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dc.contributor.authorBayindir, S. and Saracoglu, N.
dc.date.accessioned2021-04-08T12:08:49Z
dc.date.available2021-04-08T12:08:49Z
dc.date.issued2016
dc.identifier10.1039/c6ra16192h
dc.identifier.issn20462069
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84981323604&doi=10.1039%2fc6ra16192h&partnerID=40&md5=270e684932b8f796e8c252038f8d2cfb
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4688
dc.description.abstractIndole derivatives are of great importance because of their biological activity and application in technology. This study explores the synthesis of 2-alkylated indoles derivatives and 2,2′-bis(indolyl)methanes, and their application in anion sensing. The synthesis of a wide range of 2-alkylated indoles and some 2,2′-bis(indolyl)methanes, which cannot be synthesized by previously reported methods, was for the first time accomplished employing dipole exchange of the indole ring towards electrophilic substitution. Some of the indole derivatives exhibited selective recognition and sensing ability towards F- and HSO4- anions through naked-eye detectable color changes. The sensing details of the indole derivatives were also evaluated using UV-Vis spectroscopy and 1H NMR titration techniques. © 2016 The Royal Society of Chemistry.
dc.language.isoEnglish
dc.sourceRSC Advances
dc.titleA facile one-pot method to synthesise 2-alkylated indole and 2,2′-bis(indolyl)methane derivatives using ketones as electrophiles and their anion sensing ability


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