Cyclodextrin-functionalized graphene nanosheets, and their host-guest polymer nanohybrids

被引:26
|
作者
Xu, Li Qun [1 ]
Yee, Yon Kiat [1 ]
Neoh, Koon-Gee [1 ]
Kang, En-Tang [1 ]
Fu, Guo Dong [2 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 119260, Singapore
[2] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Jiangsu, Peoples R China
关键词
Reduced graphene oxide; Nitrene; Host-guest interaction; WALLED CARBON NANOTUBES; SOLVOTHERMAL REDUCTION; EXFOLIATED GRAPHENE; BETA-CYCLODEXTRIN; NITRENE CHEMISTRY; OXIDE NANOSHEETS; GRAPHITE OXIDE; FACILE; FILMS; WATER;
D O I
10.1016/j.polymer.2013.02.043
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
beta-Cyclodextrin (CD)-functionalized (grafted) reduced graphene oxide (RGO-g-CD) nanosheets were prepared via solution-based synthesis in one-pot, involving the simultaneous solvothermal reduction of graphene oxide (GO) and nitrene addition of azido-labeled CD to RGO. Being water soluble, the grafted CD imparted good dispersibility and stability to the RGO-g-CD nanosheets in water. The RGO-g-CD nanosheets were further functionalized with poly(N-isopropylacrylamide-co-vinylferrocene(II)) (PNI-PAM-Fc) and ferrocene-modified hyperbranched polyglycerol (HPG-Fc) via host-guest inclusion complexation of CD and ferrocene (Fc) moieties to form RGO-g-CD/Fc-PNIPAM and RGO-g-CD/Fc-HPG nanohybrids, respectively. Both RGO-g-CD/Fc-PNIPAM and RGO-g-CD/Fc-HPG nanohybrids were dispersible and stable in a wider range of solvents than the RGO-g-CD precursor nanosheets. Due to the thermoresponsive behavior of the attached PNIPAM moieties, the RGO-g-CD/Fc-PNIPAM exhibited reversible dispersibility in aqueous solution at a lower critical solution temperature (LCST) of 28 degrees C and thus could potentially be developed into thermoresponsive nanodevices. The RGO-g-CD/Fc-HPG nanohybrids exhibited low cytotoxicity towards 3T3 fibroblasts in 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) cell viability assay. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2264 / 2271
页数:8
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