| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1327169 | Journal of Organometallic Chemistry | 2006 | 5 Pages |
Several new triphenyl- and tricyclohexyltin para-substituted benzoates were synthesized. Their structures were characterized by IR and Mössbauer spectroscopies. The structures were determined to be four-coordinated monomers. Larvicidal activities of the new compounds as well as other benzoates were evaluated against the 2nd larval instar of the Anopheles stephensi and Aedes aegypti mosquitoes. Results from the screening studies indicated that the triphenyltin benzoates were more toxic towards the Ae. aegypti larvae. A quantitative-structure activity relationship was also developed for the An. stephensi larvae.
Graphical abstractSeveral triphenyltin- and tricyclohexyltin para-substituted benzoates were synthesized and the larvicidal activities of the compounds were evaluated against the 2nd larval instar of the Anopheles stephensi and Aedes aegypti mosquitoes. Results from the screening studies indicated that the triphenyltin benzoates were more toxic towards the Ae. aegypti larvae. A quantitative structure activity relationship was also developed for the An. stephensi.Figure optionsDownload full-size imageDownload as PowerPoint slide
