Synthesis, spectroscopy, semiempirical, phytotoxicity, antibacterial, antifungal, and cytotoxicity of diorganotin(IV) complex derived from Bu2Sn(Acac)2 and 4-methyl-1-piperidinecarbodithioic acid
作者:H. N. Khan、S. Ali、S. Shahzadi、S. K. Sharma、K. Qanungo
DOI:10.1134/s1070328410040123
日期:2010.4
New diorganotin(IV) derivative of 4-methyl-1-piperidinecarbodithioic acid (4-MePCDTA) have been synthesized by the reaction of dibutyltin(Acac)(2) and ligand acid in a 1: 1 molar ratio in anhydrous chloroform at room temperature. The newly synthesized complex has been characterized by elemental, IR, and multinuclear NMR (H-1 and C-13). The diorganotin(IV) derivative is assessed to adopt distorted octahedral geometry in the solid state, while tetrahedral geometry is exhibited in a solution state. The modeled structure of the reported complex shows severely distorted octahedral geometry around tin. The axial tin carbon bond lengths are 2.15 . The Sn-O bond lengths for coordinated Acac in the equatorial plane are 2.37 and 2.23 , respectively. The complex was also tested for antimicrobial activity against different bacterial and fungal strains, artemia salina cytotoxicity, and plant phytotoxicity. The screening results show that the complex exhibits high antibacterial, antifungal, and artemia salina cytotoxicity and have a potential to be used as drug. Low phytotoxic activity shows that the reported compound can be used as agrochemical. The structure-activity relationship demonstrates that the compound having four-coordinated geometry in the solution state is more toxic.