The unexpected reactivity of Zeise's anion in strong basic medium discloses new substitution patterns at the platinum centre

Chem Commun (Camb). 2006 Mar 14:(10):1118-20. doi: 10.1039/b516818j. Epub 2006 Jan 25.

Abstract

Zeise's anion in strongly basic hydroxylated solvents undergoes unprecedented nucleophilic addition of OR- (R = H, Me, Et) to the eta2-ethene giving trans-[PtCl2(eta1-C2H4OR)(OR)]2- which readily reacts with bidentate nitrogen donors N-N to give Cl- and OR- substitution and formation of [PtCl(CH2CH2OR)(N-N)]. Protonolysis of this stable organometallic species offers a versatile route to cationic [PtCl(eta2-C2H4)(N-N)]+ complexes.