D. Kamalakkannan
Government Arts College, Coimbatore
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Featured researches published by D. Kamalakkannan.
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy | 2013
R. Suresh; D. Kamalakkannan; K. Ranganathan; R. Arulkumaran; R. Sundararajan; S.P. Sakthinathan; S. Vijayakumar; K. Sathiyamoorthi; V. Mala; Ganesan Vanangamudi; Kannan Thirumurthy; P. Mayavel; Ganesamoorthy Thirunarayanan
A series of aryl imines have been synthesized by Fly-ash: H2SO4 catalyzed microwave assisted process under solvent-free conditions. The yields of the imines have been found to be more than 87%. The purity of all imines has been checked using their physical constants and spectral data as published earlier in literature. The UV λmaxCN(nm), infrared νCN(cm(-1)), NMR δ(ppm) of CH and CN spectral data have been correlated with Hammett substituent constants and F and R parameters using single and multi-linear regression analysis. From the results of statistical analysis, the effect of substituents on the above spectral data has been studied. The antimicrobial activities of All synthesised imines have been studied using Bauer-Kirby method.
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy | 2013
K. Sathiyamoorthi; V. Mala; S.P. Sakthinathan; D. Kamalakkannan; R. Suresh; Ganesan Vanangamudi; Ganesamoorthy Thirunarayanan
Totally 38 aryl E 2-propen-1-ones including nine substituted styryl 4-iodophenyl ketones have been synthesised using solvent-free SiO2-H3PO4 catalyzed Aldol condensation between respective methyl ketones and substituted benzaldehydes under microwave irradiation. The yields of the ketones are more than 80%. The synthesised chalcones were characterized by their analytical, physical and spectroscopic data. The spectral frequencies of synthesised substituted styryl 4-iodophenyl ketones have been correlated with Hammett substituent constants, F and R parameters using single and multi-linear regression analysis. The antimicrobial activities of 4-iodophenyl chalcones have been studied using Bauer-Kirby method.
International Letters of Chemistry, Physics and Astronomy | 2013
S. Vijayakumar; R. Arulkumaran; R. Sundararajan; S.P. Sakthinathan; R. Suresh; D. Kamalakkannan; K. Ranganathan; K. Sathiyamoorthy; V. Mala; Ganesan Vanangamudi; Ganesamoorthy Thirunarayanan
International Letters of Chemistry, Physics and Astronomy | 2013
K. Ranganathan; R. Suresh; D. Kamalakkannan; R. Arulkumaran; R. Sundararajan; S.P. Sakthinathan; S. Vijayakumar; Ganesan Vanangamudi; Kannan Thirumurthy; P. Mayavel; Ganesamoorthy Thirunarayanan
Archive | 2012
D. Kamalakkannan; Ganesan Vanangamudi; R. Arulkumaran; Kannan Thirumurthy; P. Mayavel; Ganesamoorthy Thirunarayanan
International Letters of Chemistry, Physics and Astronomy | 2013
R. Arulkumaran; S. Vijayakumar; R. Sundararajan; S.P. Sakthinathan; D. Kamalakkannan; R. Suresh; K. Ranganathan; Ganesan Vanangamudi; Ganesamoorthy Thirunarayanan
QScience Connect | 2013
V. Mala; K. Sathiyamoorthi; Sp. Sakthinathan; D. Kamalakkannan; R. Suresh; Ganesan Vanangamudi; Ganesamoorthy Thirunarayanan
International Letters of Chemistry, Physics and Astronomy | 2014
N. Kalyanasundaram; S.P. Sakthinathan; R. Suresh; D. Kamalakkannan; S. John Joseph; Ganesan Vanangamudi; Ganesamoorthy Thirunarayanan
QScience Connect | 2013
R. Sundararajan; R. Arulkumaran; Srinivasan Vijayakumar; D. Kamalakkannan; R. Suresh; S. John Joseph; K. Ranganathan; Ganesan Vanangamudi; Muthuvel Subramanian; Ganesamoorthy Thirunarayanan; I. Muthuvel; B. Krishnakumar
International Letters of Chemistry, Physics and Astronomy | 2013
S.P. Sakthinathan; R. Suresh; V. Mala; K. Sathiyamoorthi; D. Kamalakkannan; K. Ranganathan; R. Arulkumaran; S. Vijayakumar; R. Sundararajan; Ganesan Vanangamudi; Ganesamoorthy Thirunarayanan