Mutual influence of gold and silver ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Mutual influence of gold and silver nanoparticles on Tris-(2,2 '''' bipyridine)-Ru (II) core complexes: Post-functionalization processes, optical and electrochemical investigations
Auteur(s) :
Dumur, F. [Auteur]
Institut de Chimie Radicalaire [ICR]
Guerlin, A. [Auteur]
Lehoux, A. [Auteur]
Institut Lavoisier de Versailles [ILV]
Selvakannan, P. R. [Auteur]
Miomandre, F. [Auteur]
Photophysique et Photochimie Supramoléculaires et Macromoléculaires [PPSM]
Meallet-Renault, R. [Auteur]
Institut des Sciences Moléculaires d'Orsay [ISMO]
Rebarz, M. [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Sliwa, Michel [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Dumas, E. [Auteur]
Le Pleux, L. [Auteur]
Chimie Et Interdisciplinarité : Synthèse, Analyse, Modélisation [CEISAM]
Pellegrin, Y. [Auteur]
Odobel, F. [Auteur]
Mayer, C. R. [Auteur]
Institut de Chimie Radicalaire [ICR]
Guerlin, A. [Auteur]
Lehoux, A. [Auteur]
Institut Lavoisier de Versailles [ILV]
Selvakannan, P. R. [Auteur]
Miomandre, F. [Auteur]
Photophysique et Photochimie Supramoléculaires et Macromoléculaires [PPSM]
Meallet-Renault, R. [Auteur]
Institut des Sciences Moléculaires d'Orsay [ISMO]
Rebarz, M. [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Sliwa, Michel [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Dumas, E. [Auteur]
Le Pleux, L. [Auteur]
Chimie Et Interdisciplinarité : Synthèse, Analyse, Modélisation [CEISAM]
Pellegrin, Y. [Auteur]
Odobel, F. [Auteur]
Mayer, C. R. [Auteur]
Titre de la revue :
Applied Surface Science
Nom court de la revue :
Appl. Surf. Sci.
Numéro :
499
Date de publication :
2019-12-28
ISSN :
0169-4332
Mot(s)-clé(s) en anglais :
Polypyridyl ruthenium complexes
Ag
Au
Nanoparticles
Spectroscopies
Electrochemistry
Ag
Au
Nanoparticles
Spectroscopies
Electrochemistry
Discipline(s) HAL :
Chimie/Chimie théorique et/ou physique
Résumé en anglais : [en]
The synthesis, reactivity and properties of a series of four polypyridyl ruthenium complexes have been studied. These complexes were used to post-functionalize preformed 3 nm silver and gold nanoparticles (NPs) in water ...
Lire la suite >The synthesis, reactivity and properties of a series of four polypyridyl ruthenium complexes have been studied. These complexes were used to post-functionalize preformed 3 nm silver and gold nanoparticles (NPs) in water and in dichloromethane (DCM). We studied the influence of the grafted complexes on the formation process and stability of the colloidal solutions and we investigated the optical and electrochemical properties of the final nanocomposites. Among the series of four ruthenium complexes, three novel heteroleptic complexes (1–3) bearing one pyridine, one amine or two carboxydithioic acid pendant groups were synthesized and reacted with preformed Au-NPs and Ag-NPs. Results were compared to those obtained with the model [Ru(bpy)3]2+ complex (4). The strength of the interaction between the anchoring group and the surface of NPs influenced the size, shape and stability of the final nanocomposites. Polar solvent such as water induced aggregation and lead to unstable nanocomposites. Stationary and time resolved luminescence of grafted nanocomposites (1–3) showed that the luminescence of complexes were completely quenched (lifetime and emission quantum yield) in water by electron transfer processes, moreover electrical measurements rationalize that Ag nanocomposites exhibit the stronger quenching due to a lower oxidation potential. It also showed a current enhancement associated with double layer charging of the metal nanoparticle cores.Lire moins >
Lire la suite >The synthesis, reactivity and properties of a series of four polypyridyl ruthenium complexes have been studied. These complexes were used to post-functionalize preformed 3 nm silver and gold nanoparticles (NPs) in water and in dichloromethane (DCM). We studied the influence of the grafted complexes on the formation process and stability of the colloidal solutions and we investigated the optical and electrochemical properties of the final nanocomposites. Among the series of four ruthenium complexes, three novel heteroleptic complexes (1–3) bearing one pyridine, one amine or two carboxydithioic acid pendant groups were synthesized and reacted with preformed Au-NPs and Ag-NPs. Results were compared to those obtained with the model [Ru(bpy)3]2+ complex (4). The strength of the interaction between the anchoring group and the surface of NPs influenced the size, shape and stability of the final nanocomposites. Polar solvent such as water induced aggregation and lead to unstable nanocomposites. Stationary and time resolved luminescence of grafted nanocomposites (1–3) showed that the luminescence of complexes were completely quenched (lifetime and emission quantum yield) in water by electron transfer processes, moreover electrical measurements rationalize that Ag nanocomposites exhibit the stronger quenching due to a lower oxidation potential. It also showed a current enhancement associated with double layer charging of the metal nanoparticle cores.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
CNRS
Collections :
Date de dépôt :
2024-02-28T23:17:40Z
2024-03-11T09:32:12Z
2024-03-11T09:32:12Z
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