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Formation of the C4Hn+ (n=2-5) ions upon ionization of acetylene clusters in helium droplets

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dc.contributor.authorMoon, Cheol Joo-
dc.contributor.authorErukala, Swetha-
dc.contributor.authorFeinberg, Alexandra J.-
dc.contributor.authorSingh, Amandeep-
dc.contributor.authorChoi, Myong Yong-
dc.contributor.authorVilesov, Andrey F.-
dc.date.accessioned2023-08-07T01:41:17Z-
dc.date.available2023-08-07T01:41:17Z-
dc.date.issued2023-06-
dc.identifier.issn0021-9606-
dc.identifier.issn1089-7690-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/67423-
dc.description.abstractInfrared (IR) spectroscopy using ultracold helium nanodroplet matrices has proven to be a powerful method to interrogate encapsulated ions, molecules, and clusters. Due to the helium droplets' high ionization potential, optical transparency, and ability to pick up dopant molecules, the droplets offer a unique modality to probe transient chemical species produced via photo- or electron impact ionization. In this work, helium droplets were doped with acetylene molecules and ionized via electron impact. Ion-molecule reactions within the droplet volume yield larger carbo-cations that were studied via IR laser spectroscopy. This work is focused on cations containing four carbon atoms. The spectra of C4H2+, C4H3+, and C4H5+ are dominated by diacetylene, vinylacetylene, and methylcyclopropene cations, respectively, which are the lowest energy isomers. On the other hand, the spectrum of C4H4+ ions hints at the presence of several co-existing isomers, the identity of which remains to be elucidated.-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Institute of Physics-
dc.titleFormation of the C4Hn+ (n=2-5) ions upon ionization of acetylene clusters in helium droplets-
dc.title.alternativeFormation of the C4Hn +(n = 2-5) ions upon ionization of acetylene clusters in helium droplets-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1063/5.0150700-
dc.identifier.scopusid2-s2.0-85163002825-
dc.identifier.wosid001027658300006-
dc.identifier.bibliographicCitationThe Journal of Chemical Physics, v.158, no.22-
dc.citation.titleThe Journal of Chemical Physics-
dc.citation.volume158-
dc.citation.number22-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryPhysics, Atomic, Molecular & Chemical-
dc.subject.keywordPlusINFRARED PHOTODISSOCIATION SPECTROSCOPY-
dc.subject.keywordPlusUNIMOLECULAR DECOMPOSITION-
dc.subject.keywordPlusIR SPECTROSCOPY-
dc.subject.keywordPlusRADICAL-CATION-
dc.subject.keywordPlusMOLECULAR-IONS-
dc.subject.keywordPlusRATE CONSTANTS-
dc.subject.keywordPlusDYNAMICS-
dc.subject.keywordPlusPHOTOIONIZATION-
dc.subject.keywordPlusETHYLENE-
dc.subject.keywordPlusDIMERS-
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