Patent Grant
8957217
The invention relates to a class of phosphorescent materials, their preparation methods and organic light emitting diodes (OLEDs) using these materials.
The first organic light-emitting diode (OLED) was disclosed by Tang et. al. (U.S. Pat. No. 4,356,429) and Tang et. al. (Appl. Phys. Lett. 1987, 51, 12, 913). Subsequently, device architecture and emissive materials for OLED applications have been intensively studied. OLEDs allow devices that are (1) ultra-thin; (2) self-emissive; (3) use low operating voltage with high efficiency; and (4) display high contrast and resolution.
Phosphorescent materials are the primary direction of emissive material development, because these OLED devices generate 25% singlet and 75% triplet excitons. Devices fabricated from phosphorescent materials generally display efficiencies that are higher than devices fabricated from fluorescent materials. Platinum complexes are a class of emissive materials that offer high emission quantum efficiency and good thermal stability. High performance OLEDs have been formed using platinum(II) complexes. (Yan et al., Appl. Phys. Lett. 2007, 91(6) 063508; Che et al., Chemistry—A European Journal 2010, 16(1), 233)
Producing blue-emitting phosphorescent materials has proven to be challenging. However, high performance and long lifetime blue-emitting OLEDs have not been fabricated from platinum(II) complexes. To tune the emission color of platinum(II) complexes, the appropriate conjugation length of the ligand is essential. Neutral blue-emitting Pt(II) complex were prepared by coordinating two bidentate ligands to a Pt(II) center, resulting in the first blue-emitting Pt(II) complexes. (Brooks et al., Inorg. Chem. 2002, 41, 3055; and Unger et al., Angew. Chem. Int. Ed. 2010, 49, 10214) However, binding forces between these bidentate ligands and the platinum(II) center in these complexes are weaker than the binding forces of complexes containing one tetradentate ligand bound to a Pt(II). The devices that form these bis-bidentate ligand Pt(II) complexes display lifetimes and stabilities that are inferior to device tetradentate Pt(II) complexes. Ligand systems having more than two aryl groups, coupled by a non-conjugated unit, do not provide emission maxima less than 480 nm. (U.S. Pat. No. 7,026,480, U.S. Pat. No. 6,653,654). Blue-emitting materials have not been made from this type of tridentate or tetradentate ligands. Efforts directed to tetradentate blue-emitting Pt(II) materials where conjugation groups connect aryl groups of the ligands, have failed to generate complexes with emission maxima less than 480 nm. (U.S. Pat. No. 7,361,415, U.S. Pat. No. 7,691,495 and U.S. Published Patent Application 2007/0103060 A1)
N-heterocyclic carbenes (NHC) are strong σ-donors but poor π-acceptors. Using cyclometalated Pt(II) complexes, Meyer et al., Organometallics, 2011, 30 (11), 2980 discloses Pt(II) complexes with shortened ligand π-conjugations, but does not report of the emission spectra.
Embodiments of the invention are directed to blue phosphorescent platinum(II) complexes of dianionic tetradentate bis-(NHC carbene) ligand of structure II:
wherein R1-R8 are, independently, hydrogen, fluoro, chloro, bromo, iodo, hydroxyl, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, acyl, alkoxy, acyloxy, amino, nitro, acylamino, aralkyl, cyano, carboxyl, thio, styryl, aminocarbonyl, carbamoyl, aryloxycarbonyl, phenoxycarbonyl, or alkoxycarbonyl, and X is, independently, oxygen, nitrogen, sulphur, phosphorus, or selenium. Other embodiments of the invention are directed to the preparation of the tetradentate bis-(NHC carbene) ligands where at least one of R1-R8 are not hydrogen, and OLEDs comprise Pt(II) complexes of tetradentate bis-(NHC carbene) ligands.
