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A dual-responsive fluorescent probe for detection of H2S and Cu2+ based on rhodamine-naphthalimide and cell imaging
被引:27
|作者:
Ai, Yin
[1
]
Zhu, Zifan
[1
]
Ding, Haichang
[1
]
Fan, Congbin
[1
]
Liu, Gang
[1
]
Pu, Shouzhi
[1
,2
]
机构:
[1] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
[2] Yuzhang Normal Univ, Dept Ecol & Environm, Nanchang 330103, Jiangxi, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Dual-responsive;
Fluorescent probe;
Rhodamine;
Naphthalimide;
H2S;
Cu2+;
HYDROGEN-SULFIDE;
TURN-ON;
RATIOMETRIC DETECTION;
SENSITIVE DETECTION;
LIVING CELLS;
C-C;
CHEMOSENSOR;
EMISSION;
FORMALDEHYDE;
IONS;
D O I:
10.1016/j.jphotochem.2022.113801
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A highly selective and sensitive fluorescence probe (DTR-1) for simultaneously detecting H2S and Cu2+ with different fluorescence signals was synthesized. DTR-1 displayed remarkable fluorescence enhancement (560 nm, 34-fold) when H2S was added under excitation of 410 nm with the solution's color change from dark to green. The limit of detection (LOD) for H2S was calculated to be 0.035 mu M. By contrast, the addition of Cu2+ enhanced obviously the emission intensity of DTR-1 with the maximal peak at 630 nm and color change from colorless to orange. LOD for Cu2+ was determined to be 0.16 mu M. The sensing mechanism for H2S and Cu2+ in DMF/PBS (9/ 1, v/v, pH = 7.4) was studied by H-1 NMR and ESI-MS. Furthermore, the potential application of DTR-1 in biological systems had been demonstrated through imaging of living cells.
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