3-Iodobenzaldehyde: XRD, FT-IR, Raman and DFT studies

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
Chandraju Sadolalu Chidan KumarChing Kheng Quah

Abstract

The structure of 3-iodobenzaldehyde (3IB) was characterized by FT-IR, Raman and single-crystal X-ray diffraction techniques. The conformational isomers, optimized geometric parameters, normal mode frequencies and corresponding vibrational assignments of 3IB were examined using density functional theory (DFT) method, with the Becke-3-Lee-Yang-Parr (B3LYP) functional and the 6-311+G(3df,p) basis set for all atoms except for iodine. The LANL2DZ effective core basis set was used for iodine. Potential energy distribution (PED) analysis of normal modes was performed to identify characteristic frequencies. 3IB crystallizes in monoclinic space group P21/c with the O-trans form. There is a good agreement between the theoretically predicted structural parameters, and vibrational frequencies and those obtained experimentally. In order to understand halogen effect, 3-halogenobenzaldehyde [XC6H4CHO; X=F, Cl and Br] was also studied theoretically. The free energy difference between the isomers is small but the rotational barrier is about 8kcal/mol. An atypical behavior of fluorine affecting conformational preference is observed.

References

Jan 4, 2003·Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy·P Venkata Ramana Rao, G Ramana Rao
Jun 20, 2013·Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy·Michał H Jamróz
Jul 5, 2013·Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy·Mahir TursunMustafa Senyel

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