330592-55-7Relevant academic research and scientific papers
Spectral characterization and antimicrobial activity of some schiff bases derived from 4-chloro-2-aminophenol and various salicylaldehyde derivatives
Cinarli, Adem,Guerbuez, Demet,Tavman, Aydin,Birteksoez, A. Seher
, p. 449 - 459 (2012)
A series of N-(5-chloro-2-hydroxyphenyl)-(3/4/5-substituted)- salicylaldimines (I-XI) were synthesized using appropriate synthetic route. Their structures were characterized by FT-IR, UV-Visible, ESI-MS, 1H and 13C NMR spectroscopic techniques and analytical methods. The crystal structure of N-(5-chloro-2-hydroxyphenyl)-5-bromosalicylaldimine (V) was determined by X-ray diffraction at room temperature. Relationship between the melting points and the structures of the compounds was examined. Antimicrobial activity of the compounds was evaluated against Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Proteus mirabilis. Antifungal activities were reported for Candida albicans. Schiff bases showed considerable antimicrobial activity against S. aureus, S. epidermidis and C. albicans. N-(5-Chloro-2-hydroxyphenyl)-3-hydroxy- salicylaldimine (II) has the broadest and highest antimicrobial activity according to the others. A series of N-(5-chloro-2-hydroxyphenyl)-(3/4/5- substituted)-salicylaldimines (I-XI) were synthesized using appropriate synthetic route. Relationship between the melting points and the structures of the compounds was examined. Antifungal activities were reported for Candida albicans. Schiff bases showed considerable antimicrobial activity against S. aureus, S. epidermidis and C. albicans. N-(5-Chloro-2-hydroxyphenyl)-3-hydroxy- salicylaldimine (II) has the broadest and highest antimicrobial activity. Copyright
Synthesis, crystal structure and biological activity of the Schiff base organotin(IV) complexes based on salicylaldehyde-o-aminophenol
Tan, Yu-Xing,Zhang, Zhi-Jian,Liu, Yang,Yu, Jiang-Xi,Zhu, Xiao-Ming,Kuang, Dai-Zhi,Jiang, Wu-Jiu
, p. 874 - 881 (2017)
Schiff base organotin(IV) complexes C1 ～ C5b have been synthesized via the reaction of the substituted salicylaldehyde-o-aminophenol Schiff base ligands (L1 ～ L3) with the dibenzyltin dichloride, n-butyltin trichloride or dibutyltin oxide, respectively. T
