罗丹明6G
共聚物
光化学
链式转移
化学
部分
聚(N-异丙基丙烯酰胺)
罗丹明
聚合
荧光
高分子化学
水溶液
费斯特共振能量转移
光致发光
材料科学
自由基聚合
有机化学
分子
聚合物
物理
量子力学
光电子学
作者
Fantao Kong,Mengqi Lin,Teng Qiu
出处
期刊:Polymer
[Elsevier]
日期:2018-08-01
卷期号:151: 117-124
被引量:14
标识
DOI:10.1016/j.polymer.2018.07.068
摘要
We have synthesized a multi-functional copolymer poly(N-isopropylacrylamide) (PNIPAM) containing rhodamine 6G and 1,8-naphthalimide moieties via reversible addition-fragmentation chain transfer (RAFT) radical polymerization. In a neutral condition, only an emission band with a peak at 520 nm is observed in the copolymer, which originates from 1,8-naphthalimide. The 520-nm photoluminescence (PL) intensity is markedly increased with decreasing the pH value of Britton-Robinson buffers, but changed instinctively by the concentration of Fe3+. The spirolactam ring-opening of the rhodamine 6G moiety is responsible for the PL changes of the copolymer in acidic conditions and Fe3+ aqueous solution, correspondingly, the 555-nm PL band of rhodamine 6G can be found for excitation at 400 nm. The PL intensity at 555 nm relative to that at 520 nm (I555/I520) is dependent on the resonance energy transfer from 1,8-naphthalimide to rhodamine 6G, which can be controlled by the chain conformations of the themoresponsive copolymer. The good linear relationships between the PL changes and the detection objects mean that the copolymer can be served as ratiometric chemosensors to probe pH, Fe3+ ions and temperature.
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