Back to Search Start Over

Effect of Ag+ on the Excited-State Properties of a Gas-Phase (Cytosine)2Ag+ Complex: Electronic Transition and Estimated Lifetime

Authors :
Claude Dedonder-Lardeux
Géraldine Féraud
Matias Berdakin
Gustavo A. Pino
Christophe Jouvet
Instituto de Investigaciones en Físico Química [Córdoba] (INFIQC)
Consejo Nacional de Investigaciones Científicas y Técnicas [Buenos Aires] (CONICET)-Facultad de Ciencias Químicas [Córdoba]
Universidad Nacional de Córdoba [Argentina]-Universidad Nacional de Córdoba [Argentina]
Physique des interactions ioniques et moléculaires (PIIM)
Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)
ECOS-MinCyT cooperation program (A11E02)
ANR-10-BLAN-0405,ESPM,Etats excités des molécules protonées(2010)
Source :
CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET, Journal of Physical Chemistry Letters, Journal of Physical Chemistry Letters, American Chemical Society, 2014, 5, 2295-2301 Reprinted (adapted) with permission from Journal of Physical Chemistry Letters. ⟨10.1021/jz5009455⟩, Journal of Physical Chemistry Letters, 2014, 5, 2295-2301 Reprinted (adapted) with permission from Journal of Physical Chemistry Letters. ⟨10.1021/jz5009455⟩
Publication Year :
2014
Publisher :
American Chemical Society (ACS), 2014.

Abstract

Recently, DNA molecules have received great attention because of their potential applications in material science. One interesting example is the production of highly fluorescent and tunable DNA–Agn clusters with cytosine (C)-rich DNA strands. Here, we report the UV photofragmentation spectra of gas-phase cytosine···Ag+···cytosine (C2Ag+) and cytosine···H+···cytosine (C2H+) complexes together with theoretical calculations. In both cases, the excitation energy does not differ significantly from that of isolated cytosine or protonated cytosine, indicating that the excitation takes place on the DNA base. However, the excited-state lifetime of the C2H+ (τ = 85 fs), estimated from the bandwidth of the spectrum, is at least 2 orders of magnitude shorter than that of the C2Ag+ (τ > 5000 fs). The increased excited-state lifetime upon silver complexation is quite unexpected, and it clearly opens the question about what factors are controlling the nonradiative decay in pyrimidine DNA bases. This is an important result for the expanding field of metal-mediated base pairing and may also be important to the photophysical properties of DNA-templated fluorescent silver clusters. Fil: Berdakin, Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina Fil: Féraud, Geraldine. Aix Marseille Université. Marsella; Francia Fil: Dedonder Lardeux, Claude. Aix Marseille Université. Marsella; Francia Fil: Jouvet, Christophe. Aix Marseille Université. Marsella; Francia Fil: Pino, Gustavo Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina

Details

ISSN :
19487185
Volume :
5
Database :
OpenAIRE
Journal :
The Journal of Physical Chemistry Letters
Accession number :
edsair.doi.dedup.....2336f054752e3128bf1386072a765788
Full Text :
https://doi.org/10.1021/jz5009455