Embodiments of the invention are directed to tetradentate ligands comprising a bis-(NHC carbenes) alkylene, as shown in the bis-anion-bis-carbene form in structure I:
wherein R1-R8 are, independently, hydrogen, fluoro, chloro, bromo, iodo, hydroxyl, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, acyl, alkoxy, acyloxy, amino, nitro, acylamino, aralkyl, cyano, carboxyl, thio, styryl, aminocarbonyl, carbamoyl, aryloxycarbonyl, phenoxycarbonyl, or alkoxycarbonyl; and wherein at least one of R1-R8 is not hydrogen; and X is O, NR9, S, PR9, or Se, where R9 is H or alky. In an embodiment of the invention, R6 is not hydrogen. In an embodiment of the invention, R8 is not hydrogen. Embodiments of the invention are directed to stable blue-emitting platinum(II) complexes prepared from ligands comprising bis-(NHC carbenes) where the tetradentate ligand I's electron donor substituents, X, are in anions in a Pt complex of structure II:
wherein R1-R7 are, independently, hydrogen, fluoro, chloro, bromo, iodo, hydroxyl, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, acyl, alkoxy, acyloxy, amino, nitro, acylamino, aralkyl, cyano, carboxyl, thio, styryl, aminocarbonyl, carbamoyl, aryloxycarbonyl, phenoxycarbonyl, or alkoxycarbonyl; wherein at least one of R1-R8 is not hydrogen; and X is O, NR9, S, PR9, or Se, where R9 is H or alky. In an embodiment of the invention, R6 is not hydrogen. In an embodiment of the invention, R8 is not hydrogen
In an embodiment of the invention, the tetradentate ligand precursor is in the protonated form:
wherein R1-R7 are, independently, hydrogen, fluoro, chloro, bromo, iodo, hydroxyl, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, acyl, alkoxy, acyloxy, amino, nitro, acylamino, aralkyl, cyano, carboxyl, thio, styryl, aminocarbonyl, carbamoyl, aryloxycarbonyl, phenoxycarbonyl, or alkoxycarbonyl; wherein at least one of R1-R8 is not hydrogen; X is O, NR9, S, PR9, or Se, where R9 is H or alky; and A− is chloride, bromide, iodide, tosylate, brosylate, triflate, or other anion of low nucleophilicity. In an embodiment of the invention, R6 is not hydrogen. In an embodiment of the invention, R8 is not hydrogen.
Tetradentate ligand precursors III can be prepared by a series of reactions depicted in
Exemplary tetradentate bis-(NHC carbenes) alkylene ligand Pt(II) complexes, according to an embodiment of the invention, are shown in
In an embodiment of the invention, the tetra-protonated bis-(NHC carbenes) alkylene ligand precursor is combined with a Pt(II) salt to form a tetradentate bis-(NHC carbenes) alkylene ligand Pt(II) complex, as illustrated in
According to an embodiment of the invention, tetradentate bis-(NHC carbenes) alkylene ligand Pt(II) complexes are dispersed and immobilized in an inert polymer matrix, for example, but not limited to, poly(methyl methacrylate) (PMMA), to form a highly emissive film in the blue spectral region at a complex to polymer weight ratio of 1% or more. Absolute emission quantum yields for these films are around 30%, as measured with an integrate sphere method at room temperature. Emission maxima of the films can be blue-shifted by up to 10 nm from that for the bis-(NHC carbenes) alkylene ligand Pt(II) complexes in solution, suggesting a solid-solution state in the polymer dispersions. The films exhibit emission with chromaticity, as indicated by Commission Internationale de L'Eclairage coordinates, of CIEx,y<0.2 and CIEx+y<0.3. For example, complex 4, shown in
All patents and publications referred to or cited herein are incorporated by reference in their entirety, including all figures and tables, to the extent they are not inconsistent with the explicit teachings of this specification.
Following are examples that illustrate procedures for practicing the invention. These examples should not be construed as limiting. All percentages are by weight and all solvent mixture proportions are by volume unless otherwise noted.
