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Journal

2011 | 9 | 3 | 792-799

Article title

Excited-state hydrogen bonding dynamics of methyl isocyanide in methanol solvent: A DFT/TDDFT study

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EN

Abstracts

EN
The time-dependent density functional theory (TDDFT) method was performed to investigate the hydrogenbonding dynamics of methyl cyanide (MeNC) as hydrogen bond acceptor in hydrogen donating methanol (MeOH) solvent. The ground-state geometry optimizations and electronic transition energies and corresponding oscillation strengths of the low-lying electronically excited states for the isolated MeNC and MeOH monomers, the hydrogen-bonded MeNC-MeOH dimer and MeNC-2MeOH trimer are calculated by the DFT and TDDFT methods, respectively. An intermolecular hydrogen bond N≡C…H-O is formed between MeNC and methanol molecule. According to Zhao’s rule on the excited-state hydrogen bonding dynamics, we find the intermolecular hydrogen bonds N≡C…H-O are strengthened in electronically excited states of the hydrogen-bonded MeNC-MeOH dimer and MeNC-2MeOH trimer, with the excitation energy of a related excited state being lowered and electronic spectral redshifts being induced. Furthermore, the hydrogen bond strengthening in the electronically excited state plays an important role on the photophysics and photochemistry of MeNC in solutions

Publisher

Journal

Year

Volume

9

Issue

3

Pages

792-799

Physical description

Dates

published
1 - 6 - 2011
online
26 - 2 - 2011

Contributors

author
  • School of Physics, Ludong University, Yantai, 264025, China
author
  • School of Physics, Ludong University, Yantai, 264025, China
author
  • College of Mechanical and Electronic Engineering, Hebei University of Science and Technology, Shijiazhuang, 050054, China
author
  • College of Mechanical and Electronic Engineering, Hebei University of Science and Technology, Shijiazhuang, 050054, China
author
  • School of Physics, Ludong University, Yantai, 264025, China

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bwmeta1.element.-psjd-doi-10_2478_s11534-010-0099-4
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