کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5009361 | 1462044 | 2017 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A water-soluble, cationic bis-porphyrin exhibiting a more sensitive fluorescent response to Cu2+ relative to its monomeric counterpart
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: A water-soluble, cationic bis-porphyrin exhibiting a more sensitive fluorescent response to Cu2+ relative to its monomeric counterpart A water-soluble, cationic bis-porphyrin exhibiting a more sensitive fluorescent response to Cu2+ relative to its monomeric counterpart](/preview/png/5009361.png)
چکیده انگلیسی
A water-soluble, cationic bis-porphyrin (Bis-TMPipEOPP) was synthesized, characterized, and its optical properties were investigated. Its fluorescence was found to be specifically quenched by paramagnetic Cu2+ ions via a static quenching mechanism. Based on these findings, an organic solvent-free sensing platform was developed for the “turn-off” detection of Cu2+. Such a platform could achieve sensitive Cu2+ quantitation at a detection limit of 8.8Â nM. Compared to its monomeric counterpart TMPipEOPP, Bis-TMPipEOPP exhibited a higher tendency to self-aggregate due to the synergy between the two porphine rings. This characteristics conferred the proposed Bis-TMPipEOPP-based Cu2+-sensing platform with a sensitive fluorescent response to low concentrations of Cu2+ in a linear detection range of between 10Â nM and 300Â nM. However, the TMPipEOPP-based method provided observable changes in the fluorescent signal only at Cu2+ concentrations >200Â nM. These results potentially offer a method for improving the performance of fluorescent-dye-based Cu2+ sensors.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Sensors and Actuators B: Chemical - Volume 247, August 2017, Pages 179-187
Journal: Sensors and Actuators B: Chemical - Volume 247, August 2017, Pages 179-187
نویسندگان
Ke-Ke Liu, Li-Na Zhang, Li-Na Zhu, Ran Zhang, Xiao-Zeng Li, De-Ming Kong,