All starting materials were used as received from commercial sources. The solvents used for photophysical measurements were of HPLC grade. Elemental analyses were performed by the Institute of Chemistry at the Chinese Academy of Sciences, Beijing. Fast atom bombardment (FAB) mass spectra were obtained on a Finnigan Mat 95 mass spectrometer. 1H (300 MHz or 400 MHz) NMR spectra were recorded on DPX300 and Avance400 Bruker FT-NMR spectrometers. UV-Vis spectra were recorded on a Perkin-Elmer Lambda 19 UV/vis spectrophotometer. Steady-state emission and excitation spectra at 298 K and Photoluminescence of films on quartz substrate were obtained on a Spex 1681 Fluorolog-2 Model F111 spectrophotometer equipped with a Hamamatsu R928 PMT detector. All solutions for photophysical measurements, except stated otherwise, were degassed in a high-vacuum line with at least four freeze-pump-thaw cycles. Emission lifetimes were measured with a Quanta-Ray Q-switch DCR-3 Nd:YAG pulsed laser system. Emission quantum yields were measured using a degassed acetonitrile solution of [Ru(bpy)3](PF6)2 (bpy=2,2′-bipyridine) as the standard (φr=0.062) and calculated by φs=φr(Br/Bs)(ns/nr)2(Ds/Dr), where the subscripts s and r refer to the sample and reference standard solution, respectively, n is the refractive index of the solvents, D is the integrated intensity, and φ is the luminescence quantum yield. The quantity B is calculated by B=1−10−AL, where A is the absorbance at the excitation wavelength and L is the optical path length. Errors for wavelength values (1 nm) and φ (10%) are estimated.
4-Methyl-2-bromoanisole and 4-(tert-butyl)-2-bromoanisole were prepared from 4-Methyl-2-bromophenol and 4-(tert-butyl)-2-bromophenol by reaction with MeI in the presence of K2CO3 following literature procedure. (Lygo, Tetrahedron Lett., 1999, 40, 1389)
84% 1H-NMR (400 MHz, CDCl3) δ (ppm) 7.36 (d, J=2.1 Hz, 1H), 7.05 (dd, J=8.3 Hz, 2.1 Hz, 1H), 6.79 (d, J=8.3 Hz, 1H), 3.86 (s, 3H), 2.28 (s, 3H)
1H-NMR (300 MHz, CDCl3) δ(ppm) 7.54 (d, J=2.2 Hz, 1H), 7.27 (dd, J=8.6 Hz, 2.2 Hz, 1H), 6.83 (d, J=8.6 Hz, 1H), 3.87 (s, 3H), 1.28 (s, 9H).
To a degassed DMSO (20 mL) solution of imidazole (1.0 g, 15 mmol) was added 2-bromoanisole (1.25 mL, 10 mmol), KOH (1.12 g, 20 mmol) and Cu2O (280 mg, 2 mmol) under nitrogen. The resulting mixture was stirred at 140° C. for 24 hrs under N2. After cooling to room temperature, the mixture was poured into ethylacetate (EA) (50 mL) and filtered. The filtrate was washed with water (50 mL×3) and dried over anhydrous magnesium sulfate. After rotary evaporation, the crude oil was purified via column chromatography on silica gel with eluent of EA/MeOH (9/1, v/v), affording a light yellow liquid (50%). 1H-NMR (400 MHz, CDCl3) δ(ppm) 7.79 (s, 1H), 7.36 (t, J=7.8 Hz, 1H), 7.28 (d, J=7.8 Hz, 1H), 7.21 (s, 1H), 7.17 (s, 1H), 7.05 (m, 2H), 3.85 (s, 3H).
