通过DFT和NBO分析揭示的醇的CH异构体中的Schleyer类型的过度结合性芳香性
Pardis Naderi Dehkordi1, Hamid Saeidian2, Zohreh Mirjafary1
1Department of Chemistry, SR.C, Islamic Azad University, Tehran, Iran.
Scientific reports
|February 3, 2026
概括
替代品显著影响醇的芳香度. 基,基和基增强了它,而基则减少了它,为电子起源提供了新的见解.
科学领域:
- 有机化学 有机化学
- 计算化学的计算化学
背景情况:
- 芳香性是有机化学的一个基本概念.
- 传统的评估依赖于结构性,磁性和电子标准.
研究的目的:
- 通过使用DFT来研究替代剂对醇芳香度的影响.
- 使用多个指数和NBO分析量化芳香度.
主要方法:
- 密度函数理论 (DFT) 的计算.
- 对HOMED,BI,NICS(1) 和NICSzz(1) 指数的评估.
- 对电荷分布和稳定能量的自然键轨道 (NBO) 分析.
主要成果:
- 基,基和BH2替代剂增强了高结合性芳香性.
- 素,尤其是,降低了芳香度;CN组抑制了它.
- NH2和OH组显示温和的影响;在NICS指数和E之间发现了强烈的相关性.
结论:
- 替代物和定位异构体对醇中的过度结合性芳香度有着关键的影响.
- 这项研究为替代剂对芳香度的影响的电子起源提供了新的见解.
相关概念视频
Relation of DFT to z-Transform
825
The Discrete Fourier Transform (DFT) is a crucial tool for analyzing the frequency content of discrete-time signals. It converts a sequence of N samples from the time domain into its corresponding sequence in the frequency domain, where each sample represents a specific frequency component.
To understand how the DFT works, it's helpful to consider the z-transform, which is a method for representing discrete sequences in the complex frequency domain. The z-transform involves summing the...
To understand how the DFT works, it's helpful to consider the z-transform, which is a method for representing discrete sequences in the complex frequency domain. The z-transform involves summing the...
825
Constitutional Isomers of Alkanes
22.5K
Organic compounds of the same molecular formula can have different structural formulas called constitutional isomers, and the phenomenon is known as constitutional isomerism. Alkanes with four or more carbons showing multiple structures with the same molecular formula thereby exhibit constitutional isomerism.
The linear isomer of an alkane is prefixed by the term “n”; hence a linear isomer of pentane is known as n-pentane. Based on the type of branching, some of the...
The linear isomer of an alkane is prefixed by the term “n”; hence a linear isomer of pentane is known as n-pentane. Based on the type of branching, some of the...
22.5K
Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1
2.8K
Treating arylamines with nitrous acid gives aryldiazonium salts that are effective substrates in nucleophilic aromatic substitution reactions. The diazonio group in these salts can be easily displaced by different nucleophiles, yielding a wide variety of substituted benzenes. The leaving group departs as nitrogen gas, and this easy elimination is the driving force for the substitution reaction.
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...
2.8K
Classification of Titrimetric Analysis Based on Reaction Types
1.8K
Titrimetric analysis in solution chemistry involves measuring the volume of solutions and is often called volumetric analysis. The standard solution of known concentration in the burette is called the titrant, whereas the solution of unknown concentration in the flask is called the analyte, or titrand. Titrimetric analyses can be classified into four types based on the reactions between the titrant and analyte.
Titrations between an acid and a base lead to neutralization reactions that form...
Titrations between an acid and a base lead to neutralization reactions that form...
1.8K
Aromatic Compounds: Overview
14.0K
In general, the term ‘aromatic’ indicates a pleasant smell or fragrance from fresh flowers, freshly prepared coffee, etc. In the early history of organic chemistry, many benzene derivatives were isolated from the pleasant odor oils of the plants. For example, vanillin was isolated from the oil of vanilla, methyl salicylate from the oil of wintergreen, and cinnamaldehyde from the oil of cinnamon. They all had a pleasant odor; hence the name aromatic was given.
In 1825, Faraday isolated...
In 1825, Faraday isolated...
14.0K
Basicity of Aromatic Amines
8.1K
The basicity of aromatic amines is much weaker than that of aliphatic amines due to the involvement of the lone pair of electrons over the N atom in resonance with the aryl rings. Generally, the electron-donating ability of any substituents on the aryl ring of aromatic amines increases the basicity of the amine by increasing electron density, and hence the availability of lone pair on the nitrogen. On the other hand, electron-withdrawing functional groups on the aryl ring of amines decrease the...
8.1K


