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

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dc.contributor.authorPark, Sungnamko
dc.contributor.authorKim, Jeonghoko
dc.contributor.authorMoran, Andrew M.ko
dc.contributor.authorScherer, Norbert F.ko
dc.date.accessioned2013-03-08T22:58:37Z-
dc.date.available2013-03-08T22:58:37Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2011-
dc.identifier.citationPHYSICAL CHEMISTRY CHEMICAL PHYSICS, v.13, no.1, pp.214 - 223-
dc.identifier.issn1463-9076-
dc.identifier.urihttp://hdl.handle.net/10203/94581-
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 CH(3)CN and CHCl(3), 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 CHCl(3) were also found to be coupled to the electronic excitation of C153.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectSTIMULATED RAMAN-SPECTROSCOPY-
dc.subjectTRANSIENT-GRATING SPECTROSCOPY-
dc.subjectOPTICAL HETERODYNE-DETECTION-
dc.subjectDIFFRACTIVE OPTICS-
dc.subjectINTERMOLECULAR DYNAMICS-
dc.subjectVIBRATIONAL DYNAMICS-
dc.subjectPROBE SPECTROSCOPY-
dc.subjectPOLAR-SOLVENTS-
dc.subjectEXCITED-STATE-
dc.subjectBETA-CAROTENE-
dc.titleSolvent structural relaxation dynamics in dipolar solvation studied by resonant pump polarizability response spectroscopy-
dc.typeArticle-
dc.identifier.wosid000285099800025-
dc.identifier.scopusid2-s2.0-78650158152-
dc.type.rimsART-
dc.citation.volume13-
dc.citation.issue1-
dc.citation.beginningpage214-
dc.citation.endingpage223-
dc.citation.publicationnamePHYSICAL CHEMISTRY CHEMICAL PHYSICS-
dc.identifier.doi10.1039/c0cp01252a-
dc.contributor.localauthorKim, Jeongho-
dc.contributor.nonIdAuthorPark, Sungnam-
dc.contributor.nonIdAuthorMoran, Andrew M.-
dc.contributor.nonIdAuthorScherer, Norbert F.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusSTIMULATED RAMAN-SPECTROSCOPY-
dc.subject.keywordPlusTRANSIENT-GRATING SPECTROSCOPY-
dc.subject.keywordPlusOPTICAL HETERODYNE-DETECTION-
dc.subject.keywordPlusDIFFRACTIVE OPTICS-
dc.subject.keywordPlusINTERMOLECULAR DYNAMICS-
dc.subject.keywordPlusVIBRATIONAL DYNAMICS-
dc.subject.keywordPlusPROBE SPECTROSCOPY-
dc.subject.keywordPlusPOLAR-SOLVENTS-
dc.subject.keywordPlusEXCITED-STATE-
dc.subject.keywordPlusBETA-CAROTENE-
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