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I. Schéma, Synthèse de NCs à coeur huileux par le procédé couche-par-couche à partir de la surface d'une nano-gouttelette d'émulsion chargée positivement (adapté de la rérérence 73 )

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I. Schéma, Elaboration de NCs à coeur huileux par le procédé de polymérisation par étapes à l'interface d'une gouttelette de miniémulsion

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I. Schéma, Modification de D-glucose via une transformation « one-pot multi-step » impliquant la réaction de chimie « click

I. Schéma, Mécanisme proposé de la réaction CuAAC 179

I. Schéma, Réaction de chimie « click » CuAAC entre des alcynes terminaux et un nucléoside (1(4'-azido-2'-deoxy-2'-fluoro-?-D-arabinofuranosyl) cytosine) 180

I. Schéma, Réaction de chimie « click » CuAAC réalisée à l'interface entre deux solvant nonmiscibles et catalysée par CuSO4/NaAsc (inspiré par 183 )

I. Schéma, 22. Deux principaux mécanismes de la réaction thiol-ène: a) nucléophile ou basique, b) radicalaire

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I. Schéma, Mécanisme de la réaction thiol-ène catalysée par une base 187. B correspond à une base et EWG aux groupes attracteurs d'électrons (ang. Electron Withdrawing Groups)

I. Schéma, Mécanisme radicalaire de la réaction thiol-ène 190

I. Schéma, Mécanisme d'amorçage de la réaction thiol-ène en utilisant un photo-amorceur de type I, dans l'exemple du DMPA 189

I. Schéma, Mécanisme d'amorçage de la réaction thiol-ène en utilisant un photo-amorceur de type II

I. Schéma, Mécanisme de formation de radicaux par un système BPO/amine tertiaire 206

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I. I. Schéma, Synthèse du PLA ?-alcyne par polymérisation par ouverture de cycle du D,L-lactide catalysée par SnOct2 et amorcée par l'alcool propargylique

I. I. Schéma, Synthèse du PLA ?-SH : I) Synthèse du PLA-SS-PLA par polymérisation par ouverture de cycle du D,L-lactide, II) Réduction des liaisons disulfure en thiol

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I. I. Schéma, Réduction d'une liaison disulfure à l'aide du DTT 13

I. I. Schéma, Synthèse du dextrane-azide (DexN3) par réaction entre le dextrane natif et l'acide 6-azidohexanoïque activé

I. I. Schéma, Synthèse du dextrane-méthacrylate (DexC=C) par réaction entre le dextrane natif et l'anhydride méthacrylique

I. I. Schéma, Synthèse du dextrane-alcène (DexC6C=C) par réaction entre le dextrane natif et l'acide 5-hexenoïque activé, vol.8

I. I. Schéma, émulsion-évaporation de solvant couplé à une réaction de chimie « click » à l'interface de l'émulsion huile-dans-eau, Synthèse des NCs de PLA à coeur M810 et recouvertes de dextrane par le procédé d

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I. I. Schéma, 11. Réaction « click » thiol-ène nucéophile entre un DexC=C et un PLA ?-SH

I. I. Schéma, 12. Réaction « click » thiol-ène entre un DexC6C=C et un PLA ?-SH dans les conditions radicalaires

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I. Schéma, Synthèse du PLA ?-alcyne par polymérisation par ouverture de cycle du D,L-lactide catalysée par SnOct2 et amorcée par l'alcool propargylique

I. Schéma, Synthèse du PLA-SS-PLA par polymérisation par ouverture de cycle du D,L-lactide catalysée par SnOct2 et amorcée par le 2-hydroxyéthyl disulfide

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I. Schéma, Réaction du dextrane avec l'anhydride méthacrylique

I. Schéma, Synthèse de l'ester activé de l'acide hex-5-énoïque, vol.8

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I. Schéma, Préparation des NSs ou des NCs par le procédé d'émulsion-évaporation de solvant couplé à une réaction de chimie « click » CuAAC en utilisant différents catalyseurs: a) CuBr ou CuI, b) CuSO4 (±BPMODA)/AAsc

I. Schéma, Préparation des NSs ou des NCs par le procédé d'émulsion-évaporation de solvant couplé à une réaction de chimie « click » thiol-ène dans des conditions nucléophiles

I. Schéma, Préparation des NSs par le procédé d'émulsion-évaporation de solvant couplé à une réaction de chimie « click » thiol-ène dans les conditions radicalaires

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