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Tuning Reactivity of Platinum(II) Complexes

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4.3.4 Kinetics with NMR<br />

The substitution reaction <strong>of</strong> pzn as a chloride, i.e. [cis-{PtCl(NH3)2}2-μ-pzn}] +2 with<br />

excess TU (6 equiv.), was studied by 1H and 195Pt NMR spectroscopy. The 1H and 195Pt<br />

NMR spectra <strong>of</strong> the substitution reaction <strong>of</strong> the [{cis–PtCl(NH3)2}2–μ–pzn](ClO4)2 with<br />

TU are presented in Figures 4.8 and 4.9, respectively. The NMR spectral arrays were also<br />

used to determine the rate <strong>of</strong> dechelation <strong>of</strong> the pyrazine ligand as shown in figure 4.10.<br />

Figure 4.8: 1 H NMR spectra in D2O <strong>of</strong> the aromatic region <strong>of</strong> 0.022mM [{cis-PtCl (NH3)2}2-<br />

µ-pzn] +2 reaction with TU at 30°C showing the production <strong>of</strong> the major<br />

degradation product free pyrazine (L) at δ 8.68 ppm and the starting complex<br />

(A) at δ = 9.04 ppm. These spectra are indicative <strong>of</strong> the formation <strong>of</strong> other<br />

minor transient intermediate products.<br />

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