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An aromatic micelle with bent pentacene-based panels: encapsulation of perylene bisimide dyes and graphene nanosheets.


ABSTRACT: For exploitation of a new class of aromatic micelles, we synthesized a bent pentacene-based amphiphilic molecule through Diels-Alder reaction. The amphiphiles bearing two trimethylammonium tethers assemble into a spherical aromatic micelle, with an average core diameter of 1.5 nm, in water at room temperature. The new aromatic micelle efficiently encapsulates perylene bisimide (PBI) dyes and graphene nanosheets (GNS) in water. The encapsulated PBI dyes form a parallel stacked dimer, exhibiting characteristic absorption and emission bands. In addition, the encapsulated GNS are composed of few-layer graphene sheets with an average lateral size of ?7 nm, as confirmed by Raman spectroscopy. The resultant, aqueous host-guest complexes are stable even after three weeks in water under ambient conditions.

SUBMITTER: Ito K 

PROVIