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dc.contributor.authorLin, LR
dc.contributor.author林丽榕
dc.contributor.authorChen, H
dc.contributor.authorChen, MD
dc.contributor.authorJiang, YB
dc.contributor.author江云宝
dc.contributor.authorHuang, XZ
dc.contributor.authorChen, GZ
dc.date.accessioned2012-07-08T03:37:19Z
dc.date.available2012-07-08T03:37:19Z
dc.date.issued1999
dc.identifier.citationCHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1999,20(9):1358-1361zh_CN
dc.identifier.issn0251-0790
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/13181
dc.description.abstractDual fluorescence of a series of p-dialkylaminobenzoic acids in non-polar solvent,l-hexane was observed. Picosecond time-resolved fluorescence and solvent polarity effect experiments demonstrated that the dual fluorescence is due to the excited state intramolecular charge transfer that produces the emissive charge transfer state in addition to the locally excited state, Dynamics data from the time-resolved fluorescence measurements indicated that the observation of the intramolecular charge transfer of p-dialkylaminobenzoic acids in nonpolar solvent is due to the low activation energy for the charge transfer process.zh_CN
dc.language.isozhzh_CN
dc.publisherHIGHER EDUCATION PRESSzh_CN
dc.subjectintramolecular charge transferzh_CN
dc.subjectdual fluorescencezh_CN
dc.subjectp-dialkylaminobenzoic acidzh_CN
dc.subjectnon-polar solventzh_CN
dc.titleIntramolecular charge transfer dual fluorescence of p-dialkylaminobenzoic acids in n-hexanezh_CN
dc.typeArticlezh_CN


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