<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>130(6)</volume><submitter>Rohdenburg M</submitter><pubmed_abstract>Electrophilic dodecaborate fragment ions [B&lt;sub>12&lt;/sub>X&lt;sub>11&lt;/sub>]&lt;sup>-&lt;/sup> are among the most reactive anions known and are capable of converting inert reagents to charged compounds through covalent bonding. In this study, we investigate the reactivity of [B&lt;sub>12&lt;/sub>X&lt;sub>11&lt;/sub>]&lt;sup>-&lt;/sup> (X = Br, I) with a series of hydrocarbons in two environments: (1) in the gas phase, using ion-molecule reactions and collision-induced dissociation (CID), and (2) at vacuum/solid interfaces, via fragment ion deposition onto surface layers of reagents. In the gas phase, &lt;i>n-&lt;/i>alkyl groups of hydrocarbons are bound to [B&lt;sub>12&lt;/sub>X&lt;sub>11&lt;/sub>]&lt;sup>-&lt;/sup> via the substitution of a proton by the electrophilic vacant boron atom. However, hydrocarbons with double and triple bonds are</pubmed_abstract><journal>The journal of physical chemistry. A</journal><pagination>1364-1374</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12908116</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Functionalization of Saturated and Unsaturated Hydrocarbons with Electrophilic Anions [B&amp;lt;sub&amp;gt;12&amp;lt;/sub&amp;gt;X&amp;lt;sub&amp;gt;11&amp;lt;/sub&amp;gt;]&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; (X = Br, I) in the Gas Phase and at Interfaces.</pubmed_title><pmcid>PMC12908116</pmcid><pubmed_authors>Rohdenburg M</pubmed_authors><pubmed_authors>Monakhov K</pubmed_authors><pubmed_authors>Warneke J</pubmed_authors><pubmed_authors>Kaur J</pubmed_authors><pubmed_authors>Benny AP</pubmed_authors><pubmed_authors>Petrovskii S</pubmed_authors><pubmed_authors>Ma X</pubmed_authors><pubmed_authors>Behrend KA</pubmed_authors><pubmed_authors>Galligan AJ</pubmed_authors><pubmed_authors>Kenttamaa HI</pubmed_authors></additional><is_claimable>false</is_claimable><name>Functionalization of Saturated and Unsaturated Hydrocarbons with Electrophilic Anions [B&amp;lt;sub&amp;gt;12&amp;lt;/sub&amp;gt;X&amp;lt;sub&amp;gt;11&amp;lt;/sub&amp;gt;]&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; (X = Br, I) in the Gas Phase and at Interfaces.</name><description>Electrophilic dodecaborate fragment ions [B&lt;sub>12&lt;/sub>X&lt;sub>11&lt;/sub>]&lt;sup>-&lt;/sup> are among the most reactive anions known and are capable of converting inert reagents to charged compounds through covalent bonding. In this study, we investigate the reactivity of [B&lt;sub>12&lt;/sub>X&lt;sub>11&lt;/sub>]&lt;sup>-&lt;/sup> (X = Br, I) with a series of hydrocarbons in two environments: (1) in the gas phase, using ion-molecule reactions and collision-induced dissociation (CID), and (2) at vacuum/solid interfaces, via fragment ion deposition onto surface layers of reagents. In the gas phase, &lt;i>n-&lt;/i>alkyl groups of hydrocarbons are bound to [B&lt;sub>12&lt;/sub>X&lt;sub>11&lt;/sub>]&lt;sup>-&lt;/sup> via the substitution of a proton by the electrophilic vacant boron atom. However, hydrocarbons with double and triple bonds are</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-15T21:28:01.735Z</modification><creation>2026-07-09T10:14:27.437Z</creation></dates><accession>S-EPMC12908116</accession><cross_references><pubmed>41612766</pubmed><doi>10.1021/acs.jpca.5c08384</doi></cross_references></HashMap>