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    <name>Article</name>
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          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>A Selective Excited-State Intramolecular-Proton-Transfer (ESIPT) Sensor for Copper(II) Based on Chelation-Enhanced Quenching and Off-On Detection of Amino Acids</text>
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              <text>amino acids; chelation; ESIPT; fluorescence; ratiometry</text>
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          <description>An account of the resource</description>
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              <text>We report the synthesis of 2-(4,5-diphenyl-1H-imidazole-2-yl)phenol (TPI-9) as an interesting fluorescent molecule displaying Excited-State Intramolecular-Proton-Transfer (ESIPT) with stokes shift of 120 nm. Phenolic compounds with the ability to form intramolecular hydrogen bonds and subsequent proton transfer are known as ESIPT fluorophores. Proton accepting ability can increase significantly by tailoring electron-donating groups. With the assistance of an environment-friendly organocatalyst, 10-camphor sulfonic acid (10-CSA), TPI-9 was synthesized to introduce substituents with electron-donating abilities to develop an efficient ESIPT mechanism. Factors influencing the emission, such as solvent, pH, and metal ions, are investigated. Quenching of fluorescence by Cu2+ through chelation enhancement quenching effect with a high selectivity allowed the establishment of a Cu2+ sensor with an LoD of 0.57 ppm and a ratiometric estimation with an LoD of 0.73 ppm. Metal binding (2 : 1) stoichiometry and quenching constant (0.0072 mol?1s?1) are calculated from Job's and Stern-Volmer plots. Density functional theory (DFT) calculations are in accordance with the experimental results. Competitive replacement of TPI-9 by amino acids restores ESIPT, consequently, the fluorescence. Thus, an off-on fluorescence sensor for amino acid estimation is developed under 1 minute incubation. A linear relationship between amino acid concentration and fluorescence intensity is in 0-20 ?g/mL range, and the LoD is less than 2.2 ?g/mL.  2023 Wiley-VCH GmbH.</text>
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          <name>Creator</name>
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              <text>Devasia J.; Joy F.; Nizam A.</text>
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              <text>Chemistry - A European Journal, Vol-29, No. 25</text>
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              <text>John Wiley and Sons Inc</text>
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          <name>Date</name>
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              <text>2023-01-01</text>
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              <text>&lt;a href="https://doi.org/10.1002/chem.202203652" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1002/chem.202203652&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85150635996&amp;amp;doi=10.1002%2Fchem.202203652&amp;amp;partnerID=40&amp;amp;md5=91ca8a52442f09e3d2b8039c2a01004a" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85150635996&amp;amp;doi=10.1002%2fchem.202203652&amp;amp;partnerID=40&amp;amp;md5=91ca8a52442f09e3d2b8039c2a01004a&lt;/a&gt;</text>
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              <text>ISSN: 9476539; PubMed ID: 36750756; CODEN: CEUJE</text>
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              <text>Online</text>
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              <text>English</text>
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              <text>Devasia J., Department of Chemistry, CHRIST (Deemed to be University) Hosur road, DRC post, Bangalore, 560029, India; Joy F., Department of Chemistry, CHRIST (Deemed to be University) Hosur road, DRC post, Bangalore, 560029, India; Nizam A., Department of Chemistry, CHRIST (Deemed to be University) Hosur road, DRC post, Bangalore, 560029, India</text>
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