4,5-Diazafluoren-9-one behaves like cyclopentadienones and reacts with [Cp*Co(C2H4)2] to form air -stable sandwich-type complexes [Cp*Co(η4-2)].
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4,5-Diazafluoren-9-one behaves like cyclopentadienones and reacts with [Cp*Co(C2H4)2] to form air -stable sandwich-type complexes [Cp*Co(η4-2)].
Solubility
Soluble in dichloromethane, tetrahydrofuran, chloroform, benzene, toluene and polar organic solvents. Insoluble in diethyl ether and alkanes.
Notes
Incompatible with strong oxidizing agents. Avoid heat and source of ignition.
RUO – Research Use Only
Piotrowicz, M.; Zakrzewski, J.; Metivier, R.; Brosseau, A.; Makal, A.; Wozniak, K. Aerobic Palladium(II)-Catalyzed Dehydrogenative Heck Reaction in the Synthesis of Pyrenyl Fluorophores. A Photophysical Study of β-Pyrenyl Acrylates in Solution and in the Solid State. J. Org. Chem. 2015, 80 (5), 2573-2581.
Liu, B.; Shi, B. Transition-metal-catalyzed etherification of unactivated C H bonds. Tetrahedron Lett. 2015, 56 (1), 15-22.