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Resonance enhanced multiphoton ionization of nucleosides by using pulsed-laser desorption in supersonic beam mass spectrometry

dc.contributor.authorLi, Liangen_US
dc.contributor.authorLubman, David M.en_US
dc.date.accessioned2006-04-07T20:51:04Z
dc.date.available2006-04-07T20:51:04Z
dc.date.issued1989-04-01en_US
dc.identifier.citationLi, Liang, Lubman, David M. (1989/04/01)."Resonance enhanced multiphoton ionization of nucleosides by using pulsed-laser desorption in supersonic beam mass spectrometry." International Journal of Mass Spectrometry and Ion Processes 88(2-3): 197-210. <http://hdl.handle.net/2027.42/27986>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TG6-44FMW08-N6/2/73c45aee1d561dd77836dfa84bf61a85en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27986
dc.description.abstractPulsed-laser desorption is used as a means of volatilizing nucleosides into the gas phase for entrainment into a supersonic jet expansion. These species are then studied in a time-of-flight mass spectrometer by resonance enhanced multiphoton ionization. Using this combination of techniques either relatively soft ionization or controlled fragmentation can be produced. The degree of molecule ion formation is shown to be relatively strong compared to other soft ionization methods such as FAB/MS, SIMS, FD or FI. In addition, the resulting fragmentation produces ions that are characteristic of the structure of the nucleoside. It is further demonstrated that such fragmentation can be used to discrimination between isomeric nucleosides and also between ribose and deoxyribose sugar groups.en_US
dc.format.extent920815 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleResonance enhanced multiphoton ionization of nucleosides by using pulsed-laser desorption in supersonic beam mass spectrometryen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055 U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055 U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27986/1/0000419.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0168-1176(89)85016-5en_US
dc.identifier.sourceInternational Journal of Mass Spectrometry and Ion Processesen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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