<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xiang H</submitter><funding>Jiaxing Public Welfare Research Project</funding><funding>National Natural Science Foundation of China</funding><funding>Zhejiang Provincial Natural Science Foundation</funding><pagination>7499</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9653583</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(21)</volume><pubmed_abstract>Hydrogen sulfide (H&lt;sub>2&lt;/sub>S) as small molecular signal messenger plays key functions in numerous biological processes. The imaging detection of intracellular hydrogen sulfide is of great significance. In this work, a ratiometric fluorescent probe &lt;b>BH&lt;/b> based on an asymmetric BODIPY dye for detection of H&lt;sub>2&lt;/sub>S was designed and synthesized. After the interaction with hydrogen sulfide, probe display colorimetric and ratiometric fluorescence response, with its maximum emission fluorescence wavelength red-shifted from 542 nm to 594 nm, which is attributed to the sequential nucleophilic reaction of H&lt;sub>2&lt;/sub>S leading to enhanced molecular conjugation after ring formation of the BODIPY skeleton. A special response mechanism has been fully investigated by NMR titration and MS,</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>A New Ratiometric Fluorescent Probe Based on BODIPY for Highly Selective Detection of Hydrogen Sulfide.</pubmed_title><pmcid>PMC9653583</pmcid><funding_grant_id>LY20B060009</funding_grant_id><funding_grant_id>2021AY10070</funding_grant_id><funding_grant_id>22071082</funding_grant_id><funding_grant_id>21606102</funding_grant_id><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Ye T</pubmed_authors><pubmed_authors>Xiang H</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Liu D</pubmed_authors><pubmed_authors>Zhou H</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Li L</pubmed_authors></additional><is_claimable>false</is_claimable><name>A New Ratiometric Fluorescent Probe Based on BODIPY for Highly Selective Detection of Hydrogen Sulfide.</name><description>Hydrogen sulfide (H&lt;sub>2&lt;/sub>S) as small molecular signal messenger plays key functions in numerous biological processes. The imaging detection of intracellular hydrogen sulfide is of great significance. In this work, a ratiometric fluorescent probe &lt;b>BH&lt;/b> based on an asymmetric BODIPY dye for detection of H&lt;sub>2&lt;/sub>S was designed and synthesized. After the interaction with hydrogen sulfide, probe display colorimetric and ratiometric fluorescence response, with its maximum emission fluorescence wavelength red-shifted from 542 nm to 594 nm, which is attributed to the sequential nucleophilic reaction of H&lt;sub>2&lt;/sub>S leading to enhanced molecular conjugation after ring formation of the BODIPY skeleton. A special response mechanism has been fully investigated by NMR titration and MS,</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-25T23:23:23.731Z</modification><creation>2025-04-06T09:22:32.159Z</creation></dates><accession>S-EPMC9653583</accession><cross_references><pubmed>36364325</pubmed><doi>10.3390/molecules27217499</doi></cross_references></HashMap>