The unexpected reactivity of Zeise's anion in strong basic medium discloses new substitution patterns at the platinum centre |
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Authors: | Benedetti Michele Fanizzi Francesco P Maresca Luciana Natile Giovanni |
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Affiliation: | Dipartimento di Scienze e Tecnologie Biologiche ed Ambientali, Università degli Studi di Lecce, Via Monteroni, I-73100, Lecce, Italy. |
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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. |
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