- Fac-Ir (ppy)3
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2026-05-19
- CAS:94928-86-6
- Min. Order: 1g
- Purity: 99.90%
- Supply Ability: 100kgs
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| Product Name: | Tris(2-phenylpyridine)iridium (Ir(ppy)3) | | Synonyms: | Tris(2-phenylpyridinato) iridium(III),98+%;TRIS(2-PHENYLPYRIDINE)IRIDIUM (III);Tris[2-phenylpyridinato-C2,N]iridium(III) sublimed grade;Tris(2-phenylpyridine)iridium (Ir(ppy)3);iridium(3+),2-phenylpyridine;Iridium, tris(2-phenylpyidine);Tris(2-phenylpyridinato)iridium(III), 98%, purified by sublimation;Tris(2-phenylpyridine) | | CAS: | 94928-86-6 | | MF: | C33H24IrN3 | | MW: | 654.79 | | EINECS: | 635-640-5 | | Product Categories: | Electronic Chemicals;electronic;Classes of Metal Compounds;Highly Purified Reagents;Ir (Iridium) Compounds;Other Categories;Refined Products by Sublimation;Transition Metal Compounds;olde Materials;oled materials;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, functional materials;OLED;94928-86-6 | | Mol File: | 94928-86-6.mol |  |
| | Tris(2-phenylpyridine)iridium (Ir(ppy)3) Chemical Properties |
| Melting point | 328°C | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | form | Powder | | color | yellow | | Sensitive | air sensitive | | λmax | 282 nm | | InChI | InChI=1S/3C11H8N.Ir/c3*1-2-6-10(7-3-1)11-8-4-5-9-12-11;/h3*1-6,8-9H; | | InChIKey | QKBWDYLFYVXTGE-UHFFFAOYSA-N | | SMILES | C1C=CC(C2C=CC=CC=2[Ir](C2C(C3N=CC=CC=3)=CC=CC=2)C2C=CC=CC=2C2N=CC=CC=2)=NC=1 | | CAS DataBase Reference | 94928-86-6(CAS DataBase Reference) | | Absorption | λmax282, 377 nmin THF |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26 | | WGK Germany | 3 | | TSCA | No | | HS Code | 28439000 | | Storage Class | 11 - Combustible Solids |
| Provider | Language |
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ALFA
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| | Tris(2-phenylpyridine)iridium (Ir(ppy)3) Usage And Synthesis |
| Applications | Tris(2-phenylpyridine)iridium(III), Ir(ppy)3, is used widely in organic light-emitting diodes (OLEDs) due to its high quantum yields and thermal stability.
Utilizing all of its singlet and triplet excitons for the emission, this green light emitting Ir(ppy)3 exhibits a very bright phosphorescence with an internal quantum yield of almost 100%. It is one of the most successful green-triplet emitters in the rapidly developing field of OLED display technology.
| | Reactions |
- Photocatalyst for ?-amino C–H arylation of cyano(hetero)arenes by tertiary amines
- Photocatalyst for trifluoromethylation of alkenes and alkynes
- Photocatalyst for reduction of alkyl, alkenyl, aryl iodides (a) and intramolecular reductive cyclizations (d)
- Photocatalyst for organocatalyst assisted direct arylation of allylic sp3 C–H bonds
- Photocatalyst for the generation multifluorinated biaryls via functionalization of the C−F bond of a perfluoroarene and C−H bond of the other arene in the presence of amines
- Photocatalyst for visible-light photoredox arylation of thiols with various aryl halides
| | Description | Tris(2-phenylpyridine)iridium(III), Ir(ppy)3, is used widely in organic light-emitting diodes (OLEDs) due to its high quantum yields and thermal stability. | | Chemical Properties | Light yellow to red solid | | Uses | suzuki reaction | | Uses | Tris(2-phenylpyridine)iridium can be useful as a photoredox catalyst in the preparation of fused-quinoxaline derivatives, difluorinated ketones and carbazoles. It can be a useful modifier in optogenetic control of behavior of larva expressing ChR2 in Drosophila melanogaster. It can also be useful in the development of a metal-containing nucleoside that possesses both therapeutic and diagnostic activity against cancer. | | General Description | Tris-(2-phenylpyridine) iridium [Ir(ppy)3] is a heavy metal complex. [Ir(ppy)3] is the most frequently used precursor molecule for the synthesis of electro-phosphorescent materials, which are then used in organic light emitting diodes (OLEDs). It provides green-color emission and high phosphorescence quantum yield close to unity. | | reaction suitability | core: iridium
reaction type: Photocatalysis
reagent type: catalyst | | Synthesis | fac-Tris(2-phenylpyridine)iridium derivatives containing hole-trapping moieties are synthesized, and deuterated tris(2-phenylpyridine)iridium is prepared using deuterated 2-phenylpyridine as a ligand[1][2]. | | References | [1]Ono, K., Joho, M., Saito, K., Tomura, M., Matsushita, Y., Naka, S., Okada, H., & Onnagawa, H. (2006). Synthesis and Electroluminescence Properties of fac-Tris(2-phenylpyridine)iridium Derivatives Containing Hole-Trapping Moieties. European Journal of Inorganic Chemistry, 2006(18), 3676–3683. https://doi.org/10.1002/ejic.200600285
[2]Wang, P., Wang, F.-F., Chen, Y., Niu, Q., Lu, L., Wang, H.-M., Gao, X.-C., Wei, B., Wu, H.-W., Cai, X., & Zou, D.-C. (2013). Synthesis of all-deuterated tris(2-phenylpyridine)iridium for highly stable electrophosphorescence: the “deuterium effect”. Journal of Materials Chemistry C, 1(32), 4821. https://doi.org/10.1039/c3tc30547c |
| | Tris(2-phenylpyridine)iridium (Ir(ppy)3) Preparation Products And Raw materials |
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