphenyl)-1H-benzo[d]imidazole-4-carbonitrile (2.5 g, 10.23 mmol) and methyl trifluoromethanesulfonate (1.8 mL, 16.3 mmol) in DCM (50 mL) was stirred for 18 hours. Solid formed was filtered (4.0 g) and the white powder was recrystallised with 10% 1,2-dimethoxyethane in hexane to give 4-cyano-1-(3,5-dimethylphenyl)-3-methyl-1H-benzo[d]imidazol-3-ium trifluoromethanesulfonate (3.6 g, 86% yield) as white powder.
A mixture of LA49 (0.82 g, 2.0 mmol), sodium carbonate (0.21 g, 2.0 mmol), silver carbonate (0.55 g, 2.0 mmol), and iridium (III) chloride hydrate (0.22 g, 0.6 mmol) in 2-ethoxyethanol (15. mL) was degassed using vacuum/backfill cycles and heated at reflux for 16 hours. This reaction was combined with another reaction run at 50%-scale and then diluted with water and extracted three times with DCM. The combined organic layers were dried, coated on celite, and purified by column chromatography to yield 29 mg (3%) of mer-Ir(LA49)3 as a pale yellow solid.
3,4,5-Trimethylaniline (4.9 g, 36.1 mmol) was added into THF (60 mL). Sodium hydride (1.1 g, 45.2 mmol) was added and stirred for 1 hour. 3-Fluoro-2-nitrobenzonitrile (5.0 g, 30.1 mmol) was added and stirred for about 16 hours at room temperature. Water (2 mL) was added to quench the unreacted sodium hydride. The reaction mixture was concentrated in vacuo and the residue was purified by flash column chromatography using THF:hexane (1:4, v/v) as the eluent to give 2-nitro-3-((3,4,5-trimethylphenyl)amino)benzonitrile (7.0 g, 82% yield) as red solid.
A mixture of 2-nitro-3-((3,4,5-trimethylphenyl)amino)benzonitrile (6.56 g, 23.4 mmol) in EtOH (275 mL), THF (25 mL) and Na2S2O4 (20.3 g, 117 mmol) in water (200 mL) was heated to 80° C. for 2 hours. Reaction mixture was filtered. The filtrate was concentrated and filtered through a Celite/MgSO4 pad and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 5-15% THF in hexane to give white powder (3.1 g) which was recrystallised with 10% 1,2-dimethoxyethane in heptane to give 2-amino-3-((3,4,5-trimethylphenyl)amino)benzonitrile (2.6 g, 44% yield) as white powder.
A mixture of 2-amino-3-((3,4,5-trimethylphenyl)amino)benzonitrile (2.6 g, 10.3 mmol) in triethyl orthoformate (30 mL) was added concentrated HCl (1.8 mL, 21.6 mmol) and heated to reflux for 2 hours. Reaction mixture cooled to room temperature and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 5-10% THF in hexane to give 1-(3,4-dimethylphenyl)-1H-benzo[d]imidazole-6-carbonitrile (2.6 g, 96% yield) as white powder.
A mixture of 1-(3,4-dimethylphenyl)-1H-benzo[d]imidazole-6-carbonitrile (2.6 g, 10.0 mmol) and methyl trifluoromethanesulfonate (1.8 mL, 15.91 mmol) in DCM (100 mL) was stirred for 18 h. Reaction mixture was concentrated to 40-50 mL and added diethyl ether (30 mL). The solid formed was filtered and the white powder was recrystallised with 10% 1,2-dimethoxyethane in MeCN to give 4-cyano-3-methyl-1-(3,4,5-trimethylphenyl)-1H-benzo[d]imidazol-3-ium trifluoromethanesulfonate (2.3 g, 51% yield) as white powder.
