2014
DOI: 10.1039/c4nj00412d
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Optical chemosensors for Hg2+from terthiophene appended rhodamine derivatives: FRET based molecular and in situ hybrid gold nanoparticle sensors

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Cited by 27 publications
(11 citation statements)
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“…However, these chemosensors cannot differentiate the fluorescent signal from Ca 2+ and Mg 2+ due to similar binding events of crown ethers with these two metal ions. Taking advantage of a similar principle, rhodamine-functionalized AuNPs were also employed to develop “turn-on” fluorescent sensors for sensitive detection of Hg 2+ [80] and Zn 2+ [81], with a LOD of 0.32 μM and 0.05 mg/L, respectively. A fluorescence resonance energy transfer (FRET) -based “turn-off” sensor for Cu 2+ has been recently developed using FITC modified AuNPs by Hormozi-Nezhad et al [82].…”
Section: Noble Metal Nanomaterials-based Fluorescent Nanoprobes Fomentioning
confidence: 99%
“…However, these chemosensors cannot differentiate the fluorescent signal from Ca 2+ and Mg 2+ due to similar binding events of crown ethers with these two metal ions. Taking advantage of a similar principle, rhodamine-functionalized AuNPs were also employed to develop “turn-on” fluorescent sensors for sensitive detection of Hg 2+ [80] and Zn 2+ [81], with a LOD of 0.32 μM and 0.05 mg/L, respectively. A fluorescence resonance energy transfer (FRET) -based “turn-off” sensor for Cu 2+ has been recently developed using FITC modified AuNPs by Hormozi-Nezhad et al [82].…”
Section: Noble Metal Nanomaterials-based Fluorescent Nanoprobes Fomentioning
confidence: 99%
“…Rhen was synthesized according to a procedure in the literature with slight modification . Rhodamine B (0.40 g, 0.84 mmol) was dissolved in 10 mL of MeOH, and ethylenediamine (0.44 mL, excess) was added dropwise to the solution and refluxed until the solution lost its red color.…”
Section: Methodsmentioning
confidence: 99%
“…Functional pendant groups carrying an amine or a carboxylic acid were attached respectively to trimer carboxylic acid [ 303 , 304 , 377 , 378 , 379 , 380 , 381 ] or amine ( Scheme 20 , I and II) [ 207 , 208 , 209 , 382 ]. The amide formation occurs on the side group of the central thiophene either before [ 377 , 378 , 379 , 380 ] or after [ 207 , 381 , 382 ] the formation of the trimer and it is typically achieved by carboxylic acid activation by acyl chloride [ 207 , 208 , 209 , 378 ] or a carbodiimide coupling agent [ 377 , 379 , 380 , 381 ], followed by amine nucleophilic substitution. Instead, the reaction between a trimer diester and hydrazine leads to the formation of a pyridazinedione pendant group on the central unit ( Scheme 20 , III) [ 366 , 367 ].…”
Section: Trimer Structuresmentioning
confidence: 99%