## Abstract The kinetic course of the reactions of [Pt(dipic~tr~)Cl]^−^ (where H~2~dipic = pyridine‐2,6‐dicarboxylic acid; bonded in tridentate mode) with glycine, β‐alanine, and L‐histidine was followed at 25°C in aqueous medium at pH 3.00–10.73 at I = 0.5 mol dm^−3^ (LiClO~4~) spectrophotometrica
Kinetics and mechanism of the reactions of platinum(II)-dipicolinate and platinum(II)-glycylglycine with oxalate ion
✍ Scribed by Sukalpa Dey; Pradyot Banerjee
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 105 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The kinetics of the reactions of [Pt(dipic)(H~2~O)] and [Pt(digly)(H~2~O)] (where H~2~dipic = pyridine‐2,6‐dicarboxylic acid and H~2~digly = glycylglycine) with oxalate ion were studied at 25°C in aqueous medium by UV–vis spectroscopy at I = 0.1 mol dm^−3^ over an wide range of pH. A probable associative pathway may involve a five‐coordinate intermediate leading to the formation of an unidentate oxalate species, which converts to bidentate chelate in subsequent fast steps. The products are isolated and characterized by CHN analysis, IR, and ^1^H NMR spectra. The kinetic data from pH variation experiments are fitted by a computer program to a sequence of reactions and the different rate constants are evaluated. © 2003 Wiley Periodicals, Inc. Int J Chem Kinet 35: 327–333, 2003
📜 SIMILAR VOLUMES
The rate constants for the protonation of "free" (that is, solvated) superoxide ions by water and ethanol are equal to 0.5-3.5 X lO-~M-l.s-' in DMF and AN at 20'. It has been found that the protonation rates for the ion pairs of 0; with the BudN+ cation are much slower than those for "free" 0,. It i