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实验红外光谱、拉曼光谱和紫外可见光谱:密度泛函理论结构与构象研究——甲基丁香酚的生物活性及溶剂对其分子性质的影响

Experimental IR, Raman, and UV-Vis Spectra DFT Structural and Conformational Studies: Bioactivity and Solvent Effect on Molecular Properties of Methyl-Eugenol.

作者信息

Yadav Rohit Kumar, Yadav Bhoopendra, Yadav R A, Kostova Irena

机构信息

Department of Physics, Institute of Science, Banaras Hindu University, Varanasi 221005, India.

Department of Chemistry, Faculty of Pharmacy, Medical University, 2 Dunav St., 1000 Sofia, Bulgaria.

出版信息

Molecules. 2023 Jul 14;28(14):5409. doi: 10.3390/molecules28145409.

Abstract

Structural, conformational, and spectroscopic investigations of methyl-eugenol were made theoretically at the IR, Raman, and UV-vis spectra were investigated and analyzed in light of the computed quantities. Conformational analysis was carried out with the help of total energy vs. dihedral angle curves for different tops, yielding 21 stable conformers, out of which only two have energies below the room temperature relative to the lowest energy conformer. The effect of the solvent on different molecular characteristics was investigated theoretically. MEP and HOMO-LUMO analysis were carried out and barrier heights and bioactivity scores were determined. The present investigation suggests that the molecule has three active sites with moderate bioactivity. The solvent-solute interaction is found to be dominant in the vicinity of the methoxy moieties.

摘要

对甲基丁香酚进行了结构、构象和光谱学理论研究,并根据计算结果对红外、拉曼和紫外可见光谱进行了研究与分析。借助不同构象体的总能量与二面角曲线进行构象分析,得到21个稳定构象体,其中只有两个相对于最低能量构象体的能量在室温以下。从理论上研究了溶剂对不同分子特性的影响。进行了分子静电势(MEP)和最高占据分子轨道-最低未占据分子轨道(HOMO-LUMO)分析,并确定了势垒高度和生物活性分数。本研究表明该分子有三个具有中等生物活性的活性位点。发现溶剂-溶质相互作用在甲氧基部分附近占主导地位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844f/10386374/8358e41303a1/molecules-28-05409-g001.jpg

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