Noncovalent interaction of polyethylene glycol with copper complex of ethylenediaminetetraacetic acid and its application in constructing inorganic nanomaterials

• Published in: Dalton transactions : an international journal of inorganic chemistry 2011-01, Vol.40 (39), p.10117-10124
• Main Authors: Pan, Shu Zhen, Song, Le Xin, Chen, Jie, Du, Fang Yun, Yang, Jing, Xia, Juan
• Format: Article
• Language: English
• Subjects: ACETIC ACID; Adducts; CHEMICAL PROPERTIES; Coordination Complexes - chemistry; Coordination compounds; Copper; Copper - chemistry; COPPER COMPOUNDS; Crystals; Edetic Acid - chemistry; ETHYLENE; ETHYLENE GLYCOL; ETHYLENEDIAMINE; ETHYLENEDIAMINE TETRAACETIC ACID; Ethylenediaminetetraacetic acids; Nanomaterials; Nanostructures - chemistry; Nanostructures - ultrastructure; ORGANIC COMPOUNDS; POLYETHYLENE; Polyethylene glycol; Polyethylene Glycols - chemistry; Stacking; Temperature
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/c1dt11090j

In this study, we try to answer a fundamental question: what is the consequence of the noncovalent interaction between a polymer and a coordination compound? Here, polyethylene glycol (PEG-4000, PEG-b) and copper complex of ethylenediaminetetraacetic acid (H(2)CuY) were employed to solve this problem. A novel adduct (CEP) between H(2)CuY and PEG-b was prepared. Our results indicated several interesting findings. First, the introduction of H(2)CuY had no effect on the stacking structure of PEG-b but led to a large change in surface structure of the polymer. Second, there was a significant difference (117 K) in the maximum degradation temperature between the PEG and the CEP, suggesting that the noncovalent interaction can drastically improve the thermal stability of the PEG. Third, sintering experiments showed that H(2)CuY and CEP produced completely different decomposition products. The former formed Cu crystals in nitrogen and CuO in air, but the latter generated Cu and CuCl crystals with good crystallinity, respectively. Finally, three independent measurements: viscosity, conductivity and nuclear magnetic resonance in solution, provided useful information and insights from both sides of the noncovalent interaction. Probable interaction mechanisms and interaction sites were proposed. We consider that the current research could create the foundation for a new understanding of how the noncovalent adduct interaction between a metallic complex and a polymer relates to the change in physical and chemical properties of the adducted components.