Biphenylamine (4.6 g, 27 mmol) and 3-fluoro-2-nitrobenzonitrile (5.0 g, 30.1 mmol) was added into THF (20 mL) and N,N-diisopropylethylamine (20 mL) and heated at 85° C. for 2 days. The solvent was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 7.0 g (82% yield) of a red solid was obtained.
3-([1,1′-Biphenyl]-3-ylamino)-2-nitrobenzonitrile (7.0 g, 22 mmol) was dissolved in ethanol (200 mL). Sodium dithionite (26 g, 150 mmol) was dissolved in water (200 mL) and added to the ethanol solution. The reaction mixture was heated at 60° C. for 2 hours. The reaction was cooled down to room temperature and filtered off the insoluble inorganic salt. The filtrate was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 3.5 g (56% yield) of a pale yellow oil was obtained.
3-([1,1′-Biphenyl]-3-ylamino)-2-aminobenzonitrile (3.5 g, 12.2 mmol) was dissolved in triethyl orthoformate (40 mL, 239 mmol), 12.4 M hydrochloric acid (2 mL) was added and heated at 140° C. for 3 hours. The solvent was then evaporated and the residue was then purified by boiling by heptane:toluene (9:1). 3.0 g (82% yield) of an off-white solid was obtained.
1-([1,1′-Biphenyl]-3-yl)-1H-benzo[d]imidazole-4-carbonitrile (3.0 g, 10.1 mmol) was dissolved in MeCN. Iodomethane (40 mL, 2M in tert-butyl methyl ether) was added and heated at 70° C. for 7 days. The solid formed was filtered and washed by diethyl ether. The off white solid was further purified by boiling by 1,2-dimethoxyethane:MeCN (19:1). 2.2 g of a white solid was obtained.
3-Dibenzofuranamine (4.2 g, 23 mmol) and 3-fluoro-2-nitrobenzonitrile (5.0 g, 30.1 mmol) were added into THF (20 mL) and N,N-diisopropylethylamine (20 mL) and heated at 85° C. for 2 days. The solvent was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 6.0 g (79% yield) of a red solid was obtained.
2-Nitro-3-(dibenzo[b,d]furan-3-ylamino)benzonitrile (6.0 g, 18.2 mmol) was dissolved in ethanol (200 mL). Sodium dithionite (26 g, 150 mmol) was dissolved in water (200 mL) and added to the ethanol solution. The reaction mixture was heated at 60° C. for 2 hours. The reaction was cooled down to room temperature and filtered off the insoluble inorganic salt. The filtrate was then evaporated and the residue was then purified by column chromatography using THF:hexane (1:4, v/v) as the eluent. 3.0 g (55% yield) of a pale yellow oil was obtained.
2-Amino-3-(dibenzo[b,d]furan-3-ylamino)benzonitrile (3.0 g, 10 mmol) was dissolved in triethyl orthoformate (40 mL, 239 mmol). 12.4 M hydrochloric acid (2 mL) was added and heated at 140° C. for 3 h. The solvent was then evaporated and the residue was then purified by boiling by heptane:toluene (9:1). 2.5 g (81% yield) of an off-white solid was obtained.
1-(Dibenzo[b,d]furan-3-ylamino)-1H-benzo[d]imidazole-4-carbonitrile (2.5 g, 8.1 mmol) was dissolved in MeCN. Iodomethane (40 mL, 2M in tert-butyl methyl ether) was added and heated at 70° C. for 7 days. The solid formed was filtered and washed by diethyl ether. The off white solid was further purified by boiling by 1,2-dimethoxyethane:MeCN (19:1). 2.6 g (70% yield) of a white solid was obtained.
Synthesis of Ir(LA59)3 was prepared from LA59 according to the general iridium complexation procedure as described for Ir(LA43)3 to afford 17% yield of mer-Ir(LA59)3 as a pale yellow solid.
