Literature DB >> 15634133

The triplet state of cytosine and its derivatives: electron impact and quantum chemical study.

Robert Abouaf1, Jacqueline Pommier, Henri Dunet, Phung Quan, Pham-Cam Nam, Minh Tho Nguyen.   

Abstract

The excitation of the lowest electronic states and vibrational excitation of cytosine (C) have been studied using electron energy loss spectroscopy (EELS, 0-100 eV) with angular analysis. The singlet states have been found to be in good agreement with UV-VIS absorption results on sublimed films, slightly blueshifted by about 0.1 eV. The EEL spectra recorded at residual energy below 2 eV show clear shoulders at energy losses of 3.50 and 4.25 eV (+/-0.1 eV). They are assigned to the lowest triplet electronic states of cytosine. Energies and molecular structures of the lowest-lying triplet state of C and its methylated and halogenated 5-X-C, 6-X-C, and 5-X, 6-X-C substituted derivatives (X=CH3, F, Cl, and Br) have been studied using quantum chemical calculations with both molecular orbital and density functional methods, in conjunction with the 6-311++G(d,p), 6-311++G(3df,2p), and aug-cc-pVTZ basis sets. The triplet-singlet energy gap obtained using coupled-cluster theory [CCSD(T)] and density functional theory (DFT) methods agrees well with those derived from EELS study. The first C's vertical triplet state is located at 3.6 eV, in good agreement with experiment. The weak band observed at 4.25 eV is tentatively assigned to the second C's vertical triplet excitation. For the substituted cytosines considered, the vertical triplet state is consistently centered at 3.0-3.2 eV above the corresponding singlet ground state but about 1.0 eV below the first excited singlet state. Geometrical relaxation involving out-of-plane distortions of hydrogen atoms leads to a stabilization of 0.6-1.0 eV in favor of the equilibrium triplet. The lowest-lying adiabatic triplet states are located at 2.3-3.0 eV. Halogen substitution at both C(5) and C(6) positions tends to reduce the triplet-singlet separations whereas methylation tends to enlarge it. The vibrational modes of triplet cytosine and the ionization energies of substituted derivatives were also evaluated. (c) 2004 American Institute of Physics

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Year:  2004        PMID: 15634133     DOI: 10.1063/1.1812533

Source DB:  PubMed          Journal:  J Chem Phys        ISSN: 0021-9606            Impact factor:   3.488


  5 in total

1.  DFT and MP2 investigations of L-proline and its hydrated complexes.

Authors:  Xiao-Jun Li; Zhi-Jian Zhong; Hai-Zhen Wu
Journal:  J Mol Model       Date:  2011-01-25       Impact factor: 1.810

2.  Measurement of inelastic cross sections for low-energy electron scattering from DNA bases.

Authors:  Marc Michaud; Marc Bazin; Léon Sanche
Journal:  Int J Radiat Biol       Date:  2011-05-26       Impact factor: 2.694

3.  Absolute cross sections for vibrational excitations of cytosine by low energy electron impact.

Authors:  M Michaud; M Bazin; L Sanche
Journal:  J Chem Phys       Date:  2012-09-21       Impact factor: 3.488

4.  Absolute cross sections for electronic excitations of cytosine by low energy electron impact.

Authors:  M Bazin; M Michaud; L Sanche
Journal:  J Chem Phys       Date:  2010-10-21       Impact factor: 3.488

5.  Time-resolved cathodoluminescence of DNA triggered by picosecond electron bunches.

Authors:  Jean Philippe Renault; Bruno Lucas; Thomas Gustavsson; Alain Huetz; Thomas Oksenhendler; Elena-Magdalena Staicu-Casagrande; Marie Géléoc
Journal:  Sci Rep       Date:  2020-03-19       Impact factor: 4.379

  5 in total

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