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              <text>Colorimetric and theoretical investigation of coumarin based chemosensor for selective detection of fluoride</text>
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              <text>Chemosensor; Colorimetric; Coumarin; Density functional theory; Hydrogen bonding; Selective detection</text>
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              <text>Coumarin based Sensor 1 has been designed and synthesized to recognize fluoride ion visually with high selectivity and sensitivity over other anionic analytes through color change from very faint yellow to pink in acetonitrile. The probable binding phenomenon in solution phase has been explained by 1H NMR study of sensor 1 with different concentration of fluoride ions. The binding constant of the sensor 1 with fluoride has been determined as 3.9 104 M?1 and the lower detection limit 6.5 M of the sensor 1 towards fluoride, which has made the sensor 1 as a promising backbone for selective detection of fluoride. For the practical application, test strips based on sensor 1 were fabricated, which could act as a convenient and efficient naked eye F?test kits. The experimentally observed absorption maxima along with its binding nature with fluoride ions also have been supported through theoretical calculations using density functional theory (DFT) calculations.  2022</text>
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          <name>Creator</name>
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              <text>Maity S.; Maity A.C.; kumar Das A.; Roymahapatra G.; Goswami S.; Mandal T.K.</text>
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              <text>Journal of Molecular Structure, Vol-1264</text>
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              <text>Elsevier B.V.</text>
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              <text>2022-01-01</text>
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              <text>&lt;a href="https://doi.org/10.1016/j.molstruc.2022.133228" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1016/j.molstruc.2022.133228&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85130392315&amp;amp;doi=10.1016%2Fj.molstruc.2022.133228&amp;amp;partnerID=40&amp;amp;md5=c850a9e7a11d997650ace6b91ceac4e7" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85130392315&amp;amp;doi=10.1016%2fj.molstruc.2022.133228&amp;amp;partnerID=40&amp;amp;md5=c850a9e7a11d997650ace6b91ceac4e7&lt;/a&gt;</text>
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              <text>ISSN: 222860; CODEN: JMOSB</text>
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              <text>Online</text>
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              <text>English</text>
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              <text>Maity S., Department of Applied Sciences, Haldia Institute of Technology, Hatiberia, West Bengal, Haldia, 721657, India; Maity A.C., Department of Chemistry, Indian Institute of Engineering Science and Technology, Shibpur, West Bengal, Howrah, 711103, India; kumar Das A., Department of Chemistry, CHRIST (Deemed to be University), Hosur Road, Karnataka, Bengaluru, 560029, India; Roymahapatra G., Department of Applied Sciences, Haldia Institute of Technology, Hatiberia, West Bengal, Haldia, 721657, India; Goswami S., Department of Chemistry, Indian Institute of Engineering Science and Technology, Shibpur, West Bengal, Howrah, 711103, India; Mandal T.K., Vidyasagar University, Rangamati, West Bengal, Midnapore, 721102, India</text>
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