Propiolic Acid in Solid Nitrogen: NIR- and UV-Induced cis → trans Isomerization and Matrix-Site-Dependent trans → cis Tunneling

Lopes S., Nikitin T., Fausto R.

JOURNAL OF PHYSICAL CHEMISTRY A, vol.123, no.8, pp.1581-1593, 2019 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 123 Issue: 8
  • Publication Date: 2019
  • Doi Number: 10.1021/acs.jpca.8b11319
  • Journal Name: JOURNAL OF PHYSICAL CHEMISTRY A
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.1581-1593
  • Istanbul Kültür University Affiliated: Yes

Abstract

Propiolic acid(HCCCOOH, PA) was studied experimentally by infrared spectroscopy in a nitrogen matrix and by ab initio calculations. The vibrational spectra of the cis and trans monomers(O=C-O-H dihedral equal to 0 and 180 degrees, respectively) were measured and assigned. The trans-PA monomer was produced by selective vibrational excitation of the cis-PA monomer molecules trapped in different matrix sites. Broadband in situ UV irradiation(lambda > 235 nm) of matrix-isolated PA yielded as product the higher-energy trans conformer, with no other photo products being detected. Two cis-cis dimers were also identified in the matrixes and characterized structurally and vibrationally. trans- PA was found to decay back to cis-PA in the dark, by tunneling, and the different lifetimes of the higher-energy PA conformer resulting from pumping different matrix sites and different experimental conditions (using a filter blocking the higher-energy IR radiation of the spectrometer source and without using such a filter) were discussed.