2001The Journal of Physical Chemistry ARequires access

On the Photochemistry of Purine Nucleobases

Eyal Nir, Karl Kleinermanns, Louis Grace, Mattanjah S. de Vries

Open publisher page 172 citations

Abstract

We present R2PI spectra of a series of purine nucleobases, nucleosides, and related derivatives, including adenine, guanine, guanosine, 2-aminopurine, 2,6-diaminopurine, 9-ethyladenine, and 9-methylguanine. We compare the results with models involving two interacting excited states, which have been proposed to explain the short excited-state lifetime of most nucleobases. The amino group in the 2 position appears to have a strong effect on the excited-state potentials, as does any substitution in the 9 position. This explains the very different fluorescence characteristics of 2-aminopurine, but it raises new questions concerning the short lifetime of guanine in solution.

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What this paper is about

We present R2PI spectra of a series of purine nucleobases, nucleosides, and related derivatives, including adenine, guanine, guanosine, 2-aminopurine, 2,6-diaminopurine, 9-ethyladenine, and 9-methylguanine. We compare the results with models involving two interacting excited states, which have been proposed to explain the short excited-state lifetime of most nucleobases. The amino group in the 2 position appears to have a strong effect on the excited-state potentials, as does any substitution in the 9 position. This explains the very different fluorescence characteristics of 2-aminopurine, but it raises new questions concerning the short lifetime of guanine in solution.

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Available abstract

We present R2PI spectra of a series of purine nucleobases, nucleosides, and related derivatives, including adenine, guanine, guanosine, 2-aminopurine, 2,6-diaminopurine, 9-ethyladenine, and 9-methylguanine. We compare the results with models involving two interacting excited states, which have been proposed to explain the short excited-state lifetime of most nucleobases. The amino group in the 2 position appears to have a strong effect on the excited-state potentials, as does any substitution in the 9 position. This explains the very different fluorescence characteristics of 2-aminopurine, but it raises new questions concerning the short lifetime of guanine in solution.

Key concepts: Nucleobase, Guanine, Excited state, Guanosine, Purine, Chemistry, Stereochemistry, Photochemistry

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