A trans influence and π-conjugation effects on ligand substitution reactions of Pt(II) complexes with tridentate pendant N/S-donor ligands
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Date
2018
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College of Natural and Applied Sciences (CoNAS) of the University of Dar es Salaam (UDSM)
Abstract
The rate of displacement of the chloride ligands by three neutral nucleophiles (Nu) of different steric demands, namely thiourea (TU), N,N’-dimethylthiourea (DMTU) and N,N,N,’Ntetramethylthiourea (TMTU) in the complexes viz; [Pt(II)(bis(2-pyridylmethyl)amine)Cl]ClO4, (Pt1), [Pt(II){N-(2-pyridinylmethyl)-8-quinolinamine}Cl]Cl, (Pt2), [Pt(II)(bis(2-pyridylmethyl)sulfide)Cl]Cl, (Pt3) and [Pt(II){8-((2-pyridylmethyl)thiol)quinoline}Cl]Cl, (Pt4) was studied under pseudo first-order conditions as a function of concentration and temperature using a stopped-flow technique and UV-Visible spectrophotometry. The observed pseudo first order rate constants for substitution reactions obeyed the simple rate law kobs =[Nu] k2. The results have shown that the chloro ligand in Pt(N^S^N) complexes is more labile by two orders of magnitude than Pt(N^N^N) complexes due to the high trans labilizing effect brought by the S donor atom. The quinoline based Pt(II) complexes (Pt2 and Pt4) have been found to be slow than their pyridine counterparts Pt1 and Pt3 due to poor π-acceptor ability of quinoline. Second-order kinetics and large negative activation entropies support an associative mode of activation.
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Keywords
Substitution, nucleophiles, pseudo first-order, associative, entropy
Citation
GA Kinunda - Tanzania Journal of Science, 2018