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dc.contributor.authorUsman, Anwaren_US
dc.contributor.authorAsahi, Tsuyoshien_US
dc.contributor.authorSugiyama, Terukien_US
dc.contributor.authorMasuhara, Hiroshien_US
dc.contributor.authorTohnai, Norimitsuen_US
dc.contributor.authorMiyata, Mikijien_US
dc.date.accessioned2014-12-08T15:47:44Z-
dc.date.available2014-12-08T15:47:44Z-
dc.date.issued2010-11-18en_US
dc.identifier.issn1520-6106en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jp909850ren_US
dc.identifier.urihttp://hdl.handle.net/11536/31923-
dc.description.abstractWe have studied the photochromic reaction of p-hydroxycinnamic-thiophenyl ester in the microcrystalline state We attributed the fluorescence spectral evolution of the microcrystal under UV irradiation to the photoinduced trans-to-cis isomerization The photocyclic behavior of the chromophore was demonstrated by cis-to-trans back reaction under a subsequent visible light irradiation In addition the [2 2] topochemical photocyclodimer was observed as another photoproduct It is considered that the cooperative photoisomerization is initiated at the local lattice distortion and free spaces around the [2 + 2] cyclodimer near the crystal sui lace and the photoisomerization induces larger lattice deformation and further photoisomerization in the interior of the crystalen_US
dc.language.isoen_USen_US
dc.titlePhotochemical Reaction of p-hydroxycinnamic-thiophenyl Ester in the Microcrystalline Stateen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jp909850ren_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Ben_US
dc.citation.volume114en_US
dc.citation.issue45en_US
dc.citation.spage14233en_US
dc.citation.epage14240en_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
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