Orbital - Vol. 9 No. 1 - January - March 2017
FULL PAPERS

Synthesis, Evaluation of Substituent Effect and Antimicrobial Activities of Substituted (E)-1-(3-bromo-4-morpholinophenyl)-3-phenylprop-2-en-1-one Compounds

Selvaraj Balaji
PG & Research Department of Chemistry, Government Arts College
Murugan Rajarajan
PG & Research Department of Chemistry, Government Arts College
Renganathan Vijayakumar
PG & Research Department of Chemistry, Government Arts College
Venkatesan Manikandan
PG & Research Department of Chemistry, Government Arts College
Rajamohan Senbagam
PG & Research Department of Chemistry, Government Arts College
Ganesan Vanangamudi
PG & Research Department of Chemistry, Government Arts College
Ganesamoorthy Thirunarayanan
Department of Chemistry, Annamalai University, Annamalainagar
Published February 13, 2017
Keywords
  • synthesis,
  • UV,
  • IR,
  • NMR,
  • spectral correlation analysis,
  • substituent effects,
  • antimicrobial activities
  • ...More
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How to Cite
(1)
Balaji, S.; Rajarajan, M.; Vijayakumar, R.; Manikandan, V.; Senbagam, R.; Vanangamudi, G.; Thirunarayanan, G. Synthesis, Evaluation of Substituent Effect and Antimicrobial Activities of Substituted (E)-1-(3-Bromo-4-Morpholinophenyl)-3-Phenylprop-2-En-1-One Compounds. Orbital: Electron. J. Chem. 2017, 9, 1-17.

Abstract

A series of ten substituted (E)-1-(3-bromo-4-morpholinophenyl)-3-phenylprop-2-en-1-one compounds were synthesized by Crossed-Aldol condensation of 3-bromo-4-marpholino acetophenone with various substituted and unsubstituted benzaldehydes in presence of sodium hydroxide. The entire ten compounds are novel and these have been newly synthesized compounds. The synthesized substituted 3-phenylprop-2-en-1-one were characterized by their physical constants and UV, IR, NMR spectral data. These observed UV absorption maximum (λmax nm) value. The group frequencies of infrared absorption (cm-1) of νCO s-cis and s-trans, deformation modes of νCH out of plane and in-plane, νCH=CH out of plane, ν>C=C<out of plane values, 1H chemical shifts (ppm) vinyl protons, 13C chemical shifts (ppm) carbonyl carbons and vinyl carbons values were correlated with various Hammett substituent constants, and Swain-Lupton parameters using single and multi-regression analyses. From the results of statistical analysis, the effects of substituents on the functional group frequencies were studied. The antimicrobial activities of these synthesized substituted (E)-1-(3-bromo-4-morpholinophenyl)-3-phenylprop-2-en-1-ones have been screened using Kirby-Bauer method.

DOI: http://dx.doi.org/10.17807/orbital.v9i1.852