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基于胍衍生物的高选择性和高灵敏度荧光关闭型 Cu 探针。

A Highly Selective and Sensitive Fluorescent Turn-Off Probe for Cu Based on a Guanidine Derivative.

机构信息

Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China.

出版信息

Molecules. 2017 Oct 16;22(10):1741. doi: 10.3390/molecules22101741.

DOI:10.3390/molecules22101741
PMID:29035343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6151758/
Abstract

A new highly selective and sensitive fluorescent probe for Cu, --butyl-4-(1'-cyclooctene-1',3',6'-triazole)-1,8-naphthalimide (), was synthesized and evaluated. The structure of compound was characterized via IR, ¹H-NMR, C-NMR and HRMS. The fluorescent probe was quenched by Cu with a 1:1 binding ratio and behaved as a "turn-off" sensor. An efficient and sensitive spectrofluorometric method was developed for detecting and estimating trace levels of Cu in EtOH/H₂O. The ligand exhibited excitation and emission maxima at 447 and 518 nm, respectively. The equilibrium binding constant of the ligand with Cu was 1.57 × 10⁴ M, as calculated using the Stern.

摘要

一种新的高选择性和高灵敏度的荧光探针用于 Cu, - 丁基-4-(1'-环辛烯-1',3',6'-三氮唑)-1,8-萘二甲酰亚胺(),被合成和评估。化合物的结构通过 IR, ¹H-NMR,C-NMR 和 HRMS 进行了表征。荧光探针被 Cu 猝灭,具有 1:1 的结合比,并表现为“关闭”传感器。开发了一种用于检测和估计 EtOH/H₂O 中痕量 Cu 的高效灵敏的分光荧光法。配体的激发和发射最大值分别为 447nm 和 518nm。使用 Stern 计算,配体与 Cu 的平衡结合常数为 1.57×10⁴ M。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/3b856d501ebb/molecules-22-01741-sch003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/d4236d251d9f/molecules-22-01741-g011.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/3b856d501ebb/molecules-22-01741-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/13698818dab8/molecules-22-01741-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/4dbb431e7bdb/molecules-22-01741-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/7ad2c5a67985/molecules-22-01741-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/23de605cfc62/molecules-22-01741-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/d64dd927a89a/molecules-22-01741-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/077a0f8756e9/molecules-22-01741-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/3ec3ec6b3d76/molecules-22-01741-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/4445fd0613c3/molecules-22-01741-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/cf743d24a2fc/molecules-22-01741-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/9eb55f957ff9/molecules-22-01741-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/a47387f3ddc9/molecules-22-01741-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/779bdf54116c/molecules-22-01741-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/d4236d251d9f/molecules-22-01741-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/f960ceb1b015/molecules-22-01741-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cb/6151758/3b856d501ebb/molecules-22-01741-sch003.jpg

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