Theoretical study of the structures, conformations, and spectroscopic properties of 2-Formylthiophene-N-acetylhydrazone and 2-thiophenecarboxaldehyde- 2-thienylhydrazone

2-Formylthiophene-N-acetylhydrazone (Hait) and 2-thiophenecarboxaldehyde-2-thienylhydrazone (Htit) in the cis and trans conformations were investigated in the gas-phase by density functional method using B3LYP as the functional set and 6-311++G(d,p) as the basis set. The cis and trans structures were fully optimized in the C1 and Cs symmetries. Transition states were also modeled for the cis–trans isomerization of the title compounds and the barriers to internal rotation were calculated. This work reports the structural, energetics, and spectroscopic parameters of all the optimized geometries. Some of the structural parameters are in good agreement with experimental literature data. The computed parameters for these compounds are also in good agreement with a related molecule, namely, acetohydrazide. For both Hait and Htit, the trans conformers are more stable than the cis conformers and the energy barriers are larger compared with the energy differences between the cis and trans conformers. This accounts for Hait and Htit existing mostly in the trans conformation. © 2009 Wiley Periodicals, Inc. Heteroatom Chem 20:144–150, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20526