Poly(amidoamine) dendrimers: A new class of high capacity chelating agents for Cu(II) ions

被引:167
作者
Diallo, MS
Balogh, L
Shafagati, A
Johnson, JH
Goddard, WA
Tomalia, DA
机构
[1] Howard Univ, Dept Civil Engn, Washington, DC 20059 USA
[2] Howard Univ, Dept Chem, Washington, DC 20059 USA
[3] CALTECH, Beckman Inst 139 74, Mat & Proc Simulat Ctr, Pasadena, CA 91125 USA
[4] Univ Michigan, Sch Med, Ctr Biol Nanotechnol, Ann Arbor, MI 48109 USA
[5] Michigan Mol Inst, ARL MMI Dendrit Polymers Ctr Excellence, Midland, MI 48640 USA
关键词
D O I
10.1021/es980521a
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This communication describes preliminary results of an experimental investigation of the binding of Cu(II) ions to poly(amidoamine) (PAMAM) dendrimers in aqueous solutions. Dendrimers are highly branched polymers with controlled composition and architecture consisting of three structural components: a core, interior branch cells, and terminal branch cells. PAMAM dendrimers possess functional nitrogen and amide groups arranged in regular "branched upon branched" patterns which are displayed in geometrically progressive numbers as a function of generation level. Terminal groups of PAMAM dendrimers may be any organic substituent such as primary amines, carboxylic groups, etc. In aqueous solutions, PAMAM dendrimers can serve as high capacity nanoscale containers for toxic metal ions such as Cu(II). Compared to traditional chelating agents (e.g., triethylene tetramine) and macrocyles (e.g., cyclams) with nitrogen donors, which can typically bind only one Cu(II) ion per molecule, a generation eight (G8) PAMAM dendrimer can bind up 153 +/- 20 Cu(II) ions per molecule. This clearly illustrates a distinct advantage of dendrimers over traditional chelating agents and macrocycles; that is the covalent attachment of nitrogen ligands to conformationally flexible PAMAM chains enclosed within a nanoscopic structure results in a substantial increase in binding capacity.
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页码:820 / 824
页数:5
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