Theoretical study on adiabatic electron affinity of fatty acids. (25th August 2021)
- Record Type:
- Journal Article
- Title:
- Theoretical study on adiabatic electron affinity of fatty acids. (25th August 2021)
- Main Title:
- Theoretical study on adiabatic electron affinity of fatty acids
- Authors:
- Yang, Yaxin
Zheng, Wenrui
Xie, Hongyun
Ren, Lufei
Xu, Xiaofei
Liang, Yingning - Abstract:
- Abstract : The AEA of saturated fatty acids, monounsaturated fatty acids, and polyunsaturated fatty acids with typical substituents were calculated by the ωB97X method. Abstract : As nutrients, secondary metabolites, essential signal molecules and energy sources, fatty acids play a vital role in biomedicine, pharmacokinetics and human metabolism. The reduction of fatty acids is one of the main ways to control the synthesis of fatty aldehydes and fatty alcohols. The resulting fatty aldehydes and fatty alcohols play a key role in many fields. Therefore, the fatty acid reduction reaction is an important type of chemical reaction, and one of the thermodynamic properties of adiabatic electron affinity (AEA), which describes the ability of fatty acids to obtain electrons, has become particularly important. In our research, we first calculated the AEA of 26 carboxylic acid compounds by using theoretical methods including 5 composite ab initio methods (G3, G4, G3B3, CBS-QB3 and CBS-Q) and 34 density functional theory (DFT) methods. It is found that ωB97X provides the most accurate result with a minimum root mean square error (RMSE) of 1.35 kcal mol −1 . Therefore, the ωB97X method was used to study saturated and unsaturated fatty acids with different kinds of substituents. The results show that electron withdrawing groups (EWGs), electron donating groups (EDGs) and conjugated groups (CEG) have great and different effects on the AEA. In addition, natural bond orbital (NBO) analysisAbstract : The AEA of saturated fatty acids, monounsaturated fatty acids, and polyunsaturated fatty acids with typical substituents were calculated by the ωB97X method. Abstract : As nutrients, secondary metabolites, essential signal molecules and energy sources, fatty acids play a vital role in biomedicine, pharmacokinetics and human metabolism. The reduction of fatty acids is one of the main ways to control the synthesis of fatty aldehydes and fatty alcohols. The resulting fatty aldehydes and fatty alcohols play a key role in many fields. Therefore, the fatty acid reduction reaction is an important type of chemical reaction, and one of the thermodynamic properties of adiabatic electron affinity (AEA), which describes the ability of fatty acids to obtain electrons, has become particularly important. In our research, we first calculated the AEA of 26 carboxylic acid compounds by using theoretical methods including 5 composite ab initio methods (G3, G4, G3B3, CBS-QB3 and CBS-Q) and 34 density functional theory (DFT) methods. It is found that ωB97X provides the most accurate result with a minimum root mean square error (RMSE) of 1.35 kcal mol −1 . Therefore, the ωB97X method was used to study saturated and unsaturated fatty acids with different kinds of substituents. The results show that electron withdrawing groups (EWGs), electron donating groups (EDGs) and conjugated groups (CEG) have great and different effects on the AEA. In addition, natural bond orbital (NBO) analysis and geometric structural analysis and frontier orbital energy analysis was investigated to further reveal the change pattern of AEA values of fatty acids. … (more)
- Is Part Of:
- New journal of chemistry. Volume 45:Number 36(2021)
- Journal:
- New journal of chemistry
- Issue:
- Volume 45:Number 36(2021)
- Issue Display:
- Volume 45, Issue 36 (2021)
- Year:
- 2021
- Volume:
- 45
- Issue:
- 36
- Issue Sort Value:
- 2021-0045-0036-0000
- Page Start:
- 16892
- Page End:
- 16905
- Publication Date:
- 2021-08-25
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d1nj02456f ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 19621.xml