Sodium tert-butoxide (2.5 g, 26.4 mmol) and THF (50 mL) were mixed at 0° C. 1M DIBAL (24 mL, 24.0 mmol) was added at 0° C. The mixture was stirred for 1 h at 0° C. Methyl 1-phenyl-1H-benzo[d]imidazole-6-carboxylate (3.0 g. 12.0 mmol) in THF (50 mL) was added at 0° C. The resultant mixture was stirred for 4 hours at 0° C. The reaction mixture was quenched by the addition of water and extracted with DCM. The extracts were dried over MgSO4 and a silica pad and the solvent was removed in vacuo. The residue was purified by flash chromatography using 5% MeOH in DCM to afford (1-phenyl-1H-benzo[d]imidazol-6-yl)methanol (2.4 g, 88% yield) as a brown oil.
45% 2-Iodoxybenzoic acid (9.0 g, 14.4 mmol) and DMSO (20 mL) were mixed and stirred for 20 min at room temperature. (1-phenyl-1H-benzo[d]imidazol-6-yl)methanol (2.4 g, 10.6 mmol) was added and stirred for 4 hours at room temperature. The mixture was quenched by MeOH. The reaction mixture was filtered through a silica pad and washed with 10% MeOH in DCM. The solvent was removed in vacuo. The residue was purified by flash chromatography using 2% MeOH in DCM. The product was purified by re-crystallization in 40% DCE in heptane to afford 1-phenyl-1H-benzo[d]imidazole-6-carbaldehyde (2.0 g, 85% yield) as a white solid.
1-Phenyl-1H-benzo[d]imidazole-6-carbaldehyde (2.0 g, 9.0 mmol), THF (75 mL), 30% NH3(aq) (11.7 mL, 90.0 mmol) and iodine (6.9 g, 27.0 mmol) were mixed at and stirred for 18 hours at room temperature. The reaction mixture was quenched by the addition of saturated Na2S2O3 and extracted with DCM. The extracts were dried over MgSO4 and a silica pad and washed with 2% MeOH in DCM. The solvent was removed in vacuo. The residue was purified by flash chromatography using 2% MeOH in DCM. The product was purified by re-crystallization in 30% 1,4-dioxane in heptane to afford 1-phenyl-1H-benzo[d]imidazole-6-carbonitrile (1.5 g, 76% yield) as a white solid.
1-Phenyl-1H-benzo[d]imidazole-6-carbonitrile (1.5 g, 6.8 mmol), toluene (10 mL) and iodomethane (10 mL) were mixed. The resultant mixture was refluxed for 24 hours. After cooling, the precipitate was filtered and further purified by re-crystallization in 10% MeCN in 1,2-dimethoxyethane to afford 6-cyano-3-methyl-1-phenyl-1H-benzo[d]imidazol-3-ium iodide (1.9 g, 77% yield) as a white solid.
Synthesis of Ir(LA85)3 was prepared from LA85 according to the general iridium complexation procedure as described for Ir(LA43)3 to afford 17% yield of fac-Ir(LA85)3 and 9% yield of mer-Ir(LA85)3 as pale yellow solids.
To m-toluidine (4.5 g, 42.0 mmol) in THF (100 mL) was added sodium hydride (95% in mineral oil, 1.6 g, 62.9 mmol) and stirred for 1 hour. 3-Fluoro-4-nitrobenzonitrile (5.8 g, 35.0 mmol) was added and the reaction mixture was heated to reflux overnight. The reaction mixture cooled to room temperature, water was added and filtered through silica gel, washed with 5% THF in hexane and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 5-10% THF in hexane to give 4-nitro-3-(m-tolylamino)benzonitrile (5.5 g, 61% yield) as an orange powder.
A mixture of 4-nitro-3-(m-tolylamino)benzonitrile (5.2 g, 20.7 mmol) in EtOH (200 mL) and Na2S2O4 (14.4 g, 83.0 mmol) in water (100 mL) was heated to 80° C. for 2 hours. Reaction mixture was filtered, the filtrate was concentrated and filtered through a Celite/MgSO4 pad and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 5-15% THF in hexane to give 4-amino-3-(m-tolylamino)benzonitrile (4.3 g, 93% yield) as yellow oil.
