反应 #2122502

ord-677a8fbbf6994d90b5c394a5b47fe31f

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The mixture was heated
  2. 2
    温度to reflux under nitrogen in an oil bath overnight (17.5 hrs.)
  3. 3
    其他Reaction mixture
  4. 4
    过滤the yellow precipitate was filtered off via vacuum
  5. 5
    workup.DISSOLUTIONThe precipitate was dissolved in dichloromethane
  6. 6
    其他was removed

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08574726B2uspto-grants-2013_11