Photoisomerization and Photochemistry of Matrix-Isolated 3-Furaldehyde

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KUŞ N., Reva I., Fausto R.

JOURNAL OF PHYSICAL CHEMISTRY A, vol.114, no.47, pp.12427-12436, 2010 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 114 Issue: 47
  • Publication Date: 2010
  • Doi Number: 10.1021/jp1079839
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.12427-12436
  • Anadolu University Affiliated: Yes


3-Furaldehyde (3FA) was isolated in an argon matrix at 12 K and studied using FTIR spectroscopy and quantum chemistry The molecule has two conformers with trans and cis orientation of the O=C-C=C dihedral angle At the B3LYP/6-311++G(d p) level of theory, the trans form was computed to beer 4 kJ mol(-1) more stable than the cis form The relative stability of the two conformers was explained using the natural bond orbital (NBO) method In fair agreement with their calculated relative energies and the high barrier of rotamerization (ca 34 kJ mol(-1) from trans to cis) the trans and cis con formers were trapped in an argon matrix from the compound room temperature gas phase in proportion similar to 7 1 The experimentally observed vibrational signatures of the two forms are in a good agreement with the theoretically calculated spectra Broad-band UV-irradiation (lambda > 234 nm) of the matrix-isolated compound resulted in partial trans - cis isomerization which ended at a photostationary state with the trans/cis ratio being ca 1 85 1 This result was interpreted based on results of time-dependent OFT calculations Irradiation at higher energies (lambda > 200 nm) led to decarbonylation of the compound yielding furan cyclopropene-3-carbaldehyde and two C3H4 isomers cyclopropene and propadiene