A mixture of 4-amino-3-(m-tolylamino)benzonitrile (4.6 g, 20.6 mmol) in triethyl orthoformate (75 mL) was added concentrated HCl (1.25 mL, 41.1 mmol) and heated to reflux for 2 hours. Reaction mixture was cooled to room temperature and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 5-10% THF in hexane to give 1-(m-tolyl)-1H-benzo[d]imidazole-6-carbonitrile (4.3 g, 900/% yield) as white powder.
To 1-(m-tolyl)-1H-benzo[d]imidazole-6-carbonitrile (3.6 g, 15.5 mmol) in MeCN (35 mL) was added iodomethane (2.0 M in tert-butylmethylether, 38.8 mL, 78 mmol) and heated to reflux for 15 hours. The white solid was filtered and recrystallised with 10% 1,2-dimethoxyethane in MeCN to give 6-cyano-3-methyl-1-(m-tolyl)-1H-benzo[d]imidazol-3-ium iodide (4.7 g, 81% yield) as white powder.
Synthesis of Ir(LA86)3 was prepared from LA86 according to the general iridium complexation procedure as described for Ir(LA43)3 to afford 3% yield of fac-Ir(LA86)3 and 4% yield of mer-Ir(LA86)3 as pale yellow solids.
To 3,4-dimethylaniline (4.4 g, 35.9 mmol) in THF (100 mL) was added sodium hydride (95% in mineral oil, 1.34 g, 55.8 mmol) and stirred for 1 hour. 3-Fluoro-4-nitrobenzonitrile (5.0 g, 30.1 mmol) was added and the reaction mixture was heated to reflux for 8 hours. Reaction mixture was cooled to room temperature, water was added and filtered through silica gel, washed with 5% THF in hexane and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 5-10% THF in hexane to give 3-((3,4-dimethylphenyl)amino)-4-nitrobenzonitrile (3.4 g, 36% yield) as an orange powder.
A mixture of 3-((3,4-dimethylphenyl)amino)-4-nitrobenzonitrile (2.89 g, 10.7 mmol) in EtOH (100 mL) and Na2S2O4 (7.5 g, 43.1 mmol) in water (75 mL) was heated to 80° C. for 2 hours. Reaction mixture was filtered, the filtrate was concentrated and filtered through a Celite/MgSO4 pad and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 5-15% THF in hexane to give 4-amino-3-((3,4-dimethylphenyl)amino)benzonitrile (2.3 g, 91% yield) as yellow oil.
A mixture of 4-amino-3-((3,4-dimethylphenyl)amino)benzonitrile (2.3 g, 9.5 mmol) in triethyl orthoformate (35 mL) was added concentrated HCl (0.6 mL, 19.0 mmol) and heated to reflux for 2 hours. Reaction mixture was cooled to room temperature and concentrated in vacuo. The crude mixture was purified by flash column chromatography with 5-10% THF in hexane to give 1-(3,4-dimethylphenyl)-1H-benzo[d]imidazole-6-carbonitrile (2.3 g, 99% yield) as white powder.
To 1-(3,4-dimethylphenyl)-1H-benzo[d]imidazole-6-carbonitrile (2.0 g, 8.2 mmol) in MeCN (10 mL) was added iodomethane (2.0 M in tert-butylmethylether, 21 mL, 42 mmol) and heated to reflux for 15 hours. The white solid was filtered and recrystallised with 10% 1,2-dimethoxyethane in MeCN to give 6-cyano-1-(3,4-dimethylphenyl)-3-methyl-1H-benzo[d]imidazol-3-ium iodide (2.5 g, 78% yield) as white powder.