To a degassed DMSO (20 mL) solution of imidazole (1.0 g, 15 mmol) was added 4-fluoro-2-bromoanisole (1.25 mL, 10 mmol), KOH (1.12 g, 20 mmol) and Cu2O (280 mg, 2 mmol) under nitrogen. The resulting mixture was stirred at 140° C. for 24 hrs under N2. After cooling to room temperature, the mixture was poured into ethylacetate (EA) (50 mL) and filtered. The filtrate was washed with water (50 mL×3) and dried over anhydrous magnesium sulfate. After rotary evaporation, the crude oil was purified via column chromatography on silica gel with eluent of EA/MeOH (9/1, v/v), affording a light yellow liquid (47%). 1H-NMR (400 MHz, CDCl3) δ(ppm) 7.82 (s, 1H), 7.21 (m, 1H), 7.17 (m, 1H), 7.07 (m, 2H), 7.00 (m, 1H), 3.84 (s, 3H).
To a degassed DMSO (20 mL) solution of imidazole (1.0 g, 15 mmol) was added 4-methyl-2-bromoanisole (1.25 mL, 10 mmol), KOH (1.12 g, 20 mmol) and Cu2O (280 mg, 2 mmol) under nitrogen. The resulting mixture was stirred at 140° C. for 24 hrs under N2. After cooling to room temperature, the mixture was poured into ethylacetate (EA) (50 mL) and filtered. The filtrate was washed with water (50 mL×3) and dried over anhydrous magnesium sulfate. After rotary evaporation, the crude oil was purified via column chromatography on silica gel with eluent of EA/MeOH (9/1, v/v), affording a light yellow solid (57%). 1H-NMR (300 MHz, CDCl3) δ(ppm) 7.78 (s, 1H), 7.16 (m, 3H), 7.09 (d, J=1.8 Hz, 1H), 6.94 (d, J=8.4 Hz, 1H), 3.81 (s, 3H), 2.33 (s, 3H).
To a degassed DMSO (20 mL) solution of imidazole (1.0 g, 15 mmol) was added 4-methyl-2-bromoanisole (1.25 mL, 10 mmol), KOH (1.12 g, 20 mmol) and Cu2O (280 mg, 2 mmol) under nitrogen. The resulting mixture was stirred at 140° C. for 24 hrs under N2. After cooling to room temperature, the mixture was poured into ethylacetate (EA) (50 mL) and filtered. The filtrate was washed with water (50 mL×3) and dried over anhydrous magnesium sulfate. After rotary evaporation, the crude oil was purified via column chromatography on silica gel with eluent of EA/MeOH (9/1, v/v), affording a light yellow oil with yield of 47%. 1H-NMR (400 MHz, CDCl3) δ(ppm) 7.77 (s, 1H), 7.37 (dd, J1=8.6 Hz, J2=2.4 Hz, 1H), 7.27 (d, J=2.4 Hz, 1H), 7.21 (1H), 7.17 (1H), 6.99 (d, J=8.6 Hz, 1H), 3.82 (s, 3H), 1.32 (s, 9H).
A solution of 2-(1H-imidazol-1-yl)anisole (0.82 g, 4.7 mmol) and dibromomethane (1 mL, 14 mmol) in THF (5 mL) was refluxed at 110° C. for 48 hrs. After cooling to room temperature, the resulting white precipitate was collected by filtration with suction, washed with THF, and air-dried to yield 0.9 g of solids (73%). 1H-NMR (400 MHz, DMSO-d6) δ(ppm) 10.01 (s, 2H), 8.30 (m, 2H), 8.22 (m, 2H), 7.64 (m, 4H), 7.41 (d, J=8.3 Hz, 2H), 7.22 (t, J=7.7 Hz, 2H), 6.90 (s, 2H), 3.90 (s, 6H).
