Synthesis, characterization, and antioxidant activity of heterocyclic Schiff bases
Yazarlar (5)
Hakan Kızılkaya Batman University, Türkiye
Beşir Dağ Batman Üniversitesi, Türkiye
Tarık Aral Batman Üniversitesi, Türkiye
Doç. Dr. Nusret GENÇ Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Prof. Dr. Ramazan ERENLER Tokat Gaziosmanpaşa Üniversitesi, Türkiye
| Makale Türü |
Özgün Makale
(SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
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| Dergi Adı | Journal of the Chinese Chemical Society (Q3) | ||
| Dergi ISSN | 0009-4536 Dergi Bilgileri (2020) | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 09-2020 |
| Kabul Tarihi | 04-08-2020 | Yayınlanma Tarihi | 01-09-2020 |
| Cilt / Sayı / Sayfa | 67 / 9 / 1696–1701 | DOI | 10.1002/jccs.202000161 |
| Makale Linki | https://onlinelibrary.wiley.com/doi/abs/10.1002/jccs.202000161 | ||
| UAK Araştırma Alanları |
Organik Kimya
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| Özet |
| Schiff base derivatives have gained great importance due to revealing a great number of biological properties. Schiff bases were synthesized by treatment of 4‐amino‐1,5‐dimethyl‐2‐phenyl‐1H‐pyrazol‐3(2H)‐one (1) with various aldehydes in methanol at reflux. In addition, diamine was reacted with an aldehyde to yield the corresponding Schiff bases. The structures of synthesized Schiff bases were elucidated by spectroscopic methods such as microanalysis, 1H‐NMR, 13C‐NMR, and FTIR. Antioxidant activities of synthesized Schiff bases were carried out using different antioxidant assays such as 1,1‐diphenyl‐2‐picryl‐hydrazyl free radical (DPPH•) scavenging, 2,2′‐azino‐bis(3‐ethylbenzthiazoline‐6‐sulfonic acid) (ABTS) radical scavenging, and reducing power activity. (E)‐4‐((1H‐indol‐3‐yl)methyleneamino)‐1,5‐dimethyl‐2‐phenyl‐1H‐pyrazol‐3(2H)‐one (3), (E)‐1,5‐dimethyl‐4‐((2‐methyl‐1H‐indol‐3 … |
| Anahtar Kelimeler |
| antioxidant activity | chromatography | heterocyclic | Schiff base | spectroscopy | synthesis |
BM Sürdürülebilir Kalkınma Amaçları
| Atıf Sayıları | |
| Yöksis | 3 |
| Web of Science | 54 |
| Scopus | 58 |
| Google Scholar | 78 |