Synthesis of Ir(LA89)3 was prepared from LA89 according to the general iridium complexation procedure as described for Ir(LA43)3 to afford 3% yield of fac-Ir(LA89)3 and 7% yield of mer-Ir(LA89)3 as pale yellow solids.
2-Fluoro-3-nitrobenzonitrile (3.8 g, 23.0 mmol), THF (70 mL), aniline (2.7 mL, 30.0 mmol) and N,N-diisopropylethylamine (17.4 mL, 100.0 mmol) were mixed at room temperature. The resultant mixture was refluxed for 7 hours. The reaction mixture was filtered through a silica pad and MgSO4 and washed with 80% THF in hexane. The solvent was removed in vacuo. The product was purified by re-crystallization in 5% THF in hexane to afford 3-nitro-2-(phenylamino)benzonitrile (5.2 g, 77% yield) as an orange solid.
3-Nitro-2-(phenylamino)benzonitrile (4.8 g, 20.0 mmol), EtOH (150 mL) and Na2S2O4 (13.9 g, 80.0 mmol in 150 mL H2O) were mixed at room temperature. The resultant mixture was refluxed for 1 hours. The solvent was removed in vacuo. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. The product was purified by re-crystallization in 20% THF in heptane to afford 3-amino-2-(phenylamino)benzonitrile (2.4 g, 57% yield) as a white solid.
3-Amino-2-(phenylamino)benzonitrile (0.9 g, 4.5 mmol), triethyl orthoformate (50 mL) and 12.4 M hydrochloric acid (0.7 mL, 9.0 mmol) were mixed. The resultant mixture was refluxed for 3 hours. After cooling, the solvent was removed in vacuo. The residue was purified by flash chromatography using 2% MeOH in DCM to afford 1-phenyl-1H-benzo[d]imidazole-7-carbonitrile (0.9 g, 89% yield) as a white solid.
1-Phenyl-1H-benzo[d]imidazole-7-carbonitrile (098 g, 4.0 mmol), DCM (20 mL) and methyl trifluoromethanesulfonate (0.8 mL, 7.0 mmol) were mixed and stirred for 15 hours at room temperature. The resultant mixture was diluted by Et2O. The precipitate was filtered and dried to afford 7-cyano-3-methyl-1-phenyl-1H-benzo[d]imidazol-3-ium trifluoromethanesulfonate (1.4 g, 91% yield) as a white solid.
Synthesis of Ir(LA106)3 was prepared from LA106 according to the general iridium complexation procedure as described for Ir(LA43)3 to afford 14% yield of fac-Ir(LA106)3 and 6% yield of mer-Ir(LA106)3 as pale yellow solids.
2-Fluoro-3-nitrobenzonitrile (4.2 g, 25.0 mmol), THF (50 mL), m-toluidine (4.0 mL, 37.5 mmol) and N,N-diisopropylethylamine (13.0 mL, 75.0 mmol) were mixed at room temperature. The resultant mixture was refluxed for 7 hour. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. The product was purified by re-crystallization in 10% THF in hexane to afford 3-nitro-2-(m-tolylamino)benzonitrile (6.0 g, 94% yield) as an orange solid.
3-Nitro-2-(m-tolylamino)benzonitrile (5.9 g, 23.5 mmol), EtOH (150 mL) and Na2S2O4 (16.4 g, 94.0 mmol in 150 mL H2O) were mixed at room temperature. The resultant mixture was refluxed for 1 hour. The solvent was removed in vacuo. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. Then, the solid was dissolved in triethyl orthoformate (50 mL). 12.4 M hydrochloric acid (3.8 mL, 47.0 mmol) was added. The resultant mixture was refluxed for 3 hours. The resultant mixture was diluted by 20% Et2O in hexane. The precipitate was filtered to afford 1-(m-tolyl)-1H-benzo[d]imidazole-5,6-dicarbonitrile (4.6 g, 83% yield over 2 steps) as a white solid.
