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国家自然科学基金(50773038)

作品数:5 被引量:17H指数:2
相关作者:高超周立尹辉军徐伟箭徐宇虹更多>>
相关机构:浙江大学上海交通大学湖南大学更多>>
发文基金:国家自然科学基金国家重点基础研究发展计划中国博士后科学基金更多>>
相关领域:理学医药卫生一般工业技术更多>>

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Click chemistry approach to functionalize two-dimensional macromolecules of graphene oxide nanosheets被引量:6
2010年
A facile "click chemistry" approach to functionalize 2D macromolecules of graphene oxide nanosheets with poly(ethylene glycol) of different molecular weights,polystyrene,palmitic acid and various amino acids was presented.FTIR,TGA,Raman spectroscopy,XPS,XRD,TEM,AFM and SEM were utilized to characterize the products.High degree of functionalization was achieved on the flat surfaces of graphene oxide,affording polymer-grafted 2D brushes and amino acids-immobilized nanosheets,which show improved solubility in organic solvents.The click chemistry strategy reported herein provides a facile and general method for functionalization of graphene oxide with macromolecules and desired biomolecules.
Liang KouHongkun HeChao Gao
关键词:PEG
Functionalization of carbon nanotubes and other nanocarbons by azide chemistry被引量:2
2010年
Following the conventional carbon allotropes of diamond and graphite,fullerene,carbon nanotubes(CNTs) and graphene as 0D,1D and 2D graphitic macromolecules have been discovered recently in succession,declaring the unlimited potential of carbon-based nanomaterials and nanotechnology.Although CNTs exhibit significant potential applications in advanced materials and other fields due to their extraordinary mechanical strength and electrical/thermal conductivity properties,their low solubility,poor wettability and bad dispersibility in common solvents and solid matrices have limited their processing and applications.Thus,the attempt to achieve wettable/processable CNTs by functionalization has attracted increasing attention in both scientific and industrial communities.In recent years,azide chemistry has been demonstrated as a powerful means to covalently modify CNTs.It consists of two major approaches:click chemistry and nitrene chemistry,which both involve the usage of various azide compounds.The former one is based on highly reactive and stereospecifical Cu(I) catalyzed azide-alkyne cycloaddition reaction;the latter one is based on the electrophilic attack to unsaturated bonds of CNTs with nitrenes as reactive intermediates formed from thermolysis or photolysis of azides.In this mini-review paper,the azide chemistry to functionalize CNTs is highlighted and the corresponding functionalization routes to build CNT-based complex structures are also discussed.Besides,covalent functionalizations of other graphitic nanomaterials such as fullerence and graphene,via azide chemistry,are commented briefly.
Jin HanChao Gao
关键词:FUNCTIONALIZATIONFULLERENE
点击化学法快速合成氨基酸功能化的环糊精聚轮烷被引量:2
2010年
通过叠氮-炔环加成点击反应制备了各种氨基酸功能化的生物相容性β-环糊精封端的α-环糊精聚轮烷.利用FTIR和氢核磁共振谱对产物的结构进行了表征.结果证明对于空间位阻较小的分子,点击反应能够在很短的时间(几分钟)内达到近100%的转化率.点击化学为功能化聚轮烷的制备提供了快速有效的新途径.
吴佳燕高超
关键词:环糊精点击化学功能化
新型多杂臂超支化聚缩水甘油的简易合成及自组装行为被引量:6
2011年
通过简单的三步反应制备一种新型的两亲性多杂臂超支化聚缩水甘油(HPG-h-arm).先利用阴离子开环聚合制备HPG核,再利用1,3-二环己基碳化二亚胺(DCC)缩合反应,将疏水性的棕榈酸(PA)链和活性溴接枝到HPG上,最后利用原子转移自由基聚合反应(ATRP)将亲水性的聚N,N-二甲氨基甲基丙烯酸乙酯)(PDMAEMA)链接枝到HPG表面.用红外光谱(FTIR)、核磁共振谱(1HNMR)和凝胶渗透色谱(GPC)表征了HPG-h-arm.利用动态光散射仪(DLS)、透射电子显微镜(TEM)和原子力显微镜(AFM)研究了HPG-h-arm在不同溶剂中的自组装行为和形貌.结果表明,HPG-h-arm在不同的溶剂中可以自组装得到不同尺寸的球状胶束.
周立尹辉军高超徐伟箭
关键词:超支化聚合物自组装
靶向性多肽修饰荧光功能化碳纳米管的制备及靶向肿瘤细胞的初步研究被引量:2
2009年
以羟基化多壁碳纳米管(MWNT-OH)为引发剂,通过原位负离子开环聚合制备了生物相容性多羟基超支化聚缩水甘油接枝的碳纳米管(MWNT-HPG),利用酯化反应将荧光分子罗丹明6B标记于聚合物上,然后聚合物上的羟基和丁二酸酐反应将其转化为羧基.用TGA、FTIR、TEM、SEM等手段对产物进行了表征.用靶向表皮生长因子受体(EGFR)的小分子多肽D4修饰了所得的荧光功能化碳纳米管,并将其做为受体介导靶向肿瘤细胞的纳米载体,通过噻唑蓝(MTT)比色法评价功能化碳纳米管作为载体的安全性.用荧光显微镜观察其与人肺腺癌细胞SPCAI细胞的结合状态.结果证明了其有希望成为受体介导靶向肿瘤系统的纳米载体.
王雪周立高超徐宇虹
关键词:功能化碳纳米管荧光标记肿瘤靶向
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