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Title:Conformers Of Vanillic Acid: A Rotational Spectroscopic And Theoretical Study
Author(s):Al-Jabiri, Mohamad
Contributor(s):Jäger, Wolfgang
Subject(s):Structure determination
Abstract:Vanillic acid is produced in significant quantities in forest fires and is used as a biomass burning tracer for softwood and hardwood combustion events. Vanillic acid has also been found in secondary organic aerosol and can be oxidized in aqueous atmospheric processes to humic-like substances. Hydrates of vanillic acid play undoubtedly important roles in the processes involved, and we present here a study of conformers of the vanillic acid monomer to lay the groundwork for subsequent studies of the mono- and di-hydrates. Computationally, 12 conformers were found within an energy range of 51 kJ/mol using the Conformer–Rotamer Ensemble Sampling Tool (CREST).$^1$ The two lowest energy conformers could then be identified in the spectrum recorded with a chirped pulse Fourier transform microwave spectrometer in the 2-6 GHz range. The deviation between experimental and theoretical rotational constants determined at the MP2/aug-cc-pVTZ and DFT B3LYP-D3(BJ)/def2-TVPZ levels of theory is less than 1\%. No tunnelling splitting was observed which suggests a relatively high barrier to methyl internal rotation, in agreement with other, previously studied vanillin derivatives. Furthermore, no c-type transitions could be observed in agreement with computed zero c-dipole moment component of the lowest energy structures. From the theoretical structures, it is apparent that intra-molecular hydrogen bonds play a significant role in stabilizing the lowest energy conformers. To further explore the intra-molecular interactions in vanillic acid, QTAIM and NCI analyses were performed. $^1$P. Pracht, F. Bohle, S. Grimme, Phys. Chem. Chem. Phys. 22, 7169-7192 (2020).
Issue Date:2021-06-24
Publisher:International Symposium on Molecular Spectroscopy
Genre:Conference Paper / Presentation
Date Available in IDEALS:2021-09-24

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