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Watson, Graeme W.
Preferred name
Watson, Graeme W.
Official Name
Watson, Graeme W.
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Now showing 1 - 2 of 2
- PublicationTracking DNA excited states by picosecond-time-resolved infrared spectroscopy: Signature band for a charge-transfer excited state in stacked adenine-thymine systems(American Chemical Society, 2013-07-29)
; ; ; ; UV photoexcitation of an adenine-thymine heterodimer (ApT) in D 2O yields a complex transient infrared signature in the 1500-1600 cm-1 spectral region. The spectral dynamics fit well to a biexponential decay assignable to two transient species. The first, a short-lived species with a lifetime of ca. 5 ps, originates from the vibrationally hot electronic ground state of the unstacked form of the dinucleotide. The second species is longer-lived (ca. 75 ps), and its yield correlates to the amount of stacked dinucleotide present in solution. We assign the longer-lived component to a charge-transfer (A•+pT •-) state by comparison with calculated spectra for the adenine radical cation and thymine radical anion. Significantly, the CT feature is also identified in UV-excited [poly(dA-dT)]2. This experimental observation gives a powerful insight into how base-base interactions lead to extended-lifetime electronic excited states of the nucleic acid bases and how a dimeric structure controls the relaxation pathway. © 2013 American Chemical Society.Scopus© Citations 74 261 - PublicationA comparative picosecond transient infrared study of 1-methylcytosine and 5'-dCMP that sheds further light on the excited states of cytosine derivatives(ACS Publications, 2011-03)
; ; ; ; ; ; ; ; ; The role of N1-substitution in controlling the deactivation processes in photoexcited cytosine derivatives has been explored using picosecond time-resolved IR spectroscopy. The simplest N1-substituted derivative, 1-methylcytosine, exhibits relaxation dynamics similar to the cytosine nucleobase and distinct from the biologically relevant nucleotide and nucleoside analogues, which have longer-lived excited-state intermediates. It is suggested that this is the case because the sugar group either facilitates access to the long-lived (1)n(O)Ï * state or retards its crossover to the ground state.Scopus© Citations 47 484