<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Ellin NR</submitter><funding>National Institute of General Medical Sciences</funding><pubmed_abstract>This work summarizes the criteria for a useful reagent for ion/ion proton transfer in an electrodynamic ion trap with specific emphasis on proton transfer to high mass multiply-charged analyte ions. A readily available and ionizable weak base of relatively high mass meets the criteria. The protonated form of an extensively fluorinated 10-carbon primary amine (1&lt;i>H&lt;/i>,1&lt;i>H&lt;/i>,2&lt;i>H&lt;/i>,2&lt;i>H&lt;/i>-perfluorodecylamine, PFDA) is demonstrated to serve as a useful reagent for proton transfer to negatively-charged proteins and oligonucleotides. The behavior of protonated PFDA is compared with that of protonated 1,8-bis(dimethylamino)naphthalene (proton sponge) with respect to the tendency for proton transfer &lt;i>versus&lt;/i> attachment in ion/ion reactions with a common multiply-deprotonated prot</pubmed_abstract><journal>The Analyst</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12935111</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Proton transfer reagent cations for ion-ion charge state manipulation of high mass negatively-charged analytes in an electrodynamic ion trap.</pubmed_title><pmcid>PMC12935111</pmcid><funding_grant_id>R35-153191</funding_grant_id><pubmed_authors>McLuckey SA</pubmed_authors><pubmed_authors>Faye BKS</pubmed_authors><pubmed_authors>Horn SA</pubmed_authors><pubmed_authors>Koers AM</pubmed_authors><pubmed_authors>Ellin NR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proton transfer reagent cations for ion-ion charge state manipulation of high mass negatively-charged analytes in an electrodynamic ion trap.</name><description>This work summarizes the criteria for a useful reagent for ion/ion proton transfer in an electrodynamic ion trap with specific emphasis on proton transfer to high mass multiply-charged analyte ions. A readily available and ionizable weak base of relatively high mass meets the criteria. The protonated form of an extensively fluorinated 10-carbon primary amine (1&lt;i>H&lt;/i>,1&lt;i>H&lt;/i>,2&lt;i>H&lt;/i>,2&lt;i>H&lt;/i>-perfluorodecylamine, PFDA) is demonstrated to serve as a useful reagent for proton transfer to negatively-charged proteins and oligonucleotides. The behavior of protonated PFDA is compared with that of protonated 1,8-bis(dimethylamino)naphthalene (proton sponge) with respect to the tendency for proton transfer &lt;i>versus&lt;/i> attachment in ion/ion reactions with a common multiply-deprotonated prot</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-16T20:47:54.576Z</modification><creation>2026-07-10T03:13:06.457Z</creation></dates><accession>S-EPMC12935111</accession><cross_references><pubmed>41739648</pubmed><doi>10.1039/d5an01354b</doi></cross_references></HashMap>