{"title":"新型二-{2-乙氧基-6-[(3-取代-4,5-二氢- 1h -1,2,4-三唑-5- 1 -4基)亚甲基]苯基}对苯二甲酸酯的合成及酸强度的测定","authors":"Faruk Kardaş, H. Yüksek, Zafer Ocak","doi":"10.51435/turkjac.1109562","DOIUrl":null,"url":null,"abstract":"In this study, seven novel di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates (4a-g) were synthesized from the rections of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2a-g) with di-(2-formyl-6-ethoxyphenyl) terephtalate (3). The compounds 4a-g were characterized using by IR, 1H-NMR, 13C-NMR and UV spectral data. In addition, 4 type compounds were titrated potentiometrically with tetrabutylammonium hydroxide in four non-aqueous solvents such as isopropanol, tert-butanol, dimethyl ketone, N,N-dimethylformamide and the half-neutralization potential values and the corresponding pKa values were determined for all cases.","PeriodicalId":274781,"journal":{"name":"Turkish Journal of Analytical Chemistry","volume":"95 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and determination of acidity strength of some new di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates\",\"authors\":\"Faruk Kardaş, H. Yüksek, Zafer Ocak\",\"doi\":\"10.51435/turkjac.1109562\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, seven novel di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates (4a-g) were synthesized from the rections of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2a-g) with di-(2-formyl-6-ethoxyphenyl) terephtalate (3). The compounds 4a-g were characterized using by IR, 1H-NMR, 13C-NMR and UV spectral data. In addition, 4 type compounds were titrated potentiometrically with tetrabutylammonium hydroxide in four non-aqueous solvents such as isopropanol, tert-butanol, dimethyl ketone, N,N-dimethylformamide and the half-neutralization potential values and the corresponding pKa values were determined for all cases.\",\"PeriodicalId\":274781,\"journal\":{\"name\":\"Turkish Journal of Analytical Chemistry\",\"volume\":\"95 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Turkish Journal of Analytical Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.51435/turkjac.1109562\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Analytical Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51435/turkjac.1109562","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis and determination of acidity strength of some new di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates
In this study, seven novel di-{2-ethoxy-6-[(3-substitue-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)azomethine]phenyl} terephtalates (4a-g) were synthesized from the rections of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2a-g) with di-(2-formyl-6-ethoxyphenyl) terephtalate (3). The compounds 4a-g were characterized using by IR, 1H-NMR, 13C-NMR and UV spectral data. In addition, 4 type compounds were titrated potentiometrically with tetrabutylammonium hydroxide in four non-aqueous solvents such as isopropanol, tert-butanol, dimethyl ketone, N,N-dimethylformamide and the half-neutralization potential values and the corresponding pKa values were determined for all cases.