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Electrochemical Reduction Potential Correlation of some Insect Antifeedant Potent 2-Phenothiazinyl Chalcones

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Abstract:

A series containing twelve substituted styryl 2-phenothiazenyl ketones have been synthesized. The electrochemical potentials of carbonyl and vinyl groups were measured. These potentials are correlated with Hammett substituent constants, F and R parameters. From the results of statistical analyses, the effects of substituent on the group reduction potentials have been discussed. The insect antifeedant activities of these chalcones have been studied using 4th instar larvae Achoea Janata L with castor leaf discs.

Info:

Periodical:
International Letters of Chemistry, Physics and Astronomy (Volume 4)
Pages:
66-75
Citation:
K. Ranganathan et al., "Electrochemical Reduction Potential Correlation of some Insect Antifeedant Potent 2-Phenothiazinyl Chalcones", International Letters of Chemistry, Physics and Astronomy, Vol. 4, pp. 66-75, 2012
Online since:
November 2012
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Cited By:

[1] K. Sathiyamoorthi, V. Mala, S. Sakthinathan, D. Kamalakkannan, R. Suresh, G. Vanangamudi, G. Thirunarayanan, "Solvent-free synthesis, spectral correlations and antimicrobial activities of some aryl E 2-propen-1-ones", Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, Vol. 112, p. 245, 2013

DOI: https://doi.org/10.1016/j.saa.2013.04.048

[2] N. Nohut Maşlakcı, A. Biçer, G. Turgut Cin, A. Uygun Öksüz, "Electrochromic properties of some bis-chalcone derivatives-based nanofibers", Journal of Applied Polymer Science, Vol. 135, p. 46010, 2018

DOI: https://doi.org/10.1002/app.46010

[3] H. Gul, C. Yamali, G. Gunesacar, H. Sakagami, N. Okudaira, Y. Uesawa, H. Kagaya, "Cytotoxicity, apoptosis, and QSAR studies of phenothiazine derived methoxylated chalcones as anticancer drug candidates", Medicinal Chemistry Research, 2018

DOI: https://doi.org/10.1007/s00044-018-2242-5