Ultrafast IR spectroscopy of polymeric cytosine nucleic acids reveal the long-lived species is due to a localised state-Reference-Cited by-同舟云学术

Ultrafast IR spectroscopy of polymeric cytosine nucleic acids reveal the long-lived species is due to a localised state

Published:2012 Issue:18 Volume:14 Page:6307
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Keane Páraic M.,Wojdyla Michal,Doorley Gerard W.,Kelly John M.,Clark Ian P.,Parker Anthony W.,Greetham Gregory M.,Towrie Michael,Magno Luís M.,Quinn Susan J.

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2012/CP/C2CP23774A

Reference22 articles.

1. DNA Excited-State Dynamics: From Single Bases to the Double Helix

2. Fluorescence of DNA Duplexes: From Model Helices to Natural DNA

3. Exciting DNA

4. Internal conversion to the electronic ground state occurs via two distinct pathways for pyrimidine bases in aqueous solution

5. Ultrafast IR spectroscopy of the short-lived transients formed by UV excitation of cytosine derivatives

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unraveling Excited State Dynamics of a Single-Stranded DNA-Assembled Conjugated Polyelectrolyte;The Journal of Physical Chemistry Letters;2023-10-26

2. The photophysics of protonated cytidine and hemiprotonated cytidine base pair: A computational study;Photochemistry and Photobiology;2023-07-06

3. Ultrafast Electronic Relaxation in 6-Methyluracil and 5-Fluorouracil in Isolated and Aqueous Conditions: Substituent and Solvent Effects;The Journal of Physical Chemistry Letters;2023-03-10

4. Ultrafast excited state dynamics of silver ion-mediated cytosine–cytosine base pairs in metallo-DNA;The Journal of Chemical Physics;2020-09-14

5. The influence of loops on the binding of the [Ru(phen)2dppz]2+ light-switch compound to i-motif DNA structures revealed by time-resolved spectroscopy;Chemical Communications;2020