A solution of 4-fluoro-2-(1H-imidazol-1-yl)anisole (0.90 g, 4.7 mmol) and dibromomethane (1 mL, 14 mmol) in THF (5 mL) was refluxed at 110° C. for 48 hrs. After cooling to room temperature, the resulting white precipitate was collected by filtration with suction, washed with THF, and air-dried to yield a white solid with yield of 70%. 1H-NMR (400 MHz, MeOD) δ(ppm) 8.33 (d, J=2.1 Hz, 2H), 8.11 (d, J=2.1 Hz, 2H), 7.66 (m, 2H), 7.40 (m, 4H), 7.11 (s, 2H), 3.98 (s, 6H). Note: the imidazole NCHN signal do not appeared in MeOD solvent.
A solution of 4-methyl-2-(1H-imidazol-1-yl)anisole (0.88 g, 4.7 mmol) and dibromomethane (1 mL, 14 mmol) in THF (5 mL) was refluxed at 110° C. for 48 hrs. After cooling to room temperature, the resulting white precipitate was collected by filtration with suction, washed with THF, and air-dried to yield a white solid with yield of 70%. 1H-NMR (300 MHz, DMSO-d6) δ(ppm) 9.93 (s, 2H), 8.26 (m, 2H), 8.20 (m, 2H), 7.47 (d, J=1.6 Hz, 2H), 7.44 (dd, J1=8.6 Hz, J2=1.6 Hz, 2H), 7.31 (d, J=8.6 Hz, 2H), 6.86 (s, 2H), 3.88 (s, 3H), 2.33 (s, 3H).
A solution of 4-t-butyl-2-(1H-imidazol-1-yl)anisole (1.08 g, 4.7 mmol) and dibromomethane (1 mL, 14 mmol) in THF (5 mL) was refluxed at 110° C. for 48 hrs. After cooling to room temperature, the resulting white precipitate was collected by filtration with suction, washed with THF, and air-dried to yield a white solid with yield of 74%. 1H-NMR (400 MHz, DMSO-d6) δ(ppm) 10.00 (s, 2H), 8.31 (m, 2H), 8.24 (m, 2H), 7.64 (m, 4H), 7.33 (d, J=8.8 Hz, 2H), 6.89 (s, 2H), 3.89 (s, 3H), 1.28 (s, 18H).
A solution of 1,1′-bis[(2-methoxyphenyl)-1H-imidazolium]-3,3′-methanediyl dibromide (0.81 g, 1.55 mmol) in HBr (48 wt. % aq. 6.5 mL)/HOAc (6.5 mL) was heated to reflux at 120° C. for 48 hrs. After reaction, the mixture was rotary evaporated. Acetone was added to the residue to induce precipitation of brown solids, which were collected by filtration and washed with EA. After reprecipitation from DMF/EA, a white solid was obtained (0.52 g, 68%). 1H-NMR (400 MHz, DMSO-d6) δ(ppm) 11.08 (br s, 2H), 9.99 (s, 2H), 8.29 (s, 2H), 8.22 (s, 2H), 7.57 (d, J=7.86 Hz, 2H), 7.44 (t, J=7.77 Hz, 2H), 7.19 (d, J=8.13 Hz, 2H), 7.06 (t, J=7.58 Hz, 2H), 6.90 (s, 2H).
A solution of 1,1′-bis[(4-fluoro-2-methoxyphenyl)-1H-imidazolium]-3,3′-methanediyl dibromide (0.87 g, 1.55 mmol) in HBr (48 wt. % aq. 6.5 mL)/HOAc (6.5 mL) was heated to reflux at 120° C. for 48 hrs. After reaction, the mixture was rotary evaporated. Acetone was added to the residue to induce precipitation of brown solids, which were collected by filtration and washed with EA. After reprecipitation from MeOH/EA, a white solid was obtained with yield of 84% 1H-NMR (300 MHz, MeOD) δ(ppm) 9.97 (im NCHN, s, active), 8.23 (d, J=2.0 Hz, 2H), 8.13 (d, J=2.0 Hz, 2H), 7.52 (dd, J1=8.4 Hz, J2=3.0 Hz, 2H), 7.26 (td, J1=9.0 Hz, J2=3.0 Hz, 2H), 7.14 (dd, J1=9.0 Hz, J2=4.8 Hz, 2H), 7.00 (s, 2H).
