<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>45</viewCount><searchCount>0</searchCount></scores><additional><submitter>Biswas PK</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>DFG</funding><pagination>14095-14099</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7702118</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(62)</volume><pubmed_abstract>The dynamics of hydrogen bonding do not only play an important role in many biochemical processes but also in Nature's multicomponent machines. Here, a three-component nanorotor is presented where both the self-assembly and rotational dynamics are guided by hydrogen bonding. In the rate-limiting step of the rotational exchange, two phenolic O-H-N,N&lt;sub>(phenanthroline)&lt;/sub> hydrogen bonds are cleaved, a process that was followed by variable-temperature &lt;sup>1&lt;/sup> H NMR spectroscopy. Activation data (ΔG&lt;sup>≠&lt;/sup> &lt;sub>298&lt;/sub> =46.7 kJ mol&lt;sup>-1&lt;/sup> at 298 K, ΔH&lt;sup>≠&lt;/sup> =55.3 kJ mol&lt;sup>-1&lt;/sup> , and ΔS&lt;sup>≠&lt;/sup> =28.8 J mol&lt;sup>-1&lt;/sup>  K&lt;sup>-1&lt;/sup> ) were determined, furnishing a rotational exchange frequency of k&lt;sub>298&lt;/sub> =40.0 kHz. Fully reversible disassembly/assembly of the nanorotor was achieved by addition of 5.0 equivalents of trifluoroacetic acid (TFA)/1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) over three cycles.</pubmed_abstract><journal>Chemistry (Weinheim an der Bergstrasse, Germany)</journal><pubmed_title>Dynamics of Hydrogen Bonding in Three-Component Nanorotors.</pubmed_title><pmcid>PMC7702118</pmcid><funding_grant_id>Schm 647/20-2</funding_grant_id><pubmed_authors>Saha S</pubmed_authors><pubmed_authors>Schmittel M</pubmed_authors><pubmed_authors>Goswami A</pubmed_authors><pubmed_authors>Biswas PK</pubmed_authors><view_count>45</view_count></additional><is_claimable>false</is_claimable><name>Dynamics of Hydrogen Bonding in Three-Component Nanorotors.</name><description>The dynamics of hydrogen bonding do not only play an important role in many biochemical processes but also in Nature's multicomponent machines. Here, a three-component nanorotor is presented where both the self-assembly and rotational dynamics are guided by hydrogen bonding. In the rate-limiting step of the rotational exchange, two phenolic O-H-N,N&lt;sub>(phenanthroline)&lt;/sub> hydrogen bonds are cleaved, a process that was followed by variable-temperature &lt;sup>1&lt;/sup> H NMR spectroscopy. Activation data (ΔG&lt;sup>≠&lt;/sup> &lt;sub>298&lt;/sub> =46.7 kJ mol&lt;sup>-1&lt;/sup> at 298 K, ΔH&lt;sup>≠&lt;/sup> =55.3 kJ mol&lt;sup>-1&lt;/sup> , and ΔS&lt;sup>≠&lt;/sup> =28.8 J mol&lt;sup>-1&lt;/sup>  K&lt;sup>-1&lt;/sup> ) were determined, furnishing a rotational exchange frequency of k&lt;sub>298&lt;/sub> =40.0 kHz. Fully reversible disassembly/assembly of the nanorotor was achieved by addition of 5.0 equivalents of trifluoroacetic acid (TFA)/1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) over three cycles.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2024-02-15T13:36:04.469Z</modification><creation>2021-02-20T10:32:07Z</creation></dates><accession>S-EPMC7702118</accession><cross_references><pubmed>32744381</pubmed><doi>10.1002/chem.202002877</doi></cross_references></HashMap>