1-(m-Tolyl)-1H-benzo[d]imidazole-5,6-dicarbonitrile (4.6 g, 20.0 mmol), DCM (300 mL) and methyl trifluoromethanesulfonate (2.5 mL, 22.8 mmol) were mixed and stirred for 43 hours at room temperature. The resultant mixture was diluted by Et2O and filtered. The product was further purified by re-crystallization in 60% 1,2-dimethoxyethane in heptane and then 10% MeCN in ether to afford 7-cyano-3-methyl-1-(m-tolyl)-1H-benzo[d]imidazol-3-ium trifluoromethanesulfonate (6.6 g, 84% yield) as a pale yellow solid.
2-Fluoro-3-nitrobenzonitrile (4.2 g, 25.0 mmol), THF (50 mL), 3,5-dimethylaniline (4.0 mL, 32.0 mmol) and N,N-diisopropylethylamine (17.3 mL, 100.0 mmol) were mixed at room temperature. The resultant mixture was refluxed for 9 hours. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. The product was purified by re-crystallization in 10% THF in hexane to afford 2-((3,5-dimethylphenyl)amino)-3-nitrobenzonitrile (6.4 g, 96% yield) as an orange solid.
2-((3,5-Dimethylphenyl)amino)-3-nitrobenzonitrile (6.4 g, 24.0 mmol), EtOH (150 mL) and Na2S2O4(16.7 g, 96.0 mmol in 150 mL H2O) were mixed at room temperature. The resultant mixture was refluxed for 2 hours. The solvent was removed in vacuo. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. Then, the solid was dissolved in orthoformate (80 mL). 12.4 M hydrochloric acid (3.9 mL, 48.0 mmol) was added. The resultant mixture was refluxed for 3 hours. The solvent was removed in vacuo. The residue was purified by flash chromatography using 65% THF in hexane. The product was purified by re-crystallization in 10% THF in hexane to afford 1-(3,5-dimethylphenyl)-1H-benzo[d]imidazole-7-carbonitrile (4.2 g, 71% yield over 2 steps) as a white solid.
1-(3,5-Dimethylphenyl)-1H-benzo[d]imidazole-7-carbonitrile (4.2 g, 17.0 mmol), DCM (50 mL) and methyl trifluoromethanesulfonate (2.0 mL, 18.3 mmol) were mixed and stirred for 24 hours at room temperature. The resultant mixture was diluted by Et2O and filtered. The product was further purified by re-crystallization in 30% 1,2-dimethoxyethane in heptane and then 6% MeCN in ether to afford 7-cyano-1-(3,5-dimethylphenyl)-3-methyl-1H-benzo[d]imidazol-3-ium trifluoromethanesulfonate (6.6 g, 94% yield) as a white solid.
4-Bromo-5-nitrophthalonitrile (5.0 g, 20.0 mmol), THF (70 mL), aniline (2.7 mL, 30.0 mmol) and N,N-diisopropylethylamine (17.4 mL, 100.0 mmol) were mixed at room temperature. The resultant mixture was refluxed for 2 hours. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. The product was purified by re-crystallization in 5% THF in hexane to afford 4-nitro-5-(phenylamino)phthalonitrile (5.2 g, 98% yield) as an orange solid.
4-Nitro-5-(phenylamino)phthalonitrile (4.5 g, 17.0 mmol), EtOH (150 mL) and Na2S2O4 (11.8 g, 68.0 mmol in 150 mL H2O) were mixed at room temperature. The resultant mixture was refluxed for 1 hour. The solvent was removed in vacuo. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. The product was purified by re-crystallization in 20% THF in hexane to afford 4-amino-5-(phenylamino)phthalonitrile (3.3 g, 83% yield) as a white solid.