A solution of 1,1′-bis[(4-methyl-2-methoxyphenyl)-1H-imidazolium]-3,3′-methanediyl dibromide (0.85 g, 1.55 mmol) in HBr (48 wt. % aq. 6.5 mL)/HOAc (6.5 mL) was heated to reflux at 120° C. for 48 hrs. After reaction, the mixture was rotary evaporated. Acetone was added to the residue to induce precipitation of brown solids, which were collected by filtration and washed with EA. After reprecipitation from MeOH/EA, a white solid was obtained with yield of 65% 1H-NMR (300 MHz, DMSO-d6) δ(ppm) 10.82 (br s, 2H), 9.96 (s, 2H), 8.28 (m, 2H), 8.20 (m, 2H), 7.39 (d, J=1.6 Hz, 2H), 7.25 (dd, J1=8.4 Hz, J2=1.6 Hz, 2H), 7.08 (d, J=8.4 Hz, 2H), 6.88 (s, 2H), 2.28 (s, 6H). (300 MHz, MeOD) δ(ppm) 9.91 (im NCHN, s, 2H), 8.20 (m, 2H), 8.09 (m, 2H), 7.43 (d, J=1.6 Hz, 2H), 7.28 (dd, J1=8.4 Hz, J2=1.6 Hz, 2H), 7.03 (d, J=8.4 Hz, 2H), 6.98 (s, 2H), 2.35 (s, 6H).
A solution of 1,1′-bis[(4-t-butyl-2-methoxyphenyl)-1H-imidazolium]-3,3′-methanediyl dibromide (0.98 g, 1.55 mmol) in HBr (48 wt. % aq. 6.5 mL)/HOAc (6.5 mL) was heated to reflux at 120° C. for 48 hrs. After reaction, the mixture was rotary evaporated. Acetone was added to the residue to induce precipitation of brown solids, which were collected by filtration and washed with EA. After reprecipitation from DMF/EA, a white solid was obtained with yield of 62%. 1H-NMR (400 MHz, DMSO) δ(ppm) 10.85 (s, 2H), 9.91 (s, 2H), 8.24 (m, 4H), 7.48 (m, 4H), 7.11 (d, J=8.4 Hz), 6.84 (s, 2H), 1.29 (s, 18H).
A mixture of 1,1′-bis[(2-hydroxyphenyl)-1H-imidazolium]-3,3′-methanediyl dibromide (193 mg, 0.39 mmol), Pt(DMSO)2Cl2 (164 mg, 0.39 mmol) and Et3N (0.325 mL, 6 eq.) in EtOH (20 mL) was heated to 80° C. for 6 hrs. After completion of reaction, the mixture was cooled to room temperature, collected by centrifugation, washed with ethanol, ether and was dried under vacuum, affording pale yellow solids (60%). 1H-NMR (400 MHz, DMSO-d6) δ(ppm) 8.34 (d, J=2.3 Hz, 2H), 7.71 (d, J=2.3 Hz, 2H), 7.69 (d, J=8.35 Hz, 2H), 7.06 (t, J=7.65 Hz, 2H), 6.92 (d, J=8.27 Hz, 2H), 6.57 (t, J=7.57 Hz, 2H), 6.31 (s, 2H) FAB-MS: 526.0 [M+H]+. Anal. Calcd. For C19H14N4O2Pt.H2O: C, 41.99; H, 2.97; N, 10.31. Found: C, 42.06; H, 2.88; N, 9.99.
