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A versatile method for the preparation of end-functional polymers onto SiO2 nanoparticles by a combination of surface-initiated ATRP and Huisgen [3+2] cycloaddition
被引:36
作者:
Chen, J. C.
[1
]
Luo, W. Q.
[1
]
Wang, H. D.
[1
]
Xiang, J. M.
[1
]
Jin, H. F.
[1
]
Chen, F.
[2
]
Cai, Z. W.
[2
]
机构:
[1] Ankang Univ, Dept Chem & Chem Engn, Ankang 725000, Peoples R China
[2] Ankang Univ, Dept Agr & Life Sci, Ankang 725000, Peoples R China
关键词:
Surface modification;
Atom-transfer radical polymerization (ATRP);
Cu-catalyzed Huisgen [3+2] cycloaddition;
Chain-end functionalization;
TRANSFER RADICAL POLYMERIZATION;
CLICK CHEMISTRY;
SILICA;
PHASE;
BRUSHES;
GRAFT;
CONSTRUCTION;
COPOLYMERS;
BLOCK;
D O I:
10.1016/j.apsusc.2009.10.093
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A versatile method was developed for the chain-end functionalization of the grafted polymer chains for surface modi. cation of nanoparticles with functionalized groups through a combination of surface-initiated atom-transfer radical polymerization (ATRP) and Huisgen [3 + 2] cycloaddition. First, the surface of SiO2 nanoparticles was modified with poly(methyl methacrylate) (PMMA) brushes via the "grafting from'' approach. The terminal bromides of PMMA-grafted SiO2 nanoparticles were then transformed into an azide function by nucleophilic substitution. These azido-terminated PMMA brushes on the nanoparticle surface were reacted with alkyne-terminated functional end group via Huisgen [3 + 2] cycloaddition. FTIR and H-1 NMR spectra indicated quantitative transformation of the chain ends of PMMA brushes onto SiO2 nanoparticles into the desired functional group. And, the dispersibility of the end-functional polymer-grafted SiO2 nanoparticles was investigated with a transmission electron microscope (TEM). (C) 2009 Elsevier B. V. All rights reserved.
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页码:2490 / 2495
页数:6
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