Skip to Content
Merck
All Photos(2)

Documents

688096

Sigma-Aldrich

Tris[2-phenylpyridinato-C2,N]iridium(III)

97%

Synonym(s):

Ir(ppy)3, Iridium, tris[2-(2-pyridinyl-κN)phenyl-κC]

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C33H24IrN3
CAS Number:
Molecular Weight:
654.78
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

description

fac-Tris[2-phenylpyridinato-C2,N]iridium(III)

Assay

97%

form

powder

reaction suitability

core: iridium
reaction type: Photocatalysis
reagent type: catalyst

photocatalyst activation

425 nm

fluorescence

λex 340 nm; λem 512 nm in chloroform

Orbital energy

HOMO 5.6 eV 
LUMO 3 eV 

OLED Device Performance

ITO/HMPD/TAZ:Ir(ppy)3 (7%)/Alq3/Al:Li

  • Color: green
  • Max. Luminance: 4000 Cd/m2
  • Max. EQE: 15 %

ITO/NPD/CBP:Ir(ppy)3 (6%)/Alq3/Mg:Ag
  • Color: green
  • Max. Luminance: 100000 Cd/m2
  • Max. EQE: 8 %
  • Turn-On Voltage: 4.3 V

ITO/NPD/TCTA/BCPO:Ir(ppy)3 (7-8%)/BCP/Alq3/LiF/Al
  • Color: green
  • Max. Luminance: 207839 Cd/m2
  • Max. EQE: 21.6 %
  • Turn-On Voltage: 2.1 V

ITO/TCTA/Ir(ppy)3/Bphen/LiF/Al
  • Color: green
  • Max. Luminance: 300000 Cd/m2
  • Max. EQE: 19 %
  • Turn-On Voltage: 2.6 V

SMILES string

c1ccc(nc1)-c2ccccc2[Ir](c3ccccc3-c4ccccn4)c5ccccc5-c6ccccn6

InChI

1S/3C11H8N.Ir/c3*1-2-6-10(7-3-1)11-8-4-5-9-12-11;/h3*1-6,8-9H;

InChI key

QKBWDYLFYVXTGE-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

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.

Application

Learn More at the Professor and Product Portal of Professor Corey Stephenson.
Put to elegant use by Stephenson for the reduction of alkyl, alkenyl and aryl iodides in the presence of visible light. Intramolecular reductive cyclizations were also achieved with this catalyst.

Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Theoretical study on the absorption spectra of fac-Ir (ppy) 3 in the amorphous phase of organic electro-luminescent devices.
Asada T, et al.
Research on Chemical Intermediates, 35(8-9), 851-863 (2009)
Tuning the emission of cyclometalated iridium complexes by simple ligand modification
Ifor DW, et al.
Journal of Materials Chemistry, 13(1), 80-83 (2003)
High-efficiency, low-voltage phosphorescent organic light-emitting diode devices with mixed host
Kondakova, M.; Pawlik, T.; Young, R.; et al.
Journal of Applied Physics, 104, 094501-094501 (2008)
Highly efficient, single-layer organic light-emitting devices based on a graded-composition emissive layer
Holmes, R. J.; et al.
Applied Physics Letters, 97, 083308-083308 (2010)
High-efficiency organic electrophosphorescent devices with tris(2-phenylpyridine)iridium doped into electron-transporting materials
Adachi, C.; ea al.
Applied Physics Letters, 77, 904-904 (2000)

Articles

In this article, we demonstrate that bis-styrylbenzene derivatives show promising characteristics for very low lasing thresholds and discuss the design considerations for organic lasing molecules.

Related Content

Research in the Stephenson lab focuses upon the development of new chemical methods which enable the activation of chemical bonds under mild reaction conditions.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service