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Journals / Journal of the Turkish Chemical Society Section A: Chemistry / 2026 / Volume: 6 Issue: 2

Synthesis, Molecular Structure, Hirshfeld Surface Analysis, Spectroscopic and Computational Studies (DFT) of 6,6'-((1E,1'E)- (1,2-phenylenebis(azanylylidene))bis(methanylylidene))bis(2- (tert-butyl)-4-methylphenol)

Pınar Şen(Rhodes University)0000-0002-3181-9890
Sevgi Kansız(ONDOKUZ MAYIS ÜNİVERSİTESİ)0000-0002-8433-7975
Necmi Dege(ONDOKUZ MAYIS ÜNİVERSİTESİ)0000-0003-0660-4721
Pages
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Publication Date
2019-06-15
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Hirshfeld surface analyses and two dimensional fingerprint plots were used to analyse the intermolecular interactions present in the crystal, indicating that the most important contributions for the crystal packing are from H ∙∙∙ H (71.2%), H ∙∙∙ C/C ∙∙∙ H (18.7%), C ∙∙∙ C (4.8%) and H ∙∙∙ N/N ∙∙∙ H (2.7%) interactions.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Schiff bases have been used in biological processes and as chelating agents for several decades.
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Key Findings & Data:This work presents the synthesis and characterization of compound, N,N’-Bis(3-tert-Butyl-5-methylsalicylidene)-1,2-diamino phenylene as the Schiff base derivative with the reaction of an aromatic aldehyde derivative and o-phenylenediamine.
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Conclusion & Impact:Hirshfeld surface analyses and two dimensional fingerprint plots were used to analyse the intermolecular interactions present in the crystal, indicating that the most important contributions for the crystal packing are from H ∙∙∙ H (71.2%), H ∙∙∙ C/C ∙∙∙ H (18.7%), C ∙∙∙ C (4.8%) and H ∙∙∙ N/N ∙∙∙ H (2.7%) interactions.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Synthesis · Crystal structure · Schiff base

Abstract

Schiff bases have been used in biological processes and as chelating agents for several decades. This work presents the synthesis and characterization of compound, N,N’-Bis(3-tert-Butyl-5-methylsalicylidene)-1,2-diamino phenylene as the Schiff base derivative with the reaction of an aromatic aldehyde derivative and o-phenylenediamine. The spectroscopic properties of the compound were examined by FT-IR, 1H NMR, 13C NMR, MS and elemental analyses. The molecular structure of the compound was also confirmed using X-ray single-crystal data. And also theoretical calculations were obtained by using Density Functional Theory (DFT) methods. The structural parameters were calculated by using DFT/B3LYP/6-31G(d,p) basis set in ground state. Molecular Electrostatic Potential (MEP) map and the frontier molecular orbitals (HOMO-LUMO) of the compound were created by using the optimized structures. The results of theoretical study using the DFT method at the B3LYP/6–31G(d,p) level are in good agreement with the experimental data. Hirshfeld surface analyses and two dimensional fingerprint plots were used to analyse the intermolecular interactions present in the crystal, indicating that the most important contributions for the crystal packing are from H ∙∙∙ H (71.2%), H ∙∙∙ C/C ∙∙∙ H (18.7%), C ∙∙∙ C (4.8%) and H ∙∙∙ N/N ∙∙∙ H (2.7%) interactions.

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Cite This Article

Şen, P., Kansız, S., Dege, N. (2019). Synthesis, Molecular Structure, Hirshfeld Surface Analysis, Spectroscopic and Computational Studies (DFT) of 6,6'-((1E,1'E)- (1,2-phenylenebis(azanylylidene))bis(methanylylidene))bis(2- (tert-butyl)-4-methylphenol). Journal of the Turkish Chemical Society Section A: Chemistry, Volume: 6 Issue: 2. https://doi.org/10.18596/jotcsa.483143

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