Dynamics of H-atom loss in adenine

Literature Information

Publication Date 2004-10-05
DOI 10.1039/B411295D
Impact Factor 3.676
Authors


View Original

Abstract

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.

Related Literature

Novel polymer nanocomposites from bioinspired green aqueous functionalization of BNNTs

Vijay Kumar Thakur, Jian Yan, Meng-Fang Lin, Chunyi Zhi, Dmitri Golberg, Yoshio Bando, Raymond Sim

2012-01-31 Paper

DOI: 10.1039/C2PY00612J

One-step RAFT synthesis of well-defined amphiphilic star polymers and their self-assembly in aqueous solution

Christoph Herfurth, Paula Malo de Molina, Christoph Wieland, Sarah Rogers, Michael Gradzielski

2012-04-26 Paper

DOI: 10.1039/C2PY20126G

Molecular design, synthesis and characterization of aromatic polythioester and polydithioester

Daisuke Abe, Yuji Sasanuma

2012-04-03 Paper

DOI: 10.1039/C2PY20118F

A new polyfluorene bearing pyridine moieties: a sensitive fluorescent chemosensor for metal ions and cyanide

Xiaoding Lou, Yi Zhang, Shuang Li, Daxin Ou, Zhaomin Wan, Jingui Qin, Zhen Li

2012-04-03 Paper

DOI: 10.1039/C2PY20022H

Contents list

Front/Back Matter

DOI: 10.1039/C2PY90012B

Poly(ethylene) brushes grafted to silicon substrates

Denis Damiron, Jérôme Mazzolini, Fabrice Cousin, Christophe Boisson, Franck D'Agosto, Eric Drockenmuller

2011-11-24 Paper

DOI: 10.1039/C1PY00459J

Functional conjugated microporous polymers: from 1,3,5-benzene to 1,3,5-triazine

Shijie Ren, Robert Dawson, Andrea Laybourn, Jia-xing Jiang, Yaroslav Khimyak, Dave J. Adams, Andrew I. Cooper

2012-01-30 Paper

DOI: 10.1039/C2PY00585A

Organoboron star polymersvia arm-first RAFT polymerization: synthesis, luminescent behavior, and aqueous self-assembly

Fei Cheng, Edward M. Bonder, Ami Doshi, Frieder Jäkle

2012-01-03 Communication

DOI: 10.1039/C2PY00556E

Poly(dopamine acrylamide)-co-poly(propargyl acrylamide)-modified titanium surfaces for ‘click’ functionalization

Li Qun Xu, Hua Jiang, Koon-Gee Neoh, En-Tang Kang, Guo Dong Fu

2012-01-30 Paper

DOI: 10.1039/C2PY00552B

Substituent effects on the stabilities of polymeric and small molecule bis-terpyridine complexes

Ian M. Henderson, Ryan C. Hayward

2012-03-13 Paper

DOI: 10.1039/C2PY20042B

You might also like

Compound Q&A

Are there alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3848-36-0) in synthesis?

When considering alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3...

3848-36-01-(4-Chlorophenyl)-N...
Compound Q&A

How is 3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole (CAS: 419553-16-5) typically synthesized?

3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole is synthesized through a m...

419553-16-53-(4-Bromophenyl)-5-...
Compound Q&A

How is 5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS: 1639220-19-1) typically synthesized?

5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS...

1639220-19-15-Chloro-2-(4-chloro...
Compound Q&A

What industries use 2-Chloro-4-(difluoromethoxy)pyridine (CAS: 1206978-15-5)?

2-Chloro-4-(difluoromethoxy)pyridine is used in the pharmaceutical industry for ...

1206978-15-52-Chloro-4-(difluoro...
Compound Q&A

What regulatory guidelines apply to 3-Chloro-6-methylpyridazine (CAS: 1121-79-5)?

3-Chloro-6-methylpyridazine (CAS: 1121-79-5) is classified under the Globally Ha...

1121-79-53-Chloro-6-methylpyr...
Compound Q&A

Are there alternatives to Methyl 4,5-dimethyl-2-nitrobenzoate in synthesis?

Several alternatives can be used in the synthesis of Methyl 4,5-dimethyl-2-nitro...

90922-74-0Methyl 4,5-dimethyl-...
Compound Q&A

Are there alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde in synthesis?

Alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde include other acry...

63405-68-5(2E,2'E)-3,3'-(1,4-P...
Compound Q&A

What is 3-Amino-5-chloropyridin-2-ol hydrochloride (CAS: 1261906-29-9)?

3-Amino-5-chloropyridin-2-ol hydrochloride is an organic compound with the CAS n...

1261906-29-93-Amino-5-chloropyri...
Compound Q&A

What precautions should be taken when handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one (CAS: 1092349-93-3)?

When handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one, it is essential to wear...

1092349-93-36,7-Difluoro-2,3-dih...

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 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.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.