| Names | |
|---|---|
| Other names tris(2-phenylpyridine)iridium, Tris[2-(2-pyridinyl)phenyl]iridium, Tris[2-(2-pyridinyl)phenyl-C,N]iridium | |
| Identifiers | |
| |
| ChemSpider | |
| ECHA InfoCard | 100.163.509 |
PubChem CID |
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CompTox Dashboard (EPA) | |
| |
| Properties | |
| C33H24IrN3 | |
| Molar mass | 654.793 g·mol−1 |
| Appearance | yellow-green solid |
| Hazards | |
| GHS labelling: | |
| | |
| Warning | |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Tris(2-phenylpyridine)iridium, abbreviated [Ir(ppy)3] is the organoiridium complex with the formula Ir(C6H4-C5H4N)3. The complex, a yellow-green solid, is a derivative of Ir3+ bound to three monoanionic 2-pyridinylphenyl ligands. It is electroluminescent, emitting green light. The complex is observed with the facial stereochemistry, which is chiral.
The complex is prepared by cyclometalation reactions of 2-phenylpyridine and iridium trichloride, as represented by this idealized equation: [1] [2]
The complex and many analogues have been investigated for application in photoredox catalysis. Its excited state has an oxidative potential of −2.14 V, nearly 1 V more negative than the oxidative potential of excited [Ru(bipy)3]2+. [3]