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Raman longitudinal acoustic mode (LAM) studies of folded-chain morphology in poly(ethylene oxide) (PEO). I. Normal mode analysis of LAM of a helical-chain oligomer of PEO

dc.contributor.authorSong, Kigooken_US
dc.contributor.authorKrimm, Samuelen_US
dc.date.accessioned2006-04-28T18:20:08Z
dc.date.available2006-04-28T18:20:08Z
dc.date.issued1990-01-15en_US
dc.identifier.citationSong, Kigook; Krimm, Samuel (1990)."Raman longitudinal acoustic mode (LAM) studies of folded-chain morphology in poly(ethylene oxide) (PEO). I. Normal mode analysis of LAM of a helical-chain oligomer of PEO." Journal of Polymer Science Part B: Polymer Physics 28(1): 35-50. <http://hdl.handle.net/2027.42/38859>en_US
dc.identifier.issn0887-6266en_US
dc.identifier.issn1099-0488en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38859
dc.description.abstractNormal mode analyses were done for the exact structures of model oligomers of PEO to investigate the longitudinal acoustic mode (LAM) in this helical polymer. It quickly became apparent that it is impossible to reproduce observed LAM frequencies without incorporating explicit interchain interactions. We have developed a force field that includes interchain interactions through an atom-atom potential and have shown that this force field reproduces very well the observed LAM frequencies of helical-chain oligomers of PEO. This result indicates that the LAM of helical chains is much more sensitive to intermolecular interactions than that of planar zigzag chains.en_US
dc.format.extent883915 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherChemistryen_US
dc.subject.otherPolymer and Materials Scienceen_US
dc.titleRaman longitudinal acoustic mode (LAM) studies of folded-chain morphology in poly(ethylene oxide) (PEO). I. Normal mode analysis of LAM of a helical-chain oligomer of PEOen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMacromolecular Research Center and Department of Physics, The University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumMacromolecular Research Center and Department of Physics, The University of Michigan, Ann Arbor, Michigan 48109 ; Macromolecular Research Center and Department of Physics, The University of Michigan, Ann Arbor, Michigan 48109en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38859/1/090280103_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/polb.1990.090280103en_US
dc.identifier.sourceJournal of Polymer Science Part B: Polymer Physicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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