Activation of methane with organopalladium complexes

Autor: Charles E. Taylor, Richard P. Noceti, R. Rox Anderson
Rok vydání: 1997
Předmět:
Zdroj: Catalysis Today. 35:407-413
ISSN: 0920-5861
DOI: 10.1016/s0920-5861(96)00213-1
Popis: Selective, direct oxidation of methane to methanol is a process of scientific interest and industrial importance. Reports have appeared in the literature describing the use of organometallic complexes to effect this transformation [1–5]. Investigation of one of these reaction schemes in our laboratory has produced interesting results. Our research effort was an extension of work reported by Sen et al. [3]. The reported reaction occurs between methane (at 800 psig 5.52 MPa) and palladium(II) acetate in trifluoroacetic acid at 80°C (Eq. (1)). The product, methyl trifluoroacetate, is readily hydrolyzed to produce methanol and trifluoroacetic acid. It is reported that methyl trifluoroacetate is produced with reported conversions, calculated on palladium metal recovery, of ∼ 60 percent. CH 4 + Pd(O 2 CCH 3 ) 2 → 80° C , 800 PSIG CF 3 COOH CF 3 CO 2 CH 3 + Pd .
Databáze: OpenAIRE