Synthesis, Structural Elucidation and Anion Binding Studies of Isophthalamide Derivatives as Potential Receptor for Chromate Anions
| Autor: | Ramizah Ramli, Syahirah Omar, Maisara Abdul Kadir, Nur Shuhaila Haryani Abd Haris |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
Multidisciplinary
Chromate conversion coating 05 social sciences Carbon-13 NMR Mass spectrometry Chloride Medicinal chemistry chemistry.chemical_compound chemistry Amide 0502 economics and business medicine Proton NMR 050211 marketing Fourier transform infrared spectroscopy Anion binding 050203 business & management medicine.drug |
| Zdroj: | Sains Malaysiana. 48:1473-1481 |
| ISSN: | 0126-6039 |
| DOI: | 10.17576/jsm-2019-4807-16 |
| Popis: | This study highlights the synthesis and structural elucidation of two new isophthalamide isomers namely N,N’-1,3-bis(4-methylpyridin-2-yl)isophthalamide (4-MPI) and N,N’-1,3-bis(5-methylpyridin-2-yl)isophthalamide (5-MPI), prepared from reaction between isophthaloyl chloride with 2-amino-4-methylpyridine and 2-amino-5-methylpyridine, respectively. Their potential studies as anion receptors for chromate anions are also include in this paper. Characterization of these compounds were accomplished using common spectroscopic techniques such as Fourier Transform Infrared (FT-IR), 1H and 13C Nuclear Magnetic Resonance (NMR), UV-Vis spectrometer and mass spectrometry. FTIR analysis showed the presence of four significant peaks comprising ν(N-H), ν(C-H), ν(C=O) and δ(N-H) at range 3256-3274 cm-1, 2812-2928 cm-1, 1662-1686 cm-1 and 1533-1537 cm-1, respectively. Meanwhile, 1H NMR confirmed the presence of methyl, aromatic carbon and amide resonances at δH 2.983-2.994 ppm, 6.860-8.974 and 10.138-11.300 ppm, respectively. In the 13C NMR spectra, the appearance of methyl, aromatic and carbonyl carbon signals were determined at δC 18.45-20.59 ppm, 108.42-159.22 ppm and 167.04-167.20 ppm, respectively. UV-Vis study showed that 4-MPI and 5-MPI shows promising potential as anion receptors for chromate anions. |
| Databáze: | OpenAIRE |
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