Titre :	Synthèse et caractérisation d’une nouvelle catégorie d’acide α-aminophosphonique à base d’imine : Evaluation expérimentale et théorique de leurs activités antioxydantes
Type de document :	document électronique
Auteurs :	Siham Kitouni, Auteur ; Nadjib Chafai, Directeur de thèse
Année de publication :	2024
Importance :	1 vol (139 f.)
Format :	29 cm
Langues :	Français (fre)
Catégories :	Thèses & Mémoires:Chimie
Mots-clés :	Base de Schiff  acide α-aminophosphonique  activité antioxydante  enthalpie de dissociation de liaison  affinité protonique  potentiel d'ionisation.
Index. décimale :	204- chimie
Résumé :	A Schiff base (I1) and its corresponding α-aminophosphonic acid (P1) were synthesized using a simple and rapid preparation method and with a chemical yield of up to 75 % and 68%, respectively. The structures of I1 and P1 were experimentally characterized by IR, 1H NMR, 13C NMR and 31P NMR spectroscopic methods. A test of their antioxidant activities was carried out and indicated that I1 and P1 were able to scavenge radicals. The main objective of this research was the theoretical study of the antioxidant power of I1 and P1. Density functional theory (DFT) calculations at the B3LYP/6-311+G(d, p) level were performed to determine BDE, PA, ETE, IP, PDE, spin density distribution parameters and HOMO-LUMO energies in order to study the antioxidant potential of the title products in the gas phase. According to the theoretical results, the abstraction of H atoms from the 2-OH and 1-OH groups of I1 and P1 compounds, respectively, is most preferable during the free radical scavenging process. In addition, it was shown that HAT is the thermodynamically dominant mechanism compared to SPLET and SET-PT. The calculated data of the antioxidant activity of I1 and P1 are consistent with the experimental results. A study of the chemical reactivity of these molecules was carried out. Calculations of the global parameters (chemical potential (μ), hardness (η), softness (S) and electrophilicity index (ω)) and Fukui indices of the studied compounds were done and discussed. These molecules have an electrophilic character. The Fukui functions were calculated to specify the interaction sites of these products.
Côte titre :	Dch/0037
En ligne :	http://dspace.univ-setif.dz:8888/jspui/handle/123456789/4401

Synthèse et caractérisation d’une nouvelle catégorie d’acide α-aminophosphonique à base d’imine : Evaluation expérimentale et théorique de leurs activités antioxydantes [document électronique] / Siham Kitouni, Auteur ; Nadjib Chafai, Directeur de thèse . - 2024 . - 1 vol (139 f.) ; 29 cm.
Langues : Français (fre)

Catégories :	Thèses & Mémoires:Chimie
Mots-clés :	Base de Schiff  acide α-aminophosphonique  activité antioxydante  enthalpie de dissociation de liaison  affinité protonique  potentiel d'ionisation.
Index. décimale :	204- chimie
Résumé :	A Schiff base (I1) and its corresponding α-aminophosphonic acid (P1) were synthesized using a simple and rapid preparation method and with a chemical yield of up to 75 % and 68%, respectively. The structures of I1 and P1 were experimentally characterized by IR, 1H NMR, 13C NMR and 31P NMR spectroscopic methods. A test of their antioxidant activities was carried out and indicated that I1 and P1 were able to scavenge radicals. The main objective of this research was the theoretical study of the antioxidant power of I1 and P1. Density functional theory (DFT) calculations at the B3LYP/6-311+G(d, p) level were performed to determine BDE, PA, ETE, IP, PDE, spin density distribution parameters and HOMO-LUMO energies in order to study the antioxidant potential of the title products in the gas phase. According to the theoretical results, the abstraction of H atoms from the 2-OH and 1-OH groups of I1 and P1 compounds, respectively, is most preferable during the free radical scavenging process. In addition, it was shown that HAT is the thermodynamically dominant mechanism compared to SPLET and SET-PT. The calculated data of the antioxidant activity of I1 and P1 are consistent with the experimental results. A study of the chemical reactivity of these molecules was carried out. Calculations of the global parameters (chemical potential (μ), hardness (η), softness (S) and electrophilicity index (ω)) and Fukui indices of the studied compounds were done and discussed. These molecules have an electrophilic character. The Fukui functions were calculated to specify the interaction sites of these products.
Côte titre :	Dch/0037
En ligne :	http://dspace.univ-setif.dz:8888/jspui/handle/123456789/4401