4-Amino-5-(phenylamino)phthalonitrile (3.3 g, 14.0 mmol), triethyl orthoformate (80 mL) and 12.4 M hydrochloric acid (2.3 mL, 28.0 mmol) were mixed. The resultant mixture was refluxed for 3 hours. The resultant mixture was diluted by 50% Et2O in hexane. The precipitate was filtered and dried to afford 1-phenyl-1H-benzo[d]imidazole-5,6-dicarbonitrile (2.6 g, 77% yield) as a white solid.
1-Phenyl-1H-benzo[d]imidazole-5,6-dicarbonitrile (3.9 g, 16.0 mmol), DCM (150 mL) and methyl trifluoromethanesulfonate (3.4 mL, 31.0 mmol) were mixed and stirred for 25 h at room temperature. The resultant mixture was diluted by Et2O. The precipitate was filtered and further purified by re-crystallization in 20% MeCN in 1,2-dimethoxyethane to afford 5,6-dicyano-3-methyl-1-phenyl-1H-benzo[d]imidazol-3-ium trifluoromethanesulfonate (4.9 g, 75% yield) as a white solid.
4-Bromo-5-nitrophthalonitrile (5.0 g, 20.0 mmol), THF (50 mL), m-toluidine (3.2 mL, 30.0 mmol) and N,N-diisopropylethylamine (15.0 mL, 86.0 mmol) were mixed at room temperature. The resultant mixture was refluxed for 15 hours. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. The product was purified by re-crystallization in 10% THF in hexane to afford 4-nitro-5-(m-tolylamino)phthalonitrile (5.5 g, 99% yield) as an orange solid.
4-Nitro-5-(m-tolylamino)phthalonitrile (5.5 g, 20.0 mmol), EtOH (150 mL) and Na2S2O4 (13.9 g, 80.0 mmol in 150 mL H2O) were mixed at room temperature. The resultant mixture was refluxed for 2 hours. The solvent was removed in vacuo. The reaction mixture was filtered through a silica pad and MgSO4 and washed with THF. The solvent was removed in vacuo. Then, the solid was dissolved in triethyl orthoformate (90 mL). 12.4 M hydrochloric acid (3.2 mL, 40.0 mmol) was added. The resultant mixture was refluxed for 3 hours. The resultant mixture was diluted by 20% Et2O in hexane. The precipitate was filtered and dried to afford 1-(m-tolyl)-1H-benzo[d]imidazole-5,6-dicarbonitrile (3.3 g, 65% yield over 2 steps) as a white solid.
1-(m-Tolyl)-1H-benzo[d]imidazole-5,6-dicarbonitrile (3.4 g, 13.0 mmol), DCM (300 mL) and methyl trifluoromethanesulfonate (2.0 mL, 18.2 mmol) were mixed and stirred for 15 hours at room temperature. The resultant mixture was diluted by Et2O. The precipitate was filtered and further purified by re-crystallization in 25% MeCN in 1,2-dimethoxyethane to afford 5,6-dicyano-3-methyl-1-(m-tolyl)-1H-benzo[d]imidazol-3-ium trifluoromethanesulfonate (4.6 g, 83% yield) as a white solid.
3-Amino-4-(phenylamino)benzonitrile (6.0 g, 20.0 mmol), triethyl orthoformate (50 mL) and 12.4 M hydrochloric acid (3.2 mL, 40.0 mmol) were mixed. The resultant mixture was refluxed for 3 hours. After cooling, the solvent was removed in vacuo. The residue was purified by flash chromatography using 5% MeOH in DCM. The product was further purified by re-crystallization in 60% Et2O in hexane to afford 1-phenyl-1H-benzo[d]imidazole-5-carbonitrile (3.8 g, 88% yield) as a white solid.
1-Phenyl-1H-benzo[d]imidazole-5-carbonitrile (3.7 g, 17.0 mmol), toluene (50 mL) and iodomethane (25 mL) were mixed. The resultant mixture was refluxed for 40 hours. After cooling, the precipitate was filtered and further purified by re-crystallization in 10% MeCN in 1,2-dimethoxyethane to afford 5-cyano-3-methyl-1-phenyl-1H-benzo[d]imidazol-3-ium iodide (5.8 g, 95% yield) as a white solid.
