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, Résultats et discussions
, Leur propension à s'auto-assembler (?-? stacking) et leur propriétés spectroscopiques déjà bien connues en font un système plus qu'indiqué pour l'élaboration d'objets supramoléculaires dissipatifs. 9 Au cours de ces trois années, nous avons donc usé de divers stimulus, Les Perylènes diimides (PDIs) sont des briques moléculaires de choix en chimie supramoléculaire
, Ce dernier peut facilement être réduit en dianion (PDI-1 2-) en présence de dithionite (Na2S2O4, Figure 3A). PDI-1 peut aisément être dissout dans une solution tampon borate en une solution rouge. L'agrégation de PDI-1 en objets colloïdaux a pu être mise en évidence par UV-Vis et microscopie confocale (ces agrégats précipitent en 12h). Lors de la réduction sous addition de dithionite, Un dérivé de perylène diimide (PDI-1) soluble dans l'eau a d'abord dû être synthétisé
Une exposition à l'air libre de la solution de PDI-1 2-permet de l'oxyder et d'y retrouver l'espèce neutre (Figure 3A). Il a ensuite été décidé d'étudier l'effet d'un cycle redox sur la structure de l'assemblage supramoléculaire (Figure 3B) ,
, Ces résultats sont caractéristiques d'une polymérisation supramoléculaire auto-catalytique (après un cycle redox, Figure 3C)). Forts de ce constat, il a ensuite été décidé d'évaluer l'effet de plusieurs cycles redox successifs sur le système supramoléculaire. Pour ce faire, la croissance autocatalytique de PDI-1 a été suivie par diffusion dynamique de la lumière (DLS) et par UV-Vis après chaque cycle redox (7 cycles espacés de 20 minutes chacun), Cette hypothèse a pu être vérifiée en effectuant un ensemencement d'une solution fraîche de PDI-1 avec d'autres ayant subi un cycle redox (1 heure après), ensemencement à l'issue duquel le temps de latence a pu être diminué de façon significative (caractéristique des systèmes auto-catalytiques)
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