@article{epprod2954,
          volume = {390},
          number = {3},
           month = {["lib/utils:month\verb1_12954" not defined]},
          author = {PK Byers and AJ Canty and PR Traill and AA Watson},
            note = {The definitive version is available at http://www.sciencedirect.com},
           title = {Synthesis and decomposition of neutral palladium(IV)
complexes containing fac-PdMe2R groups, including reductive
elimination by etal-propenylpalladium(IV) complexes to form
eta3-propenylpalladium(II) species},
            year = {1990},
         journal = {Journal of Organometallic Chemistry},
           pages = {399--407},
             url = {http://eprints.utas.edu.au/2954/},
        abstract = {Oxidative addition of ethyl iodide to PdMe2(2,2?-bipyridyl) in (CD3)2CO gives the unstable ?PdIMe2Et(bpy)?, which undergoes reductive elimination to form PdIR(bpy) (R = Me, Et), ethane, and propane. Ethene and palladium metal are also formed, and are attributed to decomposition of PdIEt(bpy) via beta-elimination. Similar results are obtained with n-propyl iodide, although a palladium(IV) intermediate was not detected, but CH2=CHCH2X (X = Br, I) and PhCH=CHCH2Br give isolable complexes fac-PdXMe2(CH2CH=CHR)(L2) (R = H, Ph; L2 = bpy, phen). The propenyl complexes decompose at ambient temperature to form ethane, a trace of PdXMe(L2), and mixtures of [Pd(eta3-C3H5)(L2)]X and [Pd(eta3-C3H5)(L2)][Pd(eta3-C3H5)X2]; for fac-PdBrMe2(CH2CH=CH2)(bpy) the major palladium(II) product is [Pd(eta3-C3H5)(bpy)]Br.}
}