两种吖啶酮生物碱的结构、电子和 NLO 特性:DFT 和 TD-DFT 研究。

IF 2.1 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Vincent de Paul Zoua, Albert Fouda Atangana, Atud Quiggle Asi, Ismaèl Figapka Pagoré, Simplice Joel Ndendoung Tatsimo, Rahman Abdoul Ntieche
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引用次数: 0

摘要

背景:本研究从理论上考察了 Verdoocridone A(Ver A)和 B(Ver B)的结构、电子和非线性光学特性。结果表明,Ver A 和 B 具有良好的电子特性,可作为新材料应用于非线性光学领域。根据它们的最大吸收波长,Ver A(λmax = 313 nm)可以生成维生素 D,而 Ver B(λmax = 319.55 nm)则有助于皮肤色素沉着:所有计算均使用高斯 16 软件包在 DFT/B3LYP-D3/6-311 + G(d,p) 理论水平上进行。激发态是在 CAM-B3LYP 结合 6-311 + (d,p) 基集上使用 TD-DFT 方法模拟的。此外,还利用基于密度的溶解模型(SMD)方法研究了水相和苯相中的溶剂效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Structural, electronic, and NLO properties of two acridone alkaloîds: DFT and TD-DFT studies.

Structural, electronic, and NLO properties of two acridone alkaloîds: DFT and TD-DFT studies.

Context: The structural, electronic, and nonlinear optical properties of Verdoocridone A (Ver A) and B (Ver B) are examined theoretically in this study. The results showed that Ver A and B exhibit good electronic properties and can be used as new materials in NLO applications. According to their maximum absorption wavelength, Ver A (λmax = 313 nm) enables production of vitamin D, while Ver B (λmax = 319.55 nm) can help skin pigmentation.

Methods: All calculations were performed at the DFT/B3LYP-D3/6-311 + G(d,p) level of theory using the Gaussian 16 software package. Excited states were simulated using the TD-DFT method at the CAM-B3LYP combined with 6-311 + (d,p) basis set. Also, the solvent effect was studied in water and benzene phases by the solvation model based on density (SMD) method.

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来源期刊
Journal of Molecular Modeling
Journal of Molecular Modeling 化学-化学综合
CiteScore
3.50
自引率
4.50%
发文量
362
审稿时长
2.9 months
期刊介绍: The Journal of Molecular Modeling focuses on "hardcore" modeling, publishing high-quality research and reports. Founded in 1995 as a purely electronic journal, it has adapted its format to include a full-color print edition, and adjusted its aims and scope fit the fast-changing field of molecular modeling, with a particular focus on three-dimensional modeling. Today, the journal covers all aspects of molecular modeling including life science modeling; materials modeling; new methods; and computational chemistry. Topics include computer-aided molecular design; rational drug design, de novo ligand design, receptor modeling and docking; cheminformatics, data analysis, visualization and mining; computational medicinal chemistry; homology modeling; simulation of peptides, DNA and other biopolymers; quantitative structure-activity relationships (QSAR) and ADME-modeling; modeling of biological reaction mechanisms; and combined experimental and computational studies in which calculations play a major role.
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