435293-93-9

Basic information

• Product Name: Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III)
• Synonyms: Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III);Tris[1-phenylisoquinoline-C2,N]iridium(III);tris(2-(isoquinolin-1-yl)phenyl)iridium;Tris[1-phenylisoquinoline-C2,N]iridium(III) (purified by sublimation);Tris[1-phenylisoquinolinato-C2,N]iridiuM(III);Ir(piq)3 , Tris(1-phenylisoquinoline) iridiuM(III);(piq)3Ir;Tris[1-phenylisoquinoline-C2,N]iridiuM(III)
• CAS NO: 435293-93-9
• Molecular Formula: C45H30IrN3
• Molecular Weight: 804.973
• Product Categories: oled materials;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, functional materials
• Mol File: 435293-93-9.mol

Chemical Properties

• Melting Point: 454 °C
• Appearance: /
• CAS DataBase Reference: Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III)(CAS DataBase Reference)
• NIST Chemistry Reference: Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III)(435293-93-9)
• EPA Substance Registry System: Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III)(435293-93-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 435293-93-9(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III) is used as a catalyst in the Suzuki reaction, a widely employed cross-coupling reaction in organic chemistry. This reaction allows for the formation of carbon-carbon bonds between an organoboron compound and an organohalide, leading to the synthesis of various organic compounds.
Used in Optoelectronics Industry:
Due to its deep red phosphorescence, Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III) can be utilized in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its unique optical properties make it a promising candidate for improving the performance and efficiency of these devices.
Used in Medicinal Chemistry:
Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III) may also find applications in medicinal chemistry, particularly in the design and synthesis of new pharmaceutical compounds. Its unique properties could potentially be harnessed to develop novel drugs with improved efficacy and selectivity.
Used in Environmental Applications:
The catalytic properties of Ir(piq)3, Tris[1-phenylisoquinolinato-C2,N]iridium(III) can be employed in environmental applications, such as the degradation of pollutants and the development of green chemistry processes. Its ability to catalyze reactions under mild conditions could contribute to more sustainable and eco-friendly chemical processes.

Classification

Organometallic iridium complex, Red emitter, Phosphorescence dopant OLEDs, Sublimed materials.

InChI:InChI=1/3C15H10N.Ir/c3*1-2-7-13(8-3-1)15-14-9-5-4-6-12(14)10-11-16-15;/h3*1-7,9-11H;/rC45H30IrN3/c1-4-16-34-31(13-1)25-28-47-43(34)37-19-7-10-22-40(37)46(47,41-23-11-8-20-38(41)44-35-17-5-2-14-32(35)26-29-48(44)46)42-24-12-9-21-39(42)45-36-18-6-3-15-33(36)27-30-49(45)46/h1-30H