Aouled, Idriss MahamoudUysal, Saban2024-09-292024-09-2920230022-28601872-8014https://doi.org/10.1016/j.molstruc.2023.135084https://hdl.handle.net/20.500.14619/5140In this study, tetraoxocalix[2]arene[2]triazine compound as starting compound codded as C1 was synthesized by reacting of 2,4,6-trichloro-1,3,5-triazine with methyl-3,5-dihydroxybenzoate in two stages. sTriazine bridged calixarene ligands as target ligands, which we coded as C2 and C3, were obtained from the reaction of C1 coded compound with 4-aminobenzoic acid or 4-hydroxybenzoic acid at 1:2 mole ratio, respectively. [MSalen/Saloph] capped benzoic acid substitute tetraoksocalix[2] aren[2]triazine complexes were obtained from the reaction of C2 or C3 codded ligand with [(MSalen/Saloph) 2 O] (M = Cr 3 + , Fe 3 + and Co 3 + ) starting complexes in 1,4-dioxane media. The ligands obtained were characterized by using 1 HNMR , FT-IR spectroscopy and elemental analysis techniques. The complexes obtained were characterized by using FT-IR, UV-vis spectroscopies, elemental analysis, magnetic susceptibility, and TGA-DTA techniques. Metal contents of the complexes were determined by using ICP-OES spectroscopy. (c) 2023 Elsevier B.V. All rights reserved.eninfo:eu-repo/semantics/closedAccesss-Triazine bridged calixarene complexesCalix[2]arene[2]triazinesSchiff BaseSalenSalophArticle10.1016/j.molstruc.2023.1350842-s2.0-85147541910Q21280WOS:000932623900001Q2