Water-soluble PEGylated silicon nanoparticles and their assembly into swellable nanoparticle aggregates

被引:9
|
作者
Xu, Zejing [1 ]
Li, Yejia [1 ]
Zhang, Boyu [1 ]
Purkait, Tapas [1 ]
Alb, Alina [2 ]
Mitchell, Brian S. [3 ]
Grayson, Scott M. [1 ]
Fink, Mark J. [1 ]
机构
[1] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
[2] Tulane Univ, Dept Phys & Engn Phys, New Orleans, LA 70118 USA
[3] Tulane Univ, Dept Chem & Biomol Engn, New Orleans, LA 70118 USA
基金
美国国家科学基金会;
关键词
Silicon; Nanoparticles; PEG; Nanohydrogel; Nanocolloids; QUANTUM DOTS; POROUS SILICON; MECHANOCHEMICAL SYNTHESIS; FUNCTIONALIZED SILICON; CLICK CHEMISTRY; DRUG-DELIVERY; SURFACE; SI; NANOCRYSTALS; FLUORESCENT;
D O I
10.1007/s11051-015-2869-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Water-soluble silicon nanoparticles were synthesized by grafting PEG polymers onto functionalized silicon nanoparticles with distal alkyne or azide moieties. The surface-functionalized silicon nanoparticles were produced in one step from the reactive high-energy ball milling (RHEBM) of silicon wafers with a mixture of either 5-chloro-1-pentyne in 1-pentyne or 1,7 octadiyne in 1-hexyne to afford air and water-stable chloroalkyl or alkynyl-terminated nanoparticles, respectively. Nanoparticles with the xchloroalkyl substituents were easily converted to xazidoalkyl groups through the reaction of the Si nanoparticles with sodium azide in DMF. The azido-terminated nanoparticles were then grafted with mono-alkynyl-PEG polymers using a copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction to afford core-shell silicon nanoparticles with a covalently attached PEG shell. Covalently linked Si nanoparticle clusters were synthesized via the CuAAC "click'' reaction of functional Si NPs with alpha,omega-functional PEG polymers of various lengths. Dynamic light scattering studies show that the flexible globular nanoparticle aggregates undergo a solvent-dependent change in volume (ethanol>dichloromethane>toluene) similar in behavior to hydrogel nanocomposites.
引用
收藏
页数:16
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