Corentin Rossi, Anne P. Rasmussen, Bérenger Gans, Juraj Jašík, Jan Žabka, Marc Albaret, Hugo Bauduin, Christophe Charrière, Jean-Philippe Dugal, Jérôme Guigand, Catherine Le Bris, Ugo Jacovella
{"title":"iSELECTION: An Instrument to Study the Kinetics of Isomer-Selected Gas-Phase Ion-Molecule Reactions","authors":"Corentin Rossi, Anne P. Rasmussen, Bérenger Gans, Juraj Jašík, Jan Žabka, Marc Albaret, Hugo Bauduin, Christophe Charrière, Jean-Philippe Dugal, Jérôme Guigand, Catherine Le Bris, Ugo Jacovella","doi":"10.1002/cmtd.202500013","DOIUrl":null,"url":null,"abstract":"<p>Distinguishing the chemical reactivity of isomers is a fundamental challenge in chemistry, particularly in cluster chemistry, where the number of possible structures increases dramatically with cluster size. This study presents a novel approach for measuring the kinetics of ion-molecule reactions of laser-ablated species in an isomer-specific fashion. This is achieved by combining drift-tube ion mobility with mass spectrometry, enabling shape selection prior to investigating the chemical reactivity of species of interest. First, the capability of obtaining reaction rate coefficients by studying the nucleophilic addition reactions of small monocyclic carbon rings (<span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>C</mi>\n <mrow>\n <mn>11</mn>\n </mrow>\n <mo>+</mo>\n </msubsup>\n </mrow>\n <annotation>$\\text{C}_{11}^{&#x00026;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;plus;}$</annotation>\n </semantics></math>, <span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>C</mi>\n <mrow>\n <mn>15</mn>\n </mrow>\n <mo>+</mo>\n </msubsup>\n </mrow>\n <annotation>$\\text{C}_{15}^{&#x00026;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;plus;}$</annotation>\n </semantics></math>, and <span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>C</mi>\n <mrow>\n <mn>17</mn>\n </mrow>\n <mo>+</mo>\n </msubsup>\n </mrow>\n <annotation>$\\text{C}_{17}^{&#x00026;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;plus;}$</annotation>\n </semantics></math>) with pyridine, comparing the results with previously reported values is validated. Then the ability to determine isomer-specific reaction rate coefficients using the <span></span><math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>C</mi>\n <mrow>\n <mn>40</mn>\n </mrow>\n <mo>+</mo>\n </msubsup>\n </mrow>\n <annotation>$\\text{C}_{40}^{&#x00026;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;plus;}$</annotation>\n </semantics></math> cluster, where multiple isomers coexist is demonstrated. This highlights the potential of our new instrument for accurately characterizing isomer-specific reactivities in complex chemical systems.</p>","PeriodicalId":72562,"journal":{"name":"Chemistry methods : new approaches to solving problems in chemistry","volume":"5 9","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/cmtd.202500013","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry methods : new approaches to solving problems in chemistry","FirstCategoryId":"1085","ListUrlMain":"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cmtd.202500013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Distinguishing the chemical reactivity of isomers is a fundamental challenge in chemistry, particularly in cluster chemistry, where the number of possible structures increases dramatically with cluster size. This study presents a novel approach for measuring the kinetics of ion-molecule reactions of laser-ablated species in an isomer-specific fashion. This is achieved by combining drift-tube ion mobility with mass spectrometry, enabling shape selection prior to investigating the chemical reactivity of species of interest. First, the capability of obtaining reaction rate coefficients by studying the nucleophilic addition reactions of small monocyclic carbon rings (, , and ) with pyridine, comparing the results with previously reported values is validated. Then the ability to determine isomer-specific reaction rate coefficients using the cluster, where multiple isomers coexist is demonstrated. This highlights the potential of our new instrument for accurately characterizing isomer-specific reactivities in complex chemical systems.