2014
DOI: 10.1016/j.jlumin.2014.06.023
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A chromone Schiff-base as Al(III) selective fluorescent and colorimetric chemosensor

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Cited by 38 publications
(3 citation statements)
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“…The wide range of chemical reactivity of hydrazones allows their application in the detection of anions, cations, and other species [10]. Some hydrazone-based chemosensors have weak fluorescence because of quenching effects such as E/Z double bond isomerization in the excited state; photoinduced electron transfer (PET) process (excited electron is transferred from donor to acceptor; generating a charge separation, i.e., redox reaction takes place in excited state); [11] excited state intramolecular proton transfer (ESIPT) process (photoexcited molecule relax their energy through tautomerization by transfer a proton); and others [12,13]. The main objective for this class of chemosensors is inhibiting the quenching effects after interaction with some analytes promoting a fluorescence state.…”
Section: Hydrazone-based Compounds As Fluorescent Chemosensorsmentioning
confidence: 99%
“…The wide range of chemical reactivity of hydrazones allows their application in the detection of anions, cations, and other species [10]. Some hydrazone-based chemosensors have weak fluorescence because of quenching effects such as E/Z double bond isomerization in the excited state; photoinduced electron transfer (PET) process (excited electron is transferred from donor to acceptor; generating a charge separation, i.e., redox reaction takes place in excited state); [11] excited state intramolecular proton transfer (ESIPT) process (photoexcited molecule relax their energy through tautomerization by transfer a proton); and others [12,13]. The main objective for this class of chemosensors is inhibiting the quenching effects after interaction with some analytes promoting a fluorescence state.…”
Section: Hydrazone-based Compounds As Fluorescent Chemosensorsmentioning
confidence: 99%
“…The hydrazone backbone includes an imine carbon with an electrophile character, two nucleophilic nitrogen in both amine and imine groups, and the possible isomerization of the C=N double bond from the conjugation of imine and acid N-H. In certain cases, the long response time or low sensitivity in the presence of analytes is responsible for the weak fluorescence because of quenching effects, such as double-bond isomerization in the excited state, the photoinduced electron transfer (PET) process or the excited-state intramolecular proton-transfer (ESIPT) process [12,13]. Usually, hydrazones are anchored to other fluorophores or aromatic structures such as naphthalimides or coumarins [14][15][16][17][18].…”
Section: Introductionmentioning
confidence: 99%
“…1 The normal concentration range for aluminum ions in biological systems is narrow, with both deciency and excess causing many pathological states, such as Alzheimer's disease, Parkinson's disease, chronic renal failure, bone soening and smoking related diseases. [2][3][4][5][6] Since there is a close association between Al 3+ and human health, developing uorescent chemosensors with high selectivity and sensitivity for detecting trace amounts of Al 3+ has attracted increasing attention.…”
Section: Introductionmentioning
confidence: 99%