2007
DOI: 10.1016/j.tetlet.2007.06.010
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Ratiometric chemosensing of Mg2+ ions by a calix[4]arene diamide derivative

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Cited by 49 publications
(15 citation statements)
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“…5,6 Fluorescent receptors for Mg 2+ , which have diaza-18-crown-6, β-diketone, and calixarene moieties for ion recognition, heve been reported. [7][8][9] However, those receptors could not discriminate Mg 2+ from Ca 2+ due to the similar chemical properties of those two cations. 10 Thus, the development of fluorescent probes with higher specificity and selectivity is being pursued in earnest.…”
Section: Studies Have Indicated That Mgmentioning
confidence: 99%
“…5,6 Fluorescent receptors for Mg 2+ , which have diaza-18-crown-6, β-diketone, and calixarene moieties for ion recognition, heve been reported. [7][8][9] However, those receptors could not discriminate Mg 2+ from Ca 2+ due to the similar chemical properties of those two cations. 10 Thus, the development of fluorescent probes with higher specificity and selectivity is being pursued in earnest.…”
Section: Studies Have Indicated That Mgmentioning
confidence: 99%
“…[3] Recently, various families of Mg 2+ -responsive fluorescent probes have been developed. These probes have receptor groups based upon moieties including a charged b diketone, [4] diaza-18-crown-6, [5] benzo-15-crown-5, [6] calix [4]arene, [7] and imine-linked aromatics.…”
mentioning
confidence: 99%
“…Phenanthroimidazole based systems due to the dramatic supramolecular properties, stability, ease of synthesis, a high extinction coefficient and tuneable photophysical properties have been explored as potential chromophores in a molecular-tweezers system for explosives [45], amine sensors [46,47], fluorophore in a super-radiant laser dye [48], fluorescent tag [49], OLED materials [50][51][52] and chemosensors [53][54][55][56]. The one-step synthesis of phenanthroimidazole derivatives has remarkably increased our own interest to involve a variety of aldehydes that may further extend the way for the introduction of other functionalities and to extend the conjugation for different purposes.…”
Section: Design and Synthesis Of Target Moleculesmentioning
confidence: 99%
“…First, ICT get restricted, due to the formation of a Michael adduct, DCPPI-CNand fluorescence quenching observed at 614 nm. Secondly, the interaction of CNwith second ionophore, the -NH fragment of resultant adduct, DCPPI-CNled to enhance ICT due to an increase in charge density on the phenanthroimidazolyl unit, that finally led to a significant fluorescence enhancement (at 490 nm)[19][20][21][22][23][24][25][26][27][28][29][50][51][52][53][54][55][56][57][58].Moreover, since the changes in optoelectronic behavior of probe in the presence of different anions so rapid it was difficult to obtain a precise kinetic plot. We tried to obtain kinetic plot by the addition of CN -(~20 equiv) to a solution of DCPPI and measured the emission spectra at regular time interval.…”
mentioning
confidence: 99%