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dc.contributor.authorLiu, Bingguoen_US
dc.contributor.authorHe, Chunyuanen_US
dc.contributor.authorJin, Mingxingen_US
dc.contributor.authorWang, Qiaoqiaoen_US
dc.contributor.authorLin, Sheng Hsienen_US
dc.contributor.authorDing, Dajunen_US
dc.date.accessioned2014-12-08T15:07:09Z-
dc.date.available2014-12-08T15:07:09Z-
dc.date.issued2010-03-29en_US
dc.identifier.issn1094-4087en_US
dc.identifier.urihttp://dx.doi.org/10.1364/OE.18.006863en_US
dc.identifier.urihttp://hdl.handle.net/11536/5622-
dc.description.abstractEffects of high pressure in a range of up to 1.7 GPa on ultrafast energy relaxation of LDS698 (C(19)H(23)N(2)O(4)Cl) molecules in solution have experimentally been illustrated by a method of femtosecond time-resolved absorption spectroscopy. The rates of the intramolecular and intermolecular energy relaxations show quite different pressure dependences. The observed results are in good agreement with the theoretical interpretation based on the pressure influences on the molecular energy gaps, the intermolecular H-bond interaction, and the solution viscosity. (C) 2010 Optical Society of Americaen_US
dc.language.isoen_USen_US
dc.titleHigh pressure effect on the ultrafast energy relaxation rate of LDS698 (C(19)H(23)N(2)O(4)Cl) in a solutionen_US
dc.typeArticleen_US
dc.identifier.doi10.1364/OE.18.006863en_US
dc.identifier.journalOPTICS EXPRESSen_US
dc.citation.volume18en_US
dc.citation.issue7en_US
dc.citation.spage6863en_US
dc.citation.epage6870en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
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