A mixture of 1 (207 mg, 0.39 mmol), Pt(DMSO)2Cl2 (164 mg, 0.39 mmol) and Et3N (0.325 mL, 6 eq.) in EtOH (20 mL) was heated to 80° C. for 6 hrs. After completion of reaction, the mixture was cooled to room temperature, collected by centrifugation, washed with ethanol, ether and was dried under vacuum, affording white solids with yield of 49%. 1H-NMR (400 MHz, DMSO-d6) δ(ppm) 8.34 (d, J=1.8 Hz, 2H), 7.72 (d, J=1.8 Hz, 2H), 7.66 (d, J=10.5 Hz, 2H), 6.90 (m, 4H), 6.32 (s, 2H) FAB-MS: 561.0 [M+H]+. Anal. Calcd. For C19H12N4O2Pt.H2O: C, 39.38; H, 2.44; N, 9.67. Found: C, 38.77; H, 2.40; N, 9.35.
A mixture of 2 (204 mg, 0.39 mmol), Pt(DMSO)2Cl2 (164 mg, 0.39 mmol) and Et3N (0.325 mL, 6 eq.) in EtOH (20 mL) was heated to 80° C. for 6 hrs. After completion of reaction, the mixture was cooled to room temperature, collected by centrifugation, washed with ethanol, ether and was dried under vacuum, affording white solids with yield of 56%. 1H-NMR (300 MHz, DMSO-d6) δ(ppm) 8.31 (d, J=2.1 Hz, 2H), 7.69 (d, J=2.1 Hz, 2H), 7.51 (s, 2H), 6.87 (d, J=8.2 Hz, 2H), 6.80 (d, J=8.2 Hz, 2H), 6.29 (s, 2H), 2.25 (s, 6H) FAB-MS: 553.0 [M+H]+. Anal. Calcd. For C21H18N4O2Pt.CH2Cl2: C, 41.39; H, 3.16; N, 8.78. Found: C, 41.38; H, 3.22; N, 8.82.
A single-crystal of 5 suitable for X-ray diffraction analysis was obtained from a dilute solution in dichloromethane upon slow evaporation of the solvent in the presence of air. The complex crystallized into an orthorhombic space group, as indicated in Table 1, below. As can be seen in
aR = Σ||Fo| − |Fc||/Σ|Fo|.
bRw = [Σ w (|Fo| − |Fc|)2/Σ w |Fo|2]1/2.
A mixture of 3 (237 mg, 0.39 mmol), Pt(DMSO)2Cl2 (164 mg, 0.39 mmol) and Et3N (0.325 mL, 6 eq.) in EtOH (20 mL) was heated to 80° C. for 6 hrs. After completion of reaction, the mixture was cooled to room temperature, collected by centrifugation, washed with ethanol, ether and was dried under vacuum, affording white solids with yield of 58%. 1H-NMR (400 MHz, DMSO-d6) δ(ppm) 8.42 (d, 2.3 Hz, 2H), 7.71 (d, 2.3 Hz, 2H), 7.52 (d, J=2.3 Hz, 2H), 7.08 (dd, J1=8.6 Hz, J2=2.3 Hz, 2H), 6.83 (d, J=8.6 Hz, 2H), 6.30 (s, 2H), 1.29 (s, 18H) FAB-MS: 638.2 [M+H]+. Anal. Calcd. For C27H30N4O2Pt.H2O: C, 49.46; H, 4.92; N, 8.55. Found: C, 49.36; H, 4.64; N, 8.46.
