Na et al., 2018 - Google Patents
Highly luminescent cyclometalated iridium complexes generated by nucleophilic addition to coordinated isocyanidesNa et al., 2018
- Document ID
- 1083814681812675441
- Author
- Na H
- Teets T
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
In this work, we report a new class of blue-emitting cyclometalated iridium complexes supported by acyclic diaminocarbene (ADC) ancillary ligands. These neutral, tris-chelated complexes are not obtainable via traditional synthesis routes and instead are generated …
- 150000002503 iridium 0 title abstract description 45
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0033—Iridium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0073—Rhodium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0086—Platinum compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0077—Coordination compounds, e.g. porphyrin
- H01L51/0084—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H01L51/0085—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising Iridium
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/185—Metal complexes of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
- C07F5/02—Boron compounds
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0077—Coordination compounds, e.g. porphyrin
- H01L51/0089—Metal complexes comprising Lanthanides or Actinides, e.g. Eu
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/50—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes [OLED] or polymer light emitting devices [PLED];
- H01L51/5012—Electroluminescent [EL] layer
- H01L51/5016—Triplet emission
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Na et al. | Highly luminescent cyclometalated iridium complexes generated by nucleophilic addition to coordinated isocyanides | |
Lamansky et al. | Synthesis and characterization of phosphorescent cyclometalated iridium complexes | |
Sajoto et al. | Temperature dependence of blue phosphorescent cyclometalated Ir (III) complexes | |
Turner et al. | Cyclometalated platinum complexes with luminescent quantum yields approaching 100% | |
Fernández-Hernández et al. | Control of the mutual arrangement of cyclometalated ligands in cationic iridium (III) complexes. Synthesis, spectroscopy, and electroluminescence of the different isomers | |
Czerwieniec et al. | Blue-light emission of Cu (I) complexes and singlet harvesting | |
Chen et al. | Rational design of strongly blue-emitting cuprous complexes with thermally activated delayed fluorescence and application in solution-processed OLEDs | |
Li et al. | Synthetic control of excited-state properties in cyclometalated Ir (III) complexes using ancillary ligands | |
Brulatti et al. | Luminescent Iridium (III) Complexes with N∧ C∧ N-Coordinated Terdentate Ligands: Dual Tuning of the Emission Energy and Application to Organic Light-Emitting Devices | |
Liu et al. | Synthesis and electrophosphorescence of iridium complexes containing benzothiazole-based ligands | |
Li et al. | Metal-assisted delayed fluorescent Pd (II) complexes and phosphorescent Pt (II) complex based on [1, 2, 4] triazolo [4, 3-a] pyridine-containing ligands: synthesis, characterization, electrochemistry, photophysical studies, and application | |
Liu et al. | “Click” synthesis of heteroleptic tris-cyclometalated iridium (III) complexes: Cu (I) triazolide intermediates as transmetalating reagents | |
Adamovich et al. | Preparation of tris-heteroleptic iridium (III) complexes containing a cyclometalated aryl-N-heterocyclic carbene ligand | |
Pal et al. | Blue-to-green emitting neutral Ir (III) complexes bearing pentafluorosulfanyl groups: a combined experimental and theoretical study | |
Tamura et al. | Efficient Synthesis of Tris-Heteroleptic Iridium (III) Complexes Based on the Zn2+-Promoted Degradation of Tris-Cyclometalated Iridium (III) Complexes and Their Photophysical Properties | |
Tamura et al. | Stereospecific synthesis of tris-heteroleptic tris-cyclometalated Iridium (III) complexes via different heteroleptic halogen-bridged iridium (III) dimers and their photophysical properties | |
Takayasu et al. | Intermolecular Interactions and Aggregation of fac-Tris (2-phenylpyridinato-C 2, N) iridium (III) in Nonpolar Solvents | |
Dedeian et al. | Blue Phosphorescence from Mixed Cyano− Isocyanide Cyclometalated Iridium (III) Complexes | |
Adamovich et al. | Preparation via a NHC dimer complex, photophysical properties, and device performance of heteroleptic bis (tridentate) iridium (III) emitters | |
Chaaban et al. | Thiazol-2-thiolate-bridged binuclear platinum (II) complexes with high photoluminescence quantum efficiencies of up to near unity | |
Na et al. | Photoluminescence of cyclometalated iridium complexes in poly (methyl methacrylate) films | |
Wang et al. | Cationic iridium complexes with 5-phenyl-1 H-1, 2, 4-triazole type cyclometalating ligands: toward blue-shifted emission | |
Cudré et al. | Tris-heteroleptic iridium complexes based on cyclometalated ligands with different cores | |
Mandapati et al. | Deep-red luminescence from platinum (II) complexes of N^ N–^ N-amido ligands with benzannulated N-heterocyclic donor arms | |
Liao et al. | Iridium (III) complexes bearing tridentate chromophoric chelate: phosphorescence fine-tuned by phosphine and hydride ancillary |