Yi-Chen Chan, Abdussalam Salhin Mohamed Ali, M. Khairuddean, B. Salleh
{"title":"(E)-乙基-4-(2-氧苊-1(2H)-基氨基)苯甲酸酯的合成、晶体结构及抗菌活性","authors":"Yi-Chen Chan, Abdussalam Salhin Mohamed Ali, M. Khairuddean, B. Salleh","doi":"10.4236/JCPT.2013.32011","DOIUrl":null,"url":null,"abstract":"A Schiff base, (E)-ethyl-4-(2-oxoacenaphthylen-1(2H)-ylideneamino)benzoate, (E4AB) had been synthesized in good yield \nby the acid-catalyzed condensation reaction of acenaphthenequinone and \nethyl-4-aminobenzoate in methanolic solution. The synthesized compound was \nelucidated by elemental analysis (CHN), FTIR, 1H-NMR, 13C-NMR \nand single crystal X-ray diffraction. E4AB crystallized in the monoclinic \ncrystal system with space group P21/c, Z = 4, V = 1569.3(2) ?3 and unit \ncell parameters a = 9.1589(8) , b = 21.2003(17)?, c =8.4502(7) ?, β= 106.972(2)°. \nThe crystal structure of the compound is stabilized by intermolecular C-H···O hydrogen bonds and weak intermolecular π···π interactions. The title compound had been tested for \nthe antimicrobial activity against Bacillus \nsubtilis (B. subtilis), Enterobacter and Fusarium oxysporum f. sp. Cubense (Foc) by disc-diffusion method. \nE4AB is relatively active against Foc which is a pathogen that cause Wilt disease (also well known as Panama disease) \nin banana plantation.","PeriodicalId":64440,"journal":{"name":"结晶过程及技术期刊(英文)","volume":"38 1","pages":"69-73"},"PeriodicalIF":0.0000,"publicationDate":"2013-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Synthesis, Crystal Structure and Antimicrobial Activity of (E)-ethyl-4-(2-oxoacenaphthylen-1(2H)-ylideneamino) benzoate\",\"authors\":\"Yi-Chen Chan, Abdussalam Salhin Mohamed Ali, M. Khairuddean, B. Salleh\",\"doi\":\"10.4236/JCPT.2013.32011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A Schiff base, (E)-ethyl-4-(2-oxoacenaphthylen-1(2H)-ylideneamino)benzoate, (E4AB) had been synthesized in good yield \\nby the acid-catalyzed condensation reaction of acenaphthenequinone and \\nethyl-4-aminobenzoate in methanolic solution. The synthesized compound was \\nelucidated by elemental analysis (CHN), FTIR, 1H-NMR, 13C-NMR \\nand single crystal X-ray diffraction. E4AB crystallized in the monoclinic \\ncrystal system with space group P21/c, Z = 4, V = 1569.3(2) ?3 and unit \\ncell parameters a = 9.1589(8) , b = 21.2003(17)?, c =8.4502(7) ?, β= 106.972(2)°. \\nThe crystal structure of the compound is stabilized by intermolecular C-H···O hydrogen bonds and weak intermolecular π···π interactions. The title compound had been tested for \\nthe antimicrobial activity against Bacillus \\nsubtilis (B. subtilis), Enterobacter and Fusarium oxysporum f. sp. Cubense (Foc) by disc-diffusion method. \\nE4AB is relatively active against Foc which is a pathogen that cause Wilt disease (also well known as Panama disease) \\nin banana plantation.\",\"PeriodicalId\":64440,\"journal\":{\"name\":\"结晶过程及技术期刊(英文)\",\"volume\":\"38 1\",\"pages\":\"69-73\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-04-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"结晶过程及技术期刊(英文)\",\"FirstCategoryId\":\"1087\",\"ListUrlMain\":\"https://doi.org/10.4236/JCPT.2013.32011\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"结晶过程及技术期刊(英文)","FirstCategoryId":"1087","ListUrlMain":"https://doi.org/10.4236/JCPT.2013.32011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
在甲醇溶液中,苊醌与4-氨基苯甲酸乙酯酸催化缩合反应,合成了席夫碱(E)-乙基-4-(2-氧苊-1(2H)-酰基氨基苯甲酸乙酯(E4AB),收率较高。通过元素分析(CHN)、红外光谱(FTIR)、核磁共振(1H-NMR)、核磁共振(13C-NMR)和单晶x射线衍射对合成的化合物进行了表征。E4AB在单斜晶系中结晶,空间群为P21/c, Z = 4, V = 1569.3(2) ?3,晶胞参数a = 9.1589(8), b = 21.2003(17)?, c =8.4502(7)°,β= 106.972(2)°。分子间的C-H··O氢键和分子间的弱π··π相互作用稳定了化合物的晶体结构。采用圆盘扩散法测定了该化合物对枯草芽孢杆菌(Bacillus subtilis)、肠杆菌(Enterobacter)和镰刀菌(Fusarium oxysporum f. sp. Cubense)的抑菌活性。E4AB对引起香蕉种植园枯萎病(也称为巴拿马病)的病原菌Foc具有较强的抑制活性。
Synthesis, Crystal Structure and Antimicrobial Activity of (E)-ethyl-4-(2-oxoacenaphthylen-1(2H)-ylideneamino) benzoate
A Schiff base, (E)-ethyl-4-(2-oxoacenaphthylen-1(2H)-ylideneamino)benzoate, (E4AB) had been synthesized in good yield
by the acid-catalyzed condensation reaction of acenaphthenequinone and
ethyl-4-aminobenzoate in methanolic solution. The synthesized compound was
elucidated by elemental analysis (CHN), FTIR, 1H-NMR, 13C-NMR
and single crystal X-ray diffraction. E4AB crystallized in the monoclinic
crystal system with space group P21/c, Z = 4, V = 1569.3(2) ?3 and unit
cell parameters a = 9.1589(8) , b = 21.2003(17)?, c =8.4502(7) ?, β= 106.972(2)°.
The crystal structure of the compound is stabilized by intermolecular C-H···O hydrogen bonds and weak intermolecular π···π interactions. The title compound had been tested for
the antimicrobial activity against Bacillus
subtilis (B. subtilis), Enterobacter and Fusarium oxysporum f. sp. Cubense (Foc) by disc-diffusion method.
E4AB is relatively active against Foc which is a pathogen that cause Wilt disease (also well known as Panama disease)
in banana plantation.