Synthesis, structural characterization by experimental and theoretical approaches of a new hydrazine derivative Schiff base compound

IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Molecular Crystals and Liquid Crystals Pub Date : 2023-08-17 DOI:10.1080/15421406.2023.2245648
Gonca Özdemir Tarı
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Abstract

AbstractIn this work, 6,6′-((1E,1′E)-hydrazine-1,2-diylidenebis(methanylylidene))bis(3,4-dimethoxyphenol), C18H20N2O6, which is a new symmetrical hydrazine derivative Schiff base compound was synthesized and characterized by elemental analysis, such as FT-IR and Raman, UV-Vis, NMR (1H and 13C) spectroscopies. In addition, the title compound’s thermal behavior was analyzed using TG/DTA techniques. The structure was determined by the X-ray diffraction (XRD) technique performed on a single crystal. Besides, computational methods were performed with the Density Functional Theory (DFT)/B3LYP method using the 6-311++G(d,p) basis set. The UV-Vis, chemical shifts for NMR, harmonic vibrational frequencies, infrared intensities, and Raman scattering activities in the ground state were performed same levels of theory. Intra- and inter-molecular interactions were determined using HS analysis. On the other hand, nucleophilic and electrophilic interactions were investigated using MEP and Fukui analysis. The experimental and computational results were compared comprehensively. To be able to examine the binding pattern of the compound with the PDB ID: 3BPF inhibitor targets were determined computationally by molecular docking studies. And also, HOMO and LUMO analysis, Mulliken and natural charge analysis, thermodynamic and non-linear optical properties were determined.Keywords: Density functional theoryHirshfeld surface analysishydrazine derivative Schiff basemolecular docking AcknowledgmentsI acknowledge to Scientific and Technological Research Application and Research Center, Sinop University, Turkey, for the use of the Bruker D8 QUEST diffractometer. I gratefully acknowledge the Eskisehir Osmangazi University, Central Research Laboratory Application and Research Center (ARUM) for the use of FT-IR and Raman spectroscopies, and the Mersin University, Advanced Technology Education Research and Application Center (MEITAM) for the use of NMR spectroscopy. I gratefully Dr. Seher Meral, Department of Chemistry, Faculty of Arts and Science, Ondokuz Mayıs University for her sincere help in the synthesis of the compound.
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一种新型联胺衍生物席夫碱化合物的合成、实验及理论表征
摘要本文合成了一种新的对称对称联胺衍生物希夫碱化合物6,6′-((1E, 1E)-肼-1,2-二乙基双(甲基乙基))-二(3,4-二甲氧基酚),C18H20N2O6,并用FT-IR、Raman、UV-Vis、NMR (1H和13C)等元素分析对其进行了表征。此外,采用TG/DTA技术分析了标题化合物的热行为。通过对单晶进行x射线衍射(XRD)技术测定了其结构。计算方法采用密度泛函理论(DFT)/B3LYP方法,采用6-311++G(d,p)基集。紫外可见性,核磁共振的化学位移,谐波振动频率,红外强度和拉曼散射活动在基态进行了相同的理论水平。分子内和分子间相互作用用HS分析测定。另一方面,利用MEP和Fukui分析研究了亲核和亲电相互作用。对实验结果和计算结果进行了综合比较。为了能够检测化合物与PDB的结合模式,我们通过分子对接研究计算确定了3BPF抑制剂的靶点。并进行了HOMO和LUMO分析、Mulliken和自然电荷分析、热力学和非线性光学性质的测定。关键词:密度泛函理论hirshfeld表面分析肼衍生物希夫碱分子对接感谢土耳其Sinop大学科技研究应用与研究中心使用Bruker D8 QUEST衍射仪。我感谢Eskisehir Osmangazi大学中央研究实验室应用和研究中心(ARUM)对FT-IR和拉曼光谱的使用,以及Mersin大学先进技术教育研究和应用中心(MEITAM)对核磁共振光谱的使用。我非常感谢Ondokuz Mayıs大学文理学院化学系Seher Meral博士在合成该化合物的过程中给予的真诚帮助。
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来源期刊
CiteScore
1.20
自引率
14.30%
发文量
248
审稿时长
2 months
期刊介绍: Established in 1966, Molecular Crystals and Liquid Crystals is a world-leading journal publishing original research papers in both an experimental and theoretical nature in three areas of specialization: liquid crystals, molecular crystals, and low-dimensional solids. These cover, but are not limited to: Liquid Crystals: -Electro- and magneto-optical phenomena; thermodynamics; phase transitions; structure; NMR and orientation-controlled spectroscopy; theory. Molecular Crystals: -Spectroscopy; energy and charge transfer; solid state reactions; photo and radiation effects Low-dimensional Solids: -Structure, electronic, magnetic, and optical properties; transport mechanisms The journal publishes research papers, review papers, and book reviews. In all three areas, experimental manuscripts describing both preparation and properties will be considered. Papers that describe determination of crystal structure alone are not encouraged unless some solid state forces (hydrogen bonding, charge transfer, etc.) are playing a significant role and/or some solid state properties of the materials are measured.
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