Abstract
Novel ABA-type dumbbell-like water-soluble copolymers [D230(EI)4, D400(EI)4, and D400(EI)8] were synthesized by introducing ethylenimine (EI) groups into both sides of polyoxypropylenediamines via a simple in situ ethylamination of polyoxypropylenediamine with 2-chloroethylamine hydrochloride. The structures of the resultant polymers were identified by Fourier transform infrared spectroscopy and 1H NMR. The percentages of primary, secondary, and tertiary amine present were determined by the potentiometric titration method after treatments with the appropriate chemicals of salicylaldehyde and acetic anhydride. The surface tension and solubilizing behavior of pyrene in the presence of these polymers in aqueous medium were also investigated, and the efficiency to reduce the surface tension and solubilizing behavior of pyrene depends on the attachments of EI to polymer backbone. The chelating properties of these polymers were examined quantitatively by ultraviolet–visible (UV–vis) spectroscopy in the presence of Cu2+ ions in aqueous solution, and continuous variation analysis revealed that the most stable complex is formed at the normality ratio of [N]/[Cu2+] = 3.0. UV–vis spectroscopy and transmission electron microscopy were used to evaluate the dumbbell-like water-soluble copolymer, D400(EI)8, as a stabilizer for preparing colloidal noble metal nanoparticles (Au and Pt) in aqueous solution. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1360–1370, 2003
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Polymer Science Part A: Polymer Chemistry
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.