TY - JOUR
T1 - Synthesis, structures, and properties of a fluoranthene-based biphenol polymer as a fluorescent nano-thermometer
AU - Guo, Yanzhen
AU - Yu, Xue
AU - Xue, Wenwei
AU - Huang, Shuaishuai
AU - Dong, Jing
AU - Wei, Liuhe
AU - Maroncelli, Mark
AU - Li, Hongping
N1 - Funding Information:
This work was supported by funds from the National Natural Science Foundation of China (Nos. 21073167, J1210060), the China Scholarship Council [2011]3022, and the Innovative Research Grant for Undergraduate Students of Zhengzhou University (2012 and 2013). The authors appreciate Prof. Senxiang Cheng (Henan Academy of Sciences) for help identifying the structure of compound 4, Prof. Guangyue Bai (Henan Normal University) for her assistance in DLS measurements.
PY - 2014/3/15
Y1 - 2014/3/15
N2 - In this work, we explored a direct way of labeling poly(N-isopropylacrylamide) (PNIPAm) and developed a fluorescent thermometer with desired feature of aggregation-enhanced emission. A fluoranthene-based biphenol polymer, PNIPAm MAh-4 (PN4), consisting of N-isopropylacrylamide (NIPAm) and 4-(9-(2-(4-hydroxyphenyl)ethynyl)-7,10-diphenylfluoranthen-8-yl)-phenol (4) units as temperature-responsive and fluorescent signaling parts, respectively, was synthesized. The aqueous solution of PN4 exhibits weak fluorescence (FL) below 30. °C, whereas shows FL enhancement above 30. °C. The FL intensity increases with temperature monotonically until 50. °C, and the maximum FL intensity at 50. °C is about 7-fold higher than that at 15. °C. The FL enhancement is found to be associated with a heat-induced polymer chain conformation transition from hydrated coil to dehydrated globule. And the possible mechanisms for emission responses of PN4 against temperature, concentration and aggregation are suggested, respectively. The plausible mechanism of the sensitivity of the emission intensity to temperature or polymer state involves the deprotonation equilibrium and formation of the less fluorescent form of PN4. Meanwhile, the polymer possesses high reversibility of the FL response. Therefore the polymer PN4 is expected to have great potential as a fluorescent thermometer with high sensitivity and reversibility, and our work explores its utilities in molecular probes, biotechnology, multistimuli-responsive nanomaterials and smart polymer machines.
AB - In this work, we explored a direct way of labeling poly(N-isopropylacrylamide) (PNIPAm) and developed a fluorescent thermometer with desired feature of aggregation-enhanced emission. A fluoranthene-based biphenol polymer, PNIPAm MAh-4 (PN4), consisting of N-isopropylacrylamide (NIPAm) and 4-(9-(2-(4-hydroxyphenyl)ethynyl)-7,10-diphenylfluoranthen-8-yl)-phenol (4) units as temperature-responsive and fluorescent signaling parts, respectively, was synthesized. The aqueous solution of PN4 exhibits weak fluorescence (FL) below 30. °C, whereas shows FL enhancement above 30. °C. The FL intensity increases with temperature monotonically until 50. °C, and the maximum FL intensity at 50. °C is about 7-fold higher than that at 15. °C. The FL enhancement is found to be associated with a heat-induced polymer chain conformation transition from hydrated coil to dehydrated globule. And the possible mechanisms for emission responses of PN4 against temperature, concentration and aggregation are suggested, respectively. The plausible mechanism of the sensitivity of the emission intensity to temperature or polymer state involves the deprotonation equilibrium and formation of the less fluorescent form of PN4. Meanwhile, the polymer possesses high reversibility of the FL response. Therefore the polymer PN4 is expected to have great potential as a fluorescent thermometer with high sensitivity and reversibility, and our work explores its utilities in molecular probes, biotechnology, multistimuli-responsive nanomaterials and smart polymer machines.
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U2 - 10.1016/j.cej.2013.11.081
DO - 10.1016/j.cej.2013.11.081
M3 - Article
AN - SCOPUS:84890852840
SN - 1385-8947
VL - 240
SP - 319
EP - 330
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -