Organopalladium ArPdL(2)I (L = tertiary phosphine) complexes (1) can b
e synthesized in one step from the precursors Pd-2(dba)(3) . C6H6 (2)
(dba = t,t-dibenzylideneacetone) and (eta(3)-allyl)PdCp (3) (Cp = eta(
5)-cyclopentadienide). Two advantages over previous synthetic methods
are that-this route requires only stoichiometric amounts of phosphine
and that the desired complexes are easily isolated fi om reaction bypr
oducts. The scope and generality of these reactions are investigated,
and the synthesis of a number of new organic- and water-soluble comple
xes utilizing this methodology is discussed. Improved syntheses of wat
er-soluble ligands P(C6H5)(2)(4-SO3KC6H4) (5) and As(C6H5)(2)(4-SO3KC6
H4) (6) are presented as well.