<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(6)</volume><submitter>Manoj Kumar S</submitter><pubmed_abstract>A new phenanthridine appended quinoline-based chemoreceptor 5-(5-(quinolin-8-yl)thiophen-2-yl)-tetrahydrodibenzo[a,i]phenanthridine (PHQBA) was successfully synthesized and characterized by &lt;sup>1&lt;/sup>H, &lt;sup>13&lt;/sup>C, and HRMS spectral analyses. The promising chelation-induced process in PHQBA was accelerated by Th&lt;sup>4+&lt;/sup> ions, which impart robust ratiometric green fluorescence at 515 nm. The host-guest complex formed in a 1 : 1 binding stoichiometry between Th&lt;sup>4+&lt;/sup> ions and PHQBA was demonstrated by Jobs plot experiments. The Benesi-Hildebrand (BH) plot was employed to compute the binding constant for the complexation of PHQBA + Th&lt;sup>4+&lt;/sup>, which was determined to be 3.77 × 10&lt;sup>5&lt;/sup> M&lt;sup>-1&lt;/sup>. To comprehend the detection mechanism of PHQBA, DFT, and TDDFT,</pubmed_abstract><journal>RSC advances</journal><pagination>4546-4552</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11808482</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ratiometric discrimination of Th&amp;lt;sup&amp;gt;4+&amp;lt;/sup&amp;gt; ions by a fluorogenic quinoline appended phenanthridine sensor and its applications.</pubmed_title><pmcid>PMC11808482</pmcid><pubmed_authors>Munusamy S</pubmed_authors><pubmed_authors>Manoj Kumar S</pubmed_authors><pubmed_authors>Enbanathan S</pubmed_authors><pubmed_authors>Kulathu Iyer S</pubmed_authors><pubmed_authors>Ranganadin S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ratiometric discrimination of Th&amp;lt;sup&amp;gt;4+&amp;lt;/sup&amp;gt; ions by a fluorogenic quinoline appended phenanthridine sensor and its applications.</name><description>A new phenanthridine appended quinoline-based chemoreceptor 5-(5-(quinolin-8-yl)thiophen-2-yl)-tetrahydrodibenzo[a,i]phenanthridine (PHQBA) was successfully synthesized and characterized by &lt;sup>1&lt;/sup>H, &lt;sup>13&lt;/sup>C, and HRMS spectral analyses. The promising chelation-induced process in PHQBA was accelerated by Th&lt;sup>4+&lt;/sup> ions, which impart robust ratiometric green fluorescence at 515 nm. The host-guest complex formed in a 1 : 1 binding stoichiometry between Th&lt;sup>4+&lt;/sup> ions and PHQBA was demonstrated by Jobs plot experiments. The Benesi-Hildebrand (BH) plot was employed to compute the binding constant for the complexation of PHQBA + Th&lt;sup>4+&lt;/sup>, which was determined to be 3.77 × 10&lt;sup>5&lt;/sup> M&lt;sup>-1&lt;/sup>. To comprehend the detection mechanism of PHQBA, DFT, and TDDFT,</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-26T16:28:41.649Z</modification><creation>2025-04-06T15:14:46.948Z</creation></dates><accession>S-EPMC11808482</accession><cross_references><pubmed>39931419</pubmed><doi>10.1039/d4ra08840a</doi></cross_references></HashMap>