Dendritic Chelating Agents. 1. Cu(II) Binding to Ethylene Diamine Core Poly(amidoamine) Dendrimers in Aqueous Solutions

• Published in: Langmuir 2004-03, Vol.20 (7), p.2640-2651
• Main Authors: Diallo, Mamadou S, Christie, Simone, Swaminathan, Pirabalini, Balogh, Lajos, Shi, Xiangyang, Um, Wooyong, Papelis, Charalambos, Goddard, William A, Johnson, James H
• Format: Article
• Language: English
• Subjects: Chelating Agents - chemical synthesis; Chelating Agents - chemistry; Copper - chemistry; Ethylenediamines - chemistry; Hydrogen-Ion Concentration; Molecular Structure; Organometallic Compounds - chemical synthesis; Organometallic Compounds - chemistry; Polyamines - chemistry; Surface Properties; Water - chemistry
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la036108k

This paper describes an investigation of the uptake of Cu(II) by poly(amidoamine) (PAMAM) dendrimers with an ethylenediamine (EDA) core in aqueous solutions. We use bench scale measurements of proton and metal ion binding to assess the effects of (i) metal ion−dendrimer loading, (ii) dendrimer generation/terminal group chemistry, and (iii) solution pH on the extent of binding of Cu(II) in aqueous solutions of EDA core PAMAM dendrimers with primary amine, succinamic acid, glycidol, and acetamide terminal groups. We employ extended X-ray absorption fine structure (EXAFS) spectroscopy to probe the structures of Cu(II) complexes with Gx-NH2 EDA core PAMAM dendrimers in aqueous solutions at pH 7.0. The overall results of the proton and metal ion binding measurements suggest that the uptake of Cu(II) by EDA core PAMAM dendrimers involves both the dendrimer tertiary amine and terminal groups. However, the extents of protonation of these groups control the ability of the dendrimers to bind Cu(II). Analysis of the EXAFS spectra suggests that Cu(II) forms octahedral complexes involving the tertiary amine groups of Gx-NH2 EDA core PAMAM dendrimers at pH 7.0. The central Cu(II) metal ion of each of these complexes appears to be coordinated to 2−4 dendrimer tertiary amine groups located in the equatorial plane and 2 axial water molecules. Finally, we combine the results of our experiments with literature data to formulate and evaluate a phenomenological model of Cu(II) uptake by Gx-NH2 PAMAM dendrimers in aqueous solutions. At low metal ion−dendrimer loadings, the model provides a good fit of the measured extent of binding of Cu(II) in aqueous solutions of G4-NH2 and G5-NH2 PAMAM dendrimers at pH 7.0.