Article,

Stereospecific Intramolecular S$\rightarrow$Pt Transmethylation from 8-(Methylthio)quinoline to Coordinated PtMe2: Formation of syn-[fac-PtIVMe3(m-8-quinolinethiolato)]2 with Stacked Quinoline Rings

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Organometallics, 24 (5): 794--796 (2005)
DOI: 10.1021/om049247l

Abstract

S to Pt(II) transmethylation was obsd. on reacting [PtMe2(m-SMe2)]2 or [PtMe2(m-SEt2)]2 with 8-(methylthio)quinoline (mtq) for extended periods of time or on heating of the isolable intermediate PtMe2(mtq). The final product, syn-[fac-PtMe3(m-qt)]2 (qt- = 8-quinolinethiolato), exhibits two quinoline rings in a nearly stacked arrangement. This internal redox reaction involving organometallic Pt constitutes a variant of the known Pt complex induced S-demethylation and proceeds in a stereospecific manner, as indicated by CD3 labeling expts. [on SciFinder(R)]

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