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A dansyl-appended N-heterocycle for Cu2+ and S2- recognition via a displacement mode
被引:12
作者:
Wang, Xu
[1
]
Xia, Peng
[1
]
Huang, Xiaohuan
[1
]
机构:
[1] Hubei Normal Univ, Coll Chem & Chem Engn, Hubei Key Lab Pollutant Anal & Reuse Technol, Huangshi 435002, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Amide-containing heterocycle;
S2-;
recognition;
Displacement mode;
Cell imaging;
FLUORESCENT SWITCH;
HYDROGEN-SULFIDE;
SEQUENTIAL DETECTION;
AQUEOUS-SOLUTION;
SULFUR-COMPOUNDS;
COPPER(II) ION;
SCHIFF-BASE;
SENSOR;
ANION;
CHEMOSENSORS;
D O I:
10.1016/j.saa.2018.11.017
中图分类号:
O433 [光谱学];
学科分类号:
0703 ;
070302 ;
摘要:
A novel L-proline based heterocycle 3 of C-2 symmetry has been designed and synthesized for cation and anion recognition in aqueous solution. Ligand 3 shows a strong affinity to Cu2+ ion, and their interaction induces a remarkable fluorescence quenching in DMSO:H2O = 9:1 (HEPES buffer, 0.01 M, pH 7.4) among various metal ions. Both the in-situ generated and isolated 3-Cu2+ complex exhibit specific fluorescence recovery upon addition of S2-, even in the presence of S2O32-, L-histidine, and thiol-containing amino acids. For this dual functional switch, a combination of H-1 NMR titration, ESI mass and FT-IR spectra suggest that its sensing behavior is via a displacement mode. Sequential "on-off-on" fluorescence bio-imaging of the heterocycle 3 to Cu2+ and S2- was carried out in HeLa cells. (C) 2018 Elsevier B.V. All rights reserved.
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页码:98 / 104
页数:7
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