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Solvent structural relaxation dynamics in dipolar solvation studied by resonant pump polarizability response spectroscopy

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dc.contributor.authorPark, Sungnam-
dc.contributor.authorKim, Jeongho-
dc.contributor.authorMoran, Andrew M.-
dc.contributor.authorScherer, Norbert F.-
dc.date.accessioned2021-09-07T21:55:29Z-
dc.date.available2021-09-07T21:55:29Z-
dc.date.issued2011-
dc.identifier.issn1463-9076-
dc.identifier.issn1463-9084-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/115039-
dc.description.abstractResonant pump polarizability response spectroscopy (RP-PORS) was used to study the isotropic and anisotropic solvent structural relaxation in solvation. RP-PORS is the optical heterodyne detected transient grating (OHD-TG) spectroscopy with an additional resonant pump pulse. A resonant pump excites the solute-solvent system and the subsequent relaxation of the solute-solvent system is monitored by the OHD-TG spectroscopy. This experimental method allows measuring the dispersive and absorptive parts of the signal as well as fully controlling the beam polarizations of incident pulses and signal. The experimental details of RP-PORS were described. By performing RP-PORS with Coumarin 153(C153) in CH3CN and CHCl3, we have successfully measured the isotropic and anisotropic solvation polarizability spectra following electronic excitation of C153. The isotropic solvation polarizability responses result from the isotropic solvent structural relaxation of the solvent around the solute whereas the anisotropic solvation polarizability responses come from the anisotropic translational relaxation and orientational relaxation. The solvation polarizability responses were found to be solvent-specific. The intramolecular vibrations of CHCl3 were also found to be coupled to the electronic excitation of C153.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleSolvent structural relaxation dynamics in dipolar solvation studied by resonant pump polarizability response spectroscopy-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/c0cp01252a-
dc.identifier.scopusid2-s2.0-78650158152-
dc.identifier.wosid000285099800025-
dc.identifier.bibliographicCitationPHYSICAL CHEMISTRY CHEMICAL PHYSICS, v.13, no.1, pp 214 - 223-
dc.citation.titlePHYSICAL CHEMISTRY CHEMICAL PHYSICS-
dc.citation.volume13-
dc.citation.number1-
dc.citation.startPage214-
dc.citation.endPage223-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryPhysics, Atomic, Molecular & Chemical-
dc.subject.keywordPlusTRANSIENT-GRATING SPECTROSCOPY-
dc.subject.keywordPlusSTIMULATED RAMAN-SPECTROSCOPY-
dc.subject.keywordPlusDIFFRACTIVE OPTICS-
dc.subject.keywordPlusINTERMOLECULAR DYNAMICS-
dc.subject.keywordPlusVIBRATIONAL DYNAMICS-
dc.subject.keywordPlusPROBE SPECTROSCOPY-
dc.subject.keywordPlusEXCITED-STATE-
dc.subject.keywordPlusSTOKES SHIFT-
dc.subject.keywordPlusPHOTON-ECHO-
dc.subject.keywordPlusFEMTOSECOND-
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