Absorption and emission spectra were acquired for complexes 4-7, as summarized in Table 2, below, solution measurements were performed using THF-DMF (19:1, v/v) solutions. All of the complexes show a vibronically structured absorption band with peak maxima at about 350 nm and molar extinction coefficients of about 1×104 M−1 cm−1. In solution, complexes 5 and 6 display structure-less emissions centered at around 460 nm with quantum yields of 8% and lifetimes of 1.8 μs, which is significantly greater than that for 7, the complex from an unsubstituted ligand. A blue-shifted emission maximum at 443 nm with a high quantum yield of 18% and long lifetime of 3.5 μs was observed in solution for complex 4 with an electron-drawing fluoride group para to the phenolate oxygen. A red-shift of 5 nm for the emission maxima for 4-7 was observed upon changing solvent from THF-DMF to dichloromethane-DMF (19:1, v/v). Representative adsorption and emission spectra for 4-6 are shown in
Complexes 4-7 are highly emissive in the blue spectral region when measured in films prepared by the dispersion of a complex in an inert polymer matrix, poly(methyl methacrylate) (PMMA) in these exemplary examples, at a complex to polymer weight ratio as low as 1%. Absolute emission quantum yields for these solid films, measured by an integrate sphere method, were observed to be approximately 30%, within experimental error, at room temperature for 4-7 with emission maxima blue-shifted by 10 nm from that recorded for the complexes in THF-DMF solution, which suggests a solid-solution state within the film. All of the films exhibit emission with a chromaticity of CIEx,y<0.2 (CIEx,y=Commission Internationale de L'Eclairage coordinates) and CIEx+y<0.3, and particularly, films of complex 4 gave CIEx,y at (0.15, 0.10), being close to an ideal deep blue with CIEx,y at (0.14, 0.10).
[a]Recorded in degassed THF-DMF (19:1, v/v) solutions with a concentration of ~2 × 10−5 M, absorption at about 305 is a shoulder, and λex for emissions is 350 nm.
[b]Recorded in 1% PMMA film and λex for emissions is 350 nm.
Decomposition temperatures of 4-6 under a nitrogen atmosphere are 410, 390, and 400° C., respectively, as deteunined by thermogravimetric analyses, as shown in
Complex 6 was used as phosphorescent dopant in a blue OLED. The device configuration is ITO/2-TNATA (40 nm)/NPB (20 nm)/DP4-Pt 3% (30 nm)/TPBi (40 nm)/LiF (0.5 nm)/Al (100 nm). 2-TNATA, NPB and TPBi were used as hole-injection layer (HIL), hole-transporting layer (HTL) and electron-transporting layer (ETL), respectively. The host DP4 was obtained from Aglaia Tech. Beijing, China, and its chemical structure cannot be revealed due to patent consideration. All materials were thermal-deposited in high vacuum in succession without breaking the vacuum. After finishing the whole deposition, the device was encapsulated with glass cap and tested at ambient conditions. The electroluminescence was recorded by a PR650-spectrometer and K2400 as the voltage source.
An OLED was fabricated using 6, which was vacuum-deposited as a dopant into the emitting layer of an OLED with a configuration of ITO/2-TNATA (40 nm)/NPB (20 nm)/DP4-Complex 102 (30 nm)/TPBi (40 nm)/LiF (0.5 nm)/Al (100 nm). 2-TNATA, NPB and TPBi, whose structures are shown in
It should be understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and the scope of the appended claims. In addition, any elements or limitations of any invention or embodiment thereof disclosed herein can be combined with any and/or all other elements or limitations (individually or in any combination) or any other invention or embodiment thereof disclosed herein, and all such combinations are contemplated with the scope of the invention without limitation thereto.
This application claims the benefit of U.S. Provisional Application Ser. No. 61/491,711, filed May 31, 2011, which is hereby incorporated by reference in its entirety including any tables, figures, or drawings.
| Number | Date | Country |
|---|---|---|
| WO 2006058535 | Jun 2006 | WO |
| Entry |
|---|
| Yagyu et al. “Synthesis and Characterization of a Manganese(III) Complex with a Tetradentate N-Heterocyclic Carbene Ligand” Organometallics, 2009, vol. 28, pp. 2342-2344. |
| Li et al. “Blue electrophosphorescent organoplatinum(II) complexes with dianionic tetradentate bis(carbene) ligands ” Chemical Communications, 2011, vol. 47, pp. 9075-9077 plus 20 pages of supporting information. |
| Number | Date | Country | |
|---|---|---|---|
| 20120309979 A1 | Dec 2012 | US |
| Number | Date | Country | |
|---|---|---|---|
| 61491711 | May 2011 | US |
