T. A. Ajayeoba, A.T. Famojuro, E. Akinkunmi, O. Olasehinde, A. O. Ayeni, O. Akinyele, J.A.O. Woods
{"title":"新型苄基丙酮-苯甲酰基腙及其对硝基和对羟基取代类似物的铜(ii)配合物的合成、表征和抗菌研究","authors":"T. A. Ajayeoba, A.T. Famojuro, E. Akinkunmi, O. Olasehinde, A. O. Ayeni, O. Akinyele, J.A.O. Woods","doi":"10.4314/ijs.v25i3.17","DOIUrl":null,"url":null,"abstract":"Three new ligands viz, benzylacetone-enzoylhydrazone [babh (L1)], para-hydroxy-benzylacetone-benzoylhydrazone [p-OH-babh (L2 )] and para-nitrobenzylacetone-benzoylhydrazone [p-NO2 -babh (L3 )], were synthesised by condensation of hydrazides with benzylacetone. The ligands were each reacted with copper(II) salts (chloride, nitrate, acetate and sulphate) to form complexes with the general formulae ML2X2 (X = Cl , NO3 , AcO- and SO4 ). The compounds were characterised using 1H NMR, Infrared and UV-Visible spectroscopy, as 4 well as CHN elemental analyser and magnetic susceptibility measurements. Antibacterial activity of the ligands and synthesised complexes were investigated using the agar diffusion method against two Gram-positive (Staphylococcus aureus NCTC 6571 and Bacillus cereus ATCC 11778) and three Gram- negative (Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 10145, Klebsiella pneumonia ATCC 13048) bacterial strains. However, the observed antimicrobial strength of the synthesized compounds was rather low.","PeriodicalId":13487,"journal":{"name":"Ife Journal of Science","volume":"67 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, characterisation and antibacterial study of copper(ii) complexes of new benzylacetone-benzoylhydrazone and its para-nitro and para-hydroxy substituted analogues\",\"authors\":\"T. A. Ajayeoba, A.T. Famojuro, E. Akinkunmi, O. Olasehinde, A. O. Ayeni, O. Akinyele, J.A.O. Woods\",\"doi\":\"10.4314/ijs.v25i3.17\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Three new ligands viz, benzylacetone-enzoylhydrazone [babh (L1)], para-hydroxy-benzylacetone-benzoylhydrazone [p-OH-babh (L2 )] and para-nitrobenzylacetone-benzoylhydrazone [p-NO2 -babh (L3 )], were synthesised by condensation of hydrazides with benzylacetone. The ligands were each reacted with copper(II) salts (chloride, nitrate, acetate and sulphate) to form complexes with the general formulae ML2X2 (X = Cl , NO3 , AcO- and SO4 ). The compounds were characterised using 1H NMR, Infrared and UV-Visible spectroscopy, as 4 well as CHN elemental analyser and magnetic susceptibility measurements. Antibacterial activity of the ligands and synthesised complexes were investigated using the agar diffusion method against two Gram-positive (Staphylococcus aureus NCTC 6571 and Bacillus cereus ATCC 11778) and three Gram- negative (Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 10145, Klebsiella pneumonia ATCC 13048) bacterial strains. However, the observed antimicrobial strength of the synthesized compounds was rather low.\",\"PeriodicalId\":13487,\"journal\":{\"name\":\"Ife Journal of Science\",\"volume\":\"67 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ife Journal of Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4314/ijs.v25i3.17\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ife Journal of Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4314/ijs.v25i3.17","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis, characterisation and antibacterial study of copper(ii) complexes of new benzylacetone-benzoylhydrazone and its para-nitro and para-hydroxy substituted analogues
Three new ligands viz, benzylacetone-enzoylhydrazone [babh (L1)], para-hydroxy-benzylacetone-benzoylhydrazone [p-OH-babh (L2 )] and para-nitrobenzylacetone-benzoylhydrazone [p-NO2 -babh (L3 )], were synthesised by condensation of hydrazides with benzylacetone. The ligands were each reacted with copper(II) salts (chloride, nitrate, acetate and sulphate) to form complexes with the general formulae ML2X2 (X = Cl , NO3 , AcO- and SO4 ). The compounds were characterised using 1H NMR, Infrared and UV-Visible spectroscopy, as 4 well as CHN elemental analyser and magnetic susceptibility measurements. Antibacterial activity of the ligands and synthesised complexes were investigated using the agar diffusion method against two Gram-positive (Staphylococcus aureus NCTC 6571 and Bacillus cereus ATCC 11778) and three Gram- negative (Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 10145, Klebsiella pneumonia ATCC 13048) bacterial strains. However, the observed antimicrobial strength of the synthesized compounds was rather low.