Synergistic integration of trifluoromethyl and phenolic moieties into novel hydrazone scaffolds: Synthesis, spectroscopic elucidation, and multidimensional antioxidant evaluation
Yazarlar (3)
Doç. Dr. Tolga Acar YEŞİL Sinop Üniversitesi, Türkiye
Öğr. Gör. Ömer Dilek Isparta Uygulamalı Bilimler Üniversitesi, Türkiye
Prof. Dr. Tahir Tilki Süleyman Demirel Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Journal of Molecular Structure (Q2)
Dergi ISSN 0022-2860 Dergi Bilgileri (2026)
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili Türkçe Basım Tarihi 01-2026
Kabul Tarihi Yayınlanma Tarihi 01-10-2026
Cilt / Sayı / Sayfa 1373 / 1 / – DOI 10.1016/j.molstruc.2026.146754
Makale Linki https://doi.org/10.1016/j.molstruc.2026.146754
UAK Araştırma Alanları
Organik Kimya Spektroskopi
Özet
Oxy-radical damage is a central mechanism in various diseases, prompting the search for novel scaffolds with enhanced stability and radical-scavenging efficiency. In this study, we report the design and synthesis of eight novel hydrazone derivatives (3a–h) featuring a synergistic integration of a metabolic-stabilizing trifluoromethyl (-CF 3 ) group and radical-scavenging phenolic hydroxyl moieties. The compounds were synthesized in high yields (80–92%), and FTIR, NMR, and mass spectrometry rigorously elucidated their structures. Crucially, comprehensive 2D COSY and NOESY NMR analyses in DMSO-d 6 using 3a as a representative model confirmed that the synthesized hydrazones exist exclusively in the thermodynamically favored, conformationally rigid E -configuration across the azomethine core. To decode the electronic environment, quantum chemical calculations were conducted using Density …
Anahtar Kelimeler
Antioxidant activity | Computational drug discovery | Phenolic compounds | Quantum chemical calculations | Trifluoromethylated hydrazones