Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12888
Title: Kinetics, mechanism and density functional theory calculations on base hydrolysis of α-amino acid esters catalyzed by [Pd(AEMP)(H<inf>2</inf>O)<inf>2</inf>]<sup>2+</sup> (AEMP = 2-(2-aminoethyl)-1-methylpyrrolidine)
Authors: Shoukry M.
Shehata, Mohamed
Ragab M.
Ćorćić D.
Puchta, Ralph
van Eldik R.
Journal: Reaction Kinetics, Mechanisms and Catalysis
Issue Date: 1-Apr-2020
Abstract: © 2020, Akadémiai Kiadó, Budapest, Hungary. Abstract: Pd(AEMP)Cl2 (AEMP = 2-(2-aminoethyl)-1-methylpyrrolidine) was synthesized and characterized by spectral and thermal measurements.[Pd(AEMP)(H2O)2]2+ reacts with amino acid esters (L) to form mixed ligand [Pd(AEMP)L]2+ complexes. The kinetics of the base hydrolysis of [Pd(AEMP)L]2+ was studied by a pH-stat technique and the corresponding rate constants are reported. The coordinated glycine methyl ester is hydrolyzed efficiently, whereas the coordinated methionine- and histidine- methyl esters undergo hydrolysis with a much lower catalytic activity. The catalytic effect is controlled by the mode of coordination of the ester to the Pd(II) complex. Possible mechanisms for these reactions are considered. Activation parameters were determined experimentally for the hydrolysis of the coordinated glycine methyl ester. DFT calculations (B3LYP/def2svp) were applied to gain further insight into the possible mechanism of the base hydrolysis of the amino acid esters. The calculations are discussed in reference to the reported experimental data. Graphic abstract: [Figure not available: see fulltext.]
URI: https://scidar.kg.ac.rs/handle/123456789/12888
Type: Article
DOI: 10.1007/s11144-020-01734-7
ISSN: 18785190
SCOPUS: 85079446029
Appears in Collections:University Library, Kragujevac
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