Studying the geometric parameters, stability of isomer and IR frequencies in Enaminone compounds with the DFT and HF methods: A theoretical study

Authors

  • Majid Saghi Department of chemistry, Arak Branch, Islamic Azad University, Arak, Iran
  • Ali Lotfi Department of chemistry, Quchan Branch, Islamic Azad University,Quchan, Iran
  • Mohammad Hosein Bigtan Department of chemistry, Arak Branch, Islamic Azad University, Arak, Iran
  • Reza Zare Department of chemistry, Quchan Branch, Islamic Azad University,Quchan, Iran

Keywords:

Enaminone; Isomer; Geometric parameters; HF; DFT

Abstract

Enaminones are the large category of chemical compounds that their numerous applications caused to be interested by researchers and scientists in two important experimental and theoretical forms. Calculating chemistry as one of the vital field for the chemistry can help us to investigate of enaminone structures. Our three isomers of the compounds are enaminone. In this research, Sustainability and inter-molecular hydrogen bond strength of each isomer is investigated. Four methods HF, B3LYP, B3P86, B3PW91 and two basis set 6-311G**, 6-311++G** were used in order to making calculation. The results of calculations in geometry parameters indicated that in our parameters, B3P86 method and 6-311++G** basis set have considerable preference than other methods and basis sets. In regarding to this method and basis set, hydrogen bonding was investigated and the third isomer (III) showed the strongest hydrogen bond achieved. Finally theoretical vibrational frequencies, in B3P86/6-311++G** basis set was investigated.

References

Elias, R.S., 2010. Theoretical study of the proton transfer in enaminones. Am. J. Applied Sci., 9, 103-106.

Michael, J.P., De Koning, C.B., Gravestock, D., Hosken, G.D., Howard A.S., Christa, M., Jungmann, C.M., Krause, R.W.M., Parsons, A.S., Pllley, S.C., Stanbury, T.V., 1999. Enaminones: versatile intermediates for natural product synthesis. Pure Applied Chem., 71, 979-988.

Almazroa, S., Elnagdi, M.H., El-Din, A.M.S., 2004. Studies with enaminones: The reaction of enaminones with amino heterocycles. A route to azolopyrimidines, azolopyridines and quinolones. J. Heterocyclic Chem., 41, 267-272.

Ruffino, B., Zanetti, M., 2009. Adsorption Study of Several Hydrophobic Organic Contaminants on an Aquifer Material. Am. J. Environ. Sci., 5, 508-516.

Shawali, A.S., 2010. Synthesis, reactions and antitumour screening of new enaminones. J. Chem. Res., 34, 630-634.

Junior, A.W., Oliveira, A.R.M., de Chunha, C.J., Simonelli, F., Marques, F.A., 1999. Synthesis of enaminones with stationary stereochemistry. J. Braz. Chem. Soc., 10, 369-374.

Elassar, A.Z.A., Elkhair, A.A., 2003. Recent developments in the chemistry of enaminones. Tetrahedron., 59, 8463-8480.

Reidlinger, C., Dworczak, R., Junk, H., 1998. Cyanoacetophenone as a Synthon for 1,4,5-Substituted pyrazoles. Monatshefte für Chemie/Chemical Monthly., 129, 1207-1211.

Cocco, M.T., Congiu, C., Onnis, V., Bernard, A.M., Piras, P.P., 1997. Synthesis of new fluorinated 1,5-benzoxazepine derivatives. J. Heterocycl. Chem., 34, 1347-1350.

Wiberg, K.B., Snoonian, J.R., 1998. Ring Expansion and Contraction of a Two-Carbon Bridged Spiropentane. J. Org. Chem., 63, 1390-1401.

Katritzky, A.R., Fang, Y., Donkor, A., Xu, J., 2000. Imine Acylation via Benzotriazole Derivatives: The Preparation of Enaminones. J. Synthesis., 14, 2029-2032.

Mahmud, T., Rehman, R., Gulzar, A., Khalid, A., Anwar, J., Shafique, U., uz. Zaman, W., Salman, M., 2010. Synthesis, characterization and study of antibacterial activity of enaminone complexes of zinc and iron. Arabian Journal of chemistry., 3, 219-224.

Edafiogho, I.O., Phillips, O.A., Udo, E.E., Samuel, S., Rethish, B., 2009. Synthesis, antibacterial and anticonvulsant evaluations of some cyclic enaminones. Eur. J. Med. Chem., 44, 967-975.

Purnami, S.W., Embong, A., Zain, J.M., Rahayu, S.P., 2009. A New Smooth Support Vector Machine and Its Applications in Diabetes Disease Diagnosis. J. Comput. Sci., 5, 1003-1008.

Moradi, S., Rajabi Mehr F., Baharvand, A., Rostami, C., 2008. Synthesis of Enaminones and Their Reaction with Dimethyl Acetylene Dicarboxylate. Iran. J. Chem. Chem. Eng., 27, 17-23.

Antonov, L., 2013. Tautomerism: Methods and Theories (1st ed.). Weinheim: Wiley-VCH.

Smith, M.B., March, J., 2001. Advanced Organic Chemistry (5th ed.). New York: Wiley Interscience. pp. 1218–1223.

Katritzky, A.R., Elguero, J., et al., 1976. The Tautomerism of heterocycles. New York: Academic Press.

Petrucci, R.H., Harwood, R.S., Herring, F.G., 2002. General Chemistry (8th ed). Prentice-Hall.

Berzelius, J.J., 1830. The word "isomer" was coined by Swedish chemist. 1779–1848.

Published

2015-05-29

How to Cite

Saghi, M. ., Lotfi, A. ., Hosein Bigtan, M. ., & Zare, R. . (2015). Studying the geometric parameters, stability of isomer and IR frequencies in Enaminone compounds with the DFT and HF methods: A theoretical study. Scientific Journal of Review, 4(5), 71-77. Retrieved from http://sjournals.com/index.php/sjr/article/view/439

Issue

Section

Chemistry