Reacción #2122502

ord-677a8fbbf6994d90b5c394a5b47fe31f

Ecuación de reacción

O=C(O)c1ccccn1
picolinic acid
[Cl][Ir]([Cl])[Cl].c1ccc(-c2nc3ccccc3o2)cc1
2-phenylbenzoxazole Iridium chloride
O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.[Ir+3].c1ccc(-c2nc3ccccc3o2)cc1.c1ccc(-c2nc3ccccc3o2)cc1
Bis(2-phenylbenzooxazole) Iridium picolinate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was heated
  2. 2
    Temperaturato reflux under nitrogen in an oil bath overnight (17.5 hrs.)
  3. 3
    OtroReaction mixture
  4. 4
    Filtraciónthe yellow precipitate was filtered off via vacuum
  5. 5
    workup.DISSOLUTIONThe precipitate was dissolved in dichloromethane
  6. 6
    Otrowas removed

Procedimiento

0.52 mmol (0.064 g) of picolinic acid was added to a room-temperature solution of 0.14 mmol 2-phenylbenzoxazole Iridium chloride dimer (0.18 g) in 20 mL of dichloromethane. The mixture was heated to reflux under nitrogen in an oil bath overnight (17.5 hrs.). Reaction mixture was cooled to room temperature, and the yellow precipitate was filtered off via vacuum. The precipitate was dissolved in dichloromethane and transferred to a vial, and the solvent was removed. Emission spectrum is in FIG. 46.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08574726B2uspto-grants-2013_11