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Articles

Thermal stability of Pd(1,4-bis(2-hydroxyethyl)piperazine)Cl2 and its role in the catalysis of base hydrolysis of α-amino acid esters

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Pages 3272-3281 | Received 27 Feb 2015, Accepted 06 May 2015, Published online: 06 Jul 2015
 

Abstract

Pd(BHEP)Cl2 was synthesized and characterized (BHEP = 1,4-bis(2-hydroxyethyl)piperazine). The complex decomposes in two steps, leaving a residue of palladium metal. Amino acid ester (L) reacts with [Pd(BHEP)(H2O)2]2+ (BHEP = 1,4-bis(2-hydroxyethyl)piperazine), giving mixed-ligand complexes, [Pd(BHEP)L]2+. The kinetics of hydrolysis of [Pd(BHEP)L]2+ have been studied by pH-stat technique, and rate constants were obtained. Rate acceleration observed for glycine methyl ester is high. The effect with methionine methyl ester is much less marked, as the mixed-ligand complexes with these ligands do not involve alkoxycarbonyl donors. Possible mechanisms for these reactions are considered.

Graphical abstract

The thermal stability of Pd(BHEP)Cl2 complex was investigated. The role of the complex in the catalysis of amino acid esters was studied.

Disclosure statement

No potential conflict of interest was reported by the authors.

Notes

Dedicated to Prof. Rudi van Eldik on the occasion of his 70th birthday.

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