4.8 Article

Exciton Trapping Dynamics in DNA Multimers

期刊

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 10, 期 7, 页码 1639-1643

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.9b00450

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资金

  1. LASERLAB-EUROPE (H2020) [654148]
  2. European Research Council [291198]
  3. ETN LightDyNAmics [765266]
  4. European Research Council (ERC) [291198] Funding Source: European Research Council (ERC)

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Using as a model the single adenine strand (dA)(20), we study the ultrafast evolution of electronic excitations in DNA with a time resolution of 30 fs. Our transient absorption spectra in the UV and visible spectral domains show that internal conversion among photogenerated exciton states occurs within 100 fs. Subsequently, the pi pi* states acquire progressively charge-transfer character before being completely trapped, within 3 ps, by fully developed charge-transfer states corresponding to transfer of an electron from one adenine moiety to another (A(+)A(-)).

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