
Journal of Organometallic Chemistry p. 399 - 407 (1990)
Update date:2022-08-17
Topics:
Byers, Peter K.
Canty, Allan J.
Traill, Peter R.
Watson, Andrew A.
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 palldium metal are also formed, and are attributed to decomposition of PdIEt(bpy) via β-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
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(1984)