Open AccessSynthesis, characterization and the antifungal activity test of some organotin(IV) benzoates
Author(s) -
Sutopo Hadi,
B. Irawan,
Yandri,
Tati Suhartati
Publication year - 2021
Publication title -
journal of physics. conference series
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 85
eISSN - 1742-6596
pISSN - 1742-6588
DOI - 10.1088/1742-6596/1751/1/012099
Subject(s) - chemistry , benzoates , benzoic acid , fusarium oxysporum , antifungal , nuclear chemistry , proton nmr , medicinal chemistry , stereochemistry , organic chemistry , medicine , botany , dermatology , biology
In continuing search on the biological activity of the organotin compounds we are working with, We here reported the synthesis and the antifungal activity test of three organotin(IV) complexes of dibutyltin(IV) dibenzoate ( 3 ), diphenyltin(IV) dibenzoate ( 6 ) and triphenyltin(IV) benzoate ( 9 ). These three compounds were prepared by the reaction of dibutyltin(IV) dichloride ( 1 ), diphenyltin(IV) dichloride ( 4 ), and triphenyltin(IV) chloride ( 7 ) via dibutyltin(IV) oxide ( 2 ), diphenyltin(IV) oxide ( 5 ), and triphenyltin(IV) hydroxide ( 8 ) with benzoic acid. The product obtained in each step was characterized by UV, IR and NMR spectroscopies and also microelemental analysis. The antifungal activity test was carried out against Fusarium oxysporum strain. The results showed that the inhibition zone shown by these organotin(IV) benzoate were found by far much more active compared to the free benzoic acid, the starting materials 1, 4, 7 , and the intermediate products, 2, 5 and 8 . The inhibition zone of each of the compounds tested was compared with the control where the fungus alone was grown in the media. The results showed that triphenyltin(IV) benzoate ( 9 ) was the most active compound against the fungus and the minimum inhibitory concentration obtained was about 0.7 mM.