Temperature effects on the internal conversion of excited adenine and adenosine

被引:0
|
作者
Mansour, Ritam [1 ]
Toldo, Josene M. [1 ]
Mukherjee, Saikat [1 ]
Pinheiro Jr, Max
Barbatti, Mario [1 ,2 ]
机构
[1] Aix Marseille Univ, CNRS, ICR, Marseille, France
[2] Inst Univ France, F-75231 Paris, France
基金
欧盟地平线“2020”; 欧洲研究理事会;
关键词
STATE DEACTIVATION; POLARIZATION PROPAGATOR; PERTURBATION-THEORY; DYNAMICS; SIMULATION; MECHANISM; CLUSTERS; SPECTRA; SCHEME;
D O I
10.1039/D3CP03234E
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This work aims to elucidate the dependence of the excited-state lifetime of adenine and adenosine on temperature. So far, it has been experimentally shown that while adenine's lifetime is unaffected by temperature, adenosine's lifetime strongly depends on it. However, the non-Arrhenius temperature dependence has posed a challenge in explaining this phenomenon. We used surface hopping to simulate the dynamics of adenine and adenosine in the gas phase at 0 and 400 K. The temperature effects were observed under the initial conditions via Wigner sampling with thermal corrections. Our results confirm that adenine's excited-state lifetime does not depend on temperature, while adenosine's lifetime does. Adenosine's dependency is due to intramolecular vibrational energy transfer from adenine to the ribose group. At 0 K, this transfer reduced the mean kinetic energy of adenine's moiety so much that internal conversion is inhibited, and the lifetime elongated by a factor of 2.3 compared to that at 400 K. The modeling also definitively ruled out the influence of viscosity, which was proposed as an alternative explanation previously. Temperature has a strikingly different impact on adenine and adenosine photodynamics. Surface hopping reveals the reason underlying it.
引用
收藏
页码:27083 / 27093
页数:11
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