Huda E.M. Amin, O. Ali, Samir M. EL-Medania, A. S. Sayed
{"title":"新型Cr(III)、Co(II)、Ni(II)和Cu(II)席夫碱配合物的合成、光谱和抗菌性能","authors":"Huda E.M. Amin, O. Ali, Samir M. EL-Medania, A. S. Sayed","doi":"10.20431/2349-0403.0601004","DOIUrl":null,"url":null,"abstract":"Schiff bases are condensation products of primary amine and aliphatic or aromatic carbonyl compounds with the general formula (RCH=N-R), that makes the schiff base a stable imine. The linkage azomethine group contains a pair of π electrons bonded between carbon and nitrogen (CH=N-). In addition, the nitrogen atom present in the azomethine group has a lone pair of electron and this add distinct properties to this group. Schiff bases derived from aromatic amines and aromatic aldehydes have a wide variety of applications in many fields, eg., biological [1-4], Heterogenous catalyst [5], oxidation of alkanes [6], catalytic applications [7,8] and photo luminescent properties [9,10].","PeriodicalId":13721,"journal":{"name":"International Journal of Advanced Research in Chemical Science","volume":"5 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, Spectroscopic and Antimicrobial of New Cr(III), Co(II), Ni(II) and Cu(II) Schiff Base Complexes\",\"authors\":\"Huda E.M. Amin, O. Ali, Samir M. EL-Medania, A. S. Sayed\",\"doi\":\"10.20431/2349-0403.0601004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Schiff bases are condensation products of primary amine and aliphatic or aromatic carbonyl compounds with the general formula (RCH=N-R), that makes the schiff base a stable imine. The linkage azomethine group contains a pair of π electrons bonded between carbon and nitrogen (CH=N-). In addition, the nitrogen atom present in the azomethine group has a lone pair of electron and this add distinct properties to this group. Schiff bases derived from aromatic amines and aromatic aldehydes have a wide variety of applications in many fields, eg., biological [1-4], Heterogenous catalyst [5], oxidation of alkanes [6], catalytic applications [7,8] and photo luminescent properties [9,10].\",\"PeriodicalId\":13721,\"journal\":{\"name\":\"International Journal of Advanced Research in Chemical Science\",\"volume\":\"5 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Advanced Research in Chemical Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20431/2349-0403.0601004\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Advanced Research in Chemical Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20431/2349-0403.0601004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis, Spectroscopic and Antimicrobial of New Cr(III), Co(II), Ni(II) and Cu(II) Schiff Base Complexes
Schiff bases are condensation products of primary amine and aliphatic or aromatic carbonyl compounds with the general formula (RCH=N-R), that makes the schiff base a stable imine. The linkage azomethine group contains a pair of π electrons bonded between carbon and nitrogen (CH=N-). In addition, the nitrogen atom present in the azomethine group has a lone pair of electron and this add distinct properties to this group. Schiff bases derived from aromatic amines and aromatic aldehydes have a wide variety of applications in many fields, eg., biological [1-4], Heterogenous catalyst [5], oxidation of alkanes [6], catalytic applications [7,8] and photo luminescent properties [9,10].