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多重响应性大分子荧光探针的合成与性能 被引量:1

Synthesis and properties of multiple responsive macromolecule fluorescent probe
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摘要 由偶氮二异丁腈(AIBN)引发N-异丙基丙烯酰胺(NIPAM)和N-丙烯酰氧基丁二酰亚胺(NA-SI)及3-丙烯酰氧基荧光素(Ac-Flu)进行三元共聚,得到P(Flu-co-NASI-co-NIPAM)三元共聚物。进而在碱性条件下使荧光小分子9-氨基吖啶(9AA)与共聚物中的丁二酰亚胺酯基反应,制得了温度和pH值多重响应性大分子荧光探针P(Flu-co-9AA-co-NIPAM)。利用FT-IR、1 H NMR、GPC、UV-Vis等对大分子荧光探针的结构及分子量进行表征,并用荧光光谱测定其水溶液的荧光强度。结果表明,当体系温度和pH值变化时,荧光颜色均可发生可逆转变,T<33℃(LCST)或pH值=8.9时呈现黄绿色,当T≥33℃或pH值=3.1时呈蓝色,该大分子荧光探针具有多重响应性。 P(Flu-co-NASI-co-NIPAM) copolymer was prepared by free radical copolymerization of N-isopropy- lacrylamide (NIPAM), 3-acryloxy fluorescein (Ac-Flu) and N-acryloxysuccinimide (NASI) using azodiisobuty ronitrile (AIBN) as initiator. Then, 9-aminoaeridine was employed as chromophore to successfully modify the P(Flu-co-NASI-co-NIPAM) to form thermo-pH multiple responsible macromolecule fluorescent probe, P(Flu co-9AA-eo-NIPAM) at alkaline condition. Its chemical structure and number-average molecular weight were characterized by FT-IR, 1H NMR, GPC and UV-Vis. The fluorescence intensity was measured using fluores- cence spectra. Results revealed that when T〈33 ℃ (LCST) or pH=8.9, a yellowgreen fluorescence emission of copolymer is observed. Upon adjusting to T≥33℃ or pH=3.1, the emission is blue. Moreover, the emis- sion transition of copolymer showed reversibly and efficiently by changing temperature and pH.
出处 《功能材料》 EI CAS CSCD 北大核心 2013年第12期1796-1799,共4页 Journal of Functional Materials
基金 国家自然科学基金资助项目(51173072)
关键词 N-异丙基丙烯酰胺 荧光素 9-氨基吖啶 大分子荧光探针 可逆转变 NIPAM fluorescein 9-aminoaeridine macromolecule fluorescent probe reversibly transition
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