Abstract
The reaction of tetrameric [PtMe3(OTf)]4 (OTf = triflate = CF3SO3–) with TMEDA (N,N,N,N-tetramethylethylenediamine) gave the monomeric compound PtMe3(OTf)·TMEDA in quantitative yield. The non-planar TMEDA ligand contains two different sorts of methyl groups in PtMe3(OTf)·TMEDA, and thus offers a second and independent set of NMR parameters in addition to the commonly used signals of the Me3Pt ...
Abstract
The reaction of tetrameric [PtMe3(OTf)]4 (OTf = triflate = CF3SO3–) with TMEDA (N,N,N,N-tetramethylethylenediamine) gave the monomeric compound PtMe3(OTf)·TMEDA in quantitative yield. The non-planar TMEDA ligand contains two different sorts of methyl groups in PtMe3(OTf)·TMEDA, and thus offers a second and independent set of NMR parameters in addition to the commonly used signals of the Me3Pt unit. The additional information derived from these NMR data provides detailed insight into the mechanistic picture of chelating phenomena at PtIV. At low temperature the twisting of the ethylene bridge of the TMEDA ligand can be observed; at room temperature an intramolecular two-step ligand exchange takes place. Evidence for an equilibrium involving a TMEDA chelate as well as a 2-O3SCF3 chelate has been found. Dependent on the applied temperature, two types of ligand exchange motions can be distinguished by dynamic NMR spectroscopy because of their different activation parameters. These motions have been identified as the two essential steps in the so-called windscreen-wiper process that has been invoked for exchange phenomena in Me3Pt complexes previously. Moreover, the data indicate the crucial role of a 2-triflate in this process in PtMe3(OTf)·TMEDA.
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