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Carbon-Oxygen Bond Formation at Organopalladium Centers: The Reactions of PdMeR(L2) (R = Me, 4-tolyl; L2 = tmeda, bpy) with Diaroyl Peroxides and the Involvement of Organopalladium(IV) Species
Canty, AJ and Denney, MC and Skelton, BW and White, AH (2004) Carbon-Oxygen Bond Formation at Organopalladium Centers: The Reactions of PdMeR(L2) (R = Me, 4-tolyl; L2 = tmeda, bpy) with Diaroyl Peroxides and the Involvement of Organopalladium(IV) Species. Organometallics, 23. pp. 1122-1131.
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The group 16 oxidants dibenzoyl- and bis(4-trifluoromethylbenzoyl)-peroxide react with dimethylpalladium(II) and methyl(4-tolyl)palladium(II) complexes of the bidentate nitrogen donor ligands 2,2'-bipyridine and N,N,N'N'-tetramethylethylenediamine in discrete stepwise processes as the temperature is raised from -70 °C. Carbon-oxygen bonds are formed during this reaction sequence but not from those Pd(IV) complexes detected spectroscopically. The initial reaction gives undetected “PdIV(O2CAr)2MeR(L2)” (Ar = Ph, ArF; R = Me, Tol; L2 = bpy, tmeda), which immediately undergo methyl aroate exchange with PdIIMeR(L2) to give PdII(O2CAr)R(L2) and PdIV(O2CAr)Me2R(L2), where all products except for PdIV(O2CAr)Me2- Tol(tmeda) were detected by 1H NMR spectroscopy. On raising the temperature, the PdIVMe3 complexes reductively eliminate Me-Me, and the PdIVMe2Tol complexes eliminate Me- Me and Tol-Me. The resultant Pd(II) complexes PdII(O2CAr)R(L2) react with (ArCO2)2 at higher temperatures to form PdII(O2CAr)2(L2) and R-O2CAr (R = Me, Tol), except for PdII(O2- CAr)Tol(tmeda), which forms PdII(O2CAr)2(tmeda) and 4,4'-bitolyl. Each reaction step has been confirmed by the independent synthesis of intermediates PdII(O2CAr)2(L2) and PdII(O2- CAr)R(L2) (Ar =Ph, ArF; R=Me, Tol; L2 = bpy, tmeda) and PdIV(O2CR)Me2R(L2) (R = Ph, ArF; R= Me, Tol; L2 = bpy) by metathesis reactions of halogeno complexes with Ag[O2CAr], followed by temperature-dependent studies of both the decomposition of Pd(IV) complexes and reactions of Pd(II) complexes with (ArCO2)2. Attempts to prepare “PdIV(O2CAr)2MeR- (bpy)” in a similar manner (and thus in the absence of PdMeR(bpy) with which they undergo exchange reactions) were unsuccessful, but the complexes PdIVI2MeR(bpy) (R=) Me, Tol) that formed on reaction of diiodine with PdMeR(L2) were detected and found to reductively eliminate iodomethane. X-ray structural studies are reported for the square-planar palladium( II) complexes Pd(O2CPh)2(bpy), Pd(O2CAr)2(tmeda) (Ar = Ph, ArF), and Pd(O2CPh)-
|Journal or Publication Title:||Organometallics|
|Page Range:||pp. 1122-1131|
|Identification Number - DOI:||10.1021/om030644q|
|Additional Information:||The definitive version is available at http://www.sciencedirect.com|
|Date Deposited:||26 Sep 2007|
|Last Modified:||18 Nov 2014 03:21|
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