Synthesis of Comparative Compound 1 was prepared according to the general iridium complexation procedure as described for Ir(LA43)3 to afford 21% yield of Comparative Compound 1 as a white solid.
The photophysical and electrochemical properties (oxidation potential, Eox and reduction potential, Ered, determined by solution cyclic voltammetry using Fc/Fc+ as the reference) of various examples of the inventive compounds and comparative compounds are summarized in Table 1 below. For Eox and Ered, (R) means the wave is reversible and (IR) means the wave is irreversible.
The structure of the comparative compounds are as follows:
The data shows that having an electron withdrawing group such as CN at certain positions of the carbene can dramatically improve the photophysical and electromchemically properties of the compounds. For example, fac-Ir(LA44)3 has a CN group at the Rc1 position. The Emission λmax is 454 nm, PLQY is 92%, excited state lifetime is 1.86 μs, Eox, is 0.54 V (R) and Ered is −2.45V (R). On the other hand, for Comparative Compound 1 having a CN group at the Rc2 position Emission λmax is 410 nm, PLQY is 51%, excited state lifetime is 27 μs, Eox is 0.64 V (R) and Ered is −2.59 V (IR). For the unsubstituted compound Comparative Compound 2, the Emission λmax is 378 nm, PLQY is 48%, excited state lifetime is 3.18 μs, Eox is 0.50 V (R) and Ered is undetected. The dramatic difference in the emission, PLQY and excited state lifetime demonstrate that the position of the electron withdrawing group is important in obtaining high-efficiency blue phosphorescent emitters. The data has shown that for the benzimidazole carbene system (Formular II), the electron withdrawing groups at Rc1, Rc3 and Rc4 positions exhibited unexpected substantial difference compared to having an electron withdrawing group at Rc2 position. Namely, having electron withdrawing groups at Rc1, Rc3 and Rc4 positions result in more favorable effect on the photophysical and electrochemical properties compared to the Rc2 position.
All device examples were fabricated by high vacuum (<10−7 Torr) thermal evaporation. The anode electrode was ˜800 Å of indium tin oxide (ITO). The cathode consisted of 5 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 H2O and O2) and a moisture getter was incorporated inside the package. Some of the compounds used in fabricating the device examples are shown below.
The organic stack of Device Example 1-6 consists of 100 Å of LG101 (from LG Chem, Korea) as the hole injection layer (HIL), 250 Å of Compound A as the hole transporting layer (HTL), 50 Å of Compound B or Compound E as the electron blocking layer (EBL) when EBL was used, 300 Å of host doped with 10% of Compound fac-Ir(LA44)3 as the emissive layer (EML), 50 Å of Compound D or F as the hole blocking layer (HBL), and 300 Å of Liq (Li(8 hydroxyquinolate) doped with 35% of LG201 (from LG Chem, Korea) as the electron transporting layer (ETL). The data is summarized in Table 2.
As shown in Table 2, blue emitting phosphorescent OLED can be achieved with CIE of <0.15, <0.17 with external quantum efficiency of >4%. Guassian emission profiles are also obtained instead of vibronic emission profiles commonly observed in blue phosphorescent OLED, suggesting increased MLCT and π backbonding character between the metal center and the imidazole carbene. These features indicate a strong bond between the metal center and the imidazole carbene cyclometallating carbon. Additionally, UV photoisomerization under nitrogen, typically an effective way of converting mer to fac isomers in Ir cyclometallated complexes, did not cause isomerization of mer-Ir(LA49)3. This result suggests that the metal-carbon bond is indeed strong.
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.
This application claims priority to U.S. Provisional Application Ser. No. 62/107,446, filed Jan. 25, 2015, the entire contents of which is incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 62107446 | Jan 2015 | US |
