2013
DOI: 10.1016/j.saa.2013.07.069
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Glutamine-containing “turn-on” fluorescence sensor for the highly sensitive and selective detection of chromium (III) ion in water

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Cited by 28 publications
(8 citation statements)
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“…However, the lack of Cr(III) may cause dysglycemia and coronary arteriosclerosis, which increase the risk of diabetes and cardiovascular diseases. [41][42][43] In addition, Cr(III) and Cr(VI) can transform into each other under certain conditions, and Cr(VI) and its compounds are toxic. Therefore, it is of great signi¯cance to detect Cr(III) for human safety, environmental monitoring and life science research.…”
Section: Introductionmentioning
confidence: 99%
“…However, the lack of Cr(III) may cause dysglycemia and coronary arteriosclerosis, which increase the risk of diabetes and cardiovascular diseases. [41][42][43] In addition, Cr(III) and Cr(VI) can transform into each other under certain conditions, and Cr(VI) and its compounds are toxic. Therefore, it is of great signi¯cance to detect Cr(III) for human safety, environmental monitoring and life science research.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4] In recent decades, novel uorescence chemosensors for metal ions, such as chromium, zinc, aluminum and copper, have gained importance due to their operational simplicity, high selectivity, sensitivity and rapidity. [5][6][7][8] Although the uorescence intensity of chemosensors quenched in the presence of Cr(III) has been reported, few papers are available on the uorescence enhancement of chemosensors with Cr(III) ions. [9][10][11][12][13][14] Among uorescent chemosensors, Bodipy sensors have been extensively studied for numerous applications (optic, sensor and dye) to a number of functional materials owing to their unique photophysical properties, such as sharp absorption prole, high uorescence quantum yields, good photo-stability and large extinction coefficients.…”
Section: Introductionmentioning
confidence: 99%
“…[13][14][15] Great efforts have also been made on designing turn-on sensors because turn-off sensors tend to produce a low signal output upon binding and are therefore prone to interfere with the temporal separation of similar complexes with timeresolved uorometry. [16][17][18][19] Unfortunately, most turn-on chemosensors for detection of Cr 3+ have focused on rhodamine derivatives, which can probe Cr 3+ by conversion of the non-uorescent rhodamine spirolactam to the highly uorescent ring-open amide form upon binding. [20][21][22][23][24][25] Furthermore, the long equilibrium time and high limits of detection of rhodamine derivatives do not satisfy the requirement of fast-response and high sensitivity under pharmacological conditions.…”
Section: Introductionmentioning
confidence: 99%