Dynamics of H-atom loss in adenine

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发布日期 2004-10-05
DOI 10.1039/B411295D
影响因子 3.676
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摘要

Time- and frequency resolved detection of H-atoms was used to investigate the excited-state photophysics and photochemistry of isolated adenine and 9-methyladenine at two excitation wavelengths, 266 nm and 239.5 nm. By comparison of the two molecules it is shown that dissociation of the N9–H bond is an important deactivation pathway in adenine. The appearance time of the H-atoms was shorter than a few nanoseconds, indicating a rapid non-statistical dissociation. From the Doppler profiles a dissociation energy of 393 ± 20 kJ mol−1 was determined for adenine. Typically 40–50% of the excess energy is released as translation. The Doppler profile of the H-atom photofragments from adenine excited at 239.5 nm shows an anisotropic angular distribution and suggests that dissociation occurs in less than a rotational period. An anisotropy parameter β ≈ −0.9 was derived, indicating an almost pure perpendicular transition. Our data are consistent with a H-atom loss in adenine that can be adequately described by a coupling with πσ* excited states as recently suggested in the literature. The Doppler profiles of 9-methyladenine on the other hand are more isotropic. From the width of the profile it is assumed that not only one of the N–H bonds in the amino group is cleaved, but some H-loss also occurs on the methyl group.

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来源期刊

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
自引率: 10.3%
年发文量: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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