<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>63(52)</volume><submitter>Caporaletti F</submitter><funding>Fonds De La Recherche Scientifique - FNRS</funding><pubmed_abstract>Using fluorinated mono-alcohols, in particular hexafluoro-isopropanol (HFIP), as a solvent can enhance chemical reaction rates in a spectacular manner. Previous work has shown evidence that this enhancement is related to the hydrogen-bond structure of these liquids. Here, we investigate the hydrogen-bond dynamics of HFIP and compare it to that of its non-fluorinated analog, isopropanol. Ultrafast infrared spectroscopy experiments show that the dynamics of individual hydrogen-bonds is about twice as slow in HFIP as in isopropanol. Surprisingly, from dielectric spectroscopy we find the opposite behavior for the dynamics of hydrogen-bonded clusters: collective rearrangements are 3 times faster in HFIP than in isopropanol. This difference indicates that the hydrogen-bonded clusters in HFIP are</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pagination>e202416091</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11656151</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Fast Collective Hydrogen-Bond Dynamics in Hexafluoroisopropanol Related to its Chemical Activity.</pubmed_title><pmcid>PMC11656151</pmcid><pubmed_authors>Hunger J</pubmed_authors><pubmed_authors>Caporaletti F</pubmed_authors><pubmed_authors>Gunkel L</pubmed_authors><pubmed_authors>Woutersen S</pubmed_authors><pubmed_authors>Fernandez-Ibanez MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fast Collective Hydrogen-Bond Dynamics in Hexafluoroisopropanol Related to its Chemical Activity.</name><description>Using fluorinated mono-alcohols, in particular hexafluoro-isopropanol (HFIP), as a solvent can enhance chemical reaction rates in a spectacular manner. Previous work has shown evidence that this enhancement is related to the hydrogen-bond structure of these liquids. Here, we investigate the hydrogen-bond dynamics of HFIP and compare it to that of its non-fluorinated analog, isopropanol. Ultrafast infrared spectroscopy experiments show that the dynamics of individual hydrogen-bonds is about twice as slow in HFIP as in isopropanol. Surprisingly, from dielectric spectroscopy we find the opposite behavior for the dynamics of hydrogen-bonded clusters: collective rearrangements are 3 times faster in HFIP than in isopropanol. This difference indicates that the hydrogen-bonded clusters in HFIP are</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-04T01:52:01.554Z</modification><creation>2025-04-04T01:52:01.554Z</creation></dates><accession>S-EPMC11656151</accession><cross_references><pubmed>39388385</pubmed><doi>10.1002/anie.202416091</doi></cross_references></HashMap>