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dc.contributor.authorLee, YPen_US
dc.contributor.authorWu, YOen_US
dc.contributor.authorLees, RMen_US
dc.contributor.authorXu, LHen_US
dc.contributor.authorHougen, JTen_US
dc.date.accessioned2014-12-08T15:17:33Z-
dc.date.available2014-12-08T15:17:33Z-
dc.date.issued2006-01-20en_US
dc.identifier.issn0036-8075en_US
dc.identifier.urihttp://dx.doi.org/10.1126/science.1121300en_US
dc.identifier.urihttp://hdl.handle.net/11536/12725-
dc.description.abstractThe quantum solid para-hydrogen (p-H-2) has recently proven useful in matrix isolation spectroscopy. Spectral lines of compounds embedded in this host are unusually narrow, and several species have been reported to rotate in p-H-2. We found that a p-H-2 matrix inhibits rotation of isolated methanol (CH3OH) but still allows internal rotation about the C-O bond, with splittings of the E/A torsional doublet in internal rotation-coupled vibrational modes that are qualitatively consistent with those for CH3OH in the gaseous phase. This simplified high-resolution spectrum further revealed the slow conversion of nuclear spin symmetry from species E to species A in the host matrix, offering potential insight into nuclear spin conversion in astrophysical sources.en_US
dc.language.isoen_USen_US
dc.titleInternal rotation and spin conversion of CH3OH in solid para-hydrogenen_US
dc.typeArticleen_US
dc.identifier.doi10.1126/science.1121300en_US
dc.identifier.journalSCIENCEen_US
dc.citation.volume311en_US
dc.citation.issue5759en_US
dc.citation.spage365en_US
dc.citation.epage368en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000234938500040-
dc.citation.woscount45-
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