Les Inscriptions à la Bibliothèque sont ouvertes en
ligne via le site: https://biblio.enp.edu.dz
Les Réinscriptions se font à :
• La Bibliothèque Annexe pour les étudiants en
2ème Année CPST
• La Bibliothèque Centrale pour les étudiants en Spécialités
A partir de cette page vous pouvez :
Retourner au premier écran avec les recherches... |
Détail de l'indexation
D000690
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Ouvrages de la bibliothèque en indexation D000690
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Titre : Fonctionnalisations des chlorures d'acides : Applications des complexes du nickel actifs en catalyse homogéne à l'électrosynthèses des cétones: procédé par action d'amines tertiaires Type de document : texte imprimé Auteurs : Belkacemi, Hayet, Auteur ; Perichon, J., Directeur de thèse Editeur : Université Paris VI Année de publication : 1990 Importance : 62 f. Présentation : ill. Format : 30 cm. Note générale : Thèse d’État : Électrochimie : Paris, Université Paris VI : 1990
Annexe f. 63 - 66 . Bibliogr. : 67 - 69 f.Langues : Français (fre) Mots-clés : Chlorures -- acides ; Nickel actifs ; Catalyse homogène ; Electrosynthèses des cétones ; Amines tertiaires ; Acétonitrile Index. décimale : D000690 Résumé : L'objectif principal, que nous nous sommes fixé pour l'ensemble des expériences menées au laboratoire, est surtout la réalisation d'un meilleur moyen technique et essentiellement électrochimique permettant la fonctionnalisation des chlorures d'acide.
En prenant comme point de départ celui qui consiste à réaliser des réactions de couplages mixtes entre les chlorures d'acide et les halogènures d'alkyls pour aboutir principalement aux formations de cétones symétriques et dissymétriques.
Le but essentiellement visé à l'origine de ce travail, était l'activation de liaisons carbone-halogène par des complexes du nickel.
Compte tenu des performances présentées par un nouveau procédé utilisant une anode soluble, il nous a semblé plus judicieux d'orienter nos recherches vers d'autres thèmes où, tout en profitant de l'avantage technique (absence de séparateur) de ce nouveau procédé, la catalyse par des complexes du nickel s'avérait nécessaire pour la sélectivité des réactions envisagées.Fonctionnalisations des chlorures d'acides : Applications des complexes du nickel actifs en catalyse homogéne à l'électrosynthèses des cétones: procédé par action d'amines tertiaires [texte imprimé] / Belkacemi, Hayet, Auteur ; Perichon, J., Directeur de thèse . - [S.l.] : Université Paris VI, 1990 . - 62 f. : ill. ; 30 cm.
Thèse d’État : Électrochimie : Paris, Université Paris VI : 1990
Annexe f. 63 - 66 . Bibliogr. : 67 - 69 f.
Langues : Français (fre)
Mots-clés : Chlorures -- acides ; Nickel actifs ; Catalyse homogène ; Electrosynthèses des cétones ; Amines tertiaires ; Acétonitrile Index. décimale : D000690 Résumé : L'objectif principal, que nous nous sommes fixé pour l'ensemble des expériences menées au laboratoire, est surtout la réalisation d'un meilleur moyen technique et essentiellement électrochimique permettant la fonctionnalisation des chlorures d'acide.
En prenant comme point de départ celui qui consiste à réaliser des réactions de couplages mixtes entre les chlorures d'acide et les halogènures d'alkyls pour aboutir principalement aux formations de cétones symétriques et dissymétriques.
Le but essentiellement visé à l'origine de ce travail, était l'activation de liaisons carbone-halogène par des complexes du nickel.
Compte tenu des performances présentées par un nouveau procédé utilisant une anode soluble, il nous a semblé plus judicieux d'orienter nos recherches vers d'autres thèmes où, tout en profitant de l'avantage technique (absence de séparateur) de ce nouveau procédé, la catalyse par des complexes du nickel s'avérait nécessaire pour la sélectivité des réactions envisagées.Exemplaires
Code-barres Cote Support Localisation Section Disponibilité Spécialité Etat_Exemplaire D000690 D000690 Papier Bibliothèque centrale Thèse de Doctorat Disponible Documents numériques
BELKACEMI.Hayet.pdfURL