Réaction #2122502

ord-677a8fbbf6994d90b5c394a5b47fe31f

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe mixture was heated
  2. 2
    Températureto reflux under nitrogen in an oil bath overnight (17.5 hrs.)
  3. 3
    AutreReaction mixture
  4. 4
    Filtrationthe yellow precipitate was filtered off via vacuum
  5. 5
    workup.DISSOLUTIONThe precipitate was dissolved in dichloromethane
  6. 6
    Autrewas removed

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08574726B2uspto-grants-2013_11