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dc.contributor.advisorKohler, Bern
dc.creatorMiddleton, Chris
dc.date.accessioned2008-06-04T22:34:44Z
dc.date.available2008-06-04T22:34:44Z
dc.date.issued2008-04
dc.identifier.citationPatrick M. Hare, Chris T. Middleton, Kristin I. Mertel, John M. Herbert, and Bern Kohler, Chemical Physics (2008), 347, 383-392.en_US
dc.identifier.urihttp://hdl.handle.net/1811/32193
dc.descriptionMathematical and Physical Sciences: 3rd Place (The Ohio State University Edward F. Hayes Graduate Research Forum)en_US
dc.description.abstractTo better understand the link between light absorption and deleterious DNA photoproducts, the photophysics of DNA bases was investigate with femtosecond mid-IR transient absorption spectroscopy. Markers band for two excited states, a dark singlet state and a triplet state, were found. These marker bands provide insight into the nature and dynamics of the states. The results confirm a model for pyrimidine bases previous proposed based on UV-visible transient absorption measurements. This study provides an important foundation for future investigations of the role of these states in DNA.en_US
dc.language.isoenen_US
dc.relation.ispartofseries2008 Edward F. Hayes Graduate Research Forum. 22nden_US
dc.subjectDNA photophysicsen_US
dc.subjecttime-resolved spectroscopyen_US
dc.subjectexcited-state dynamicsen_US
dc.subjecttime-resolved infrareden_US
dc.titleExcited-State Dynamics of Pyrimidine DNA Bases Revealed by Ultrafast Vibrational Spectroscopyen_US
dc.typeArticleen_US
dc.description.embargoA five-year embargo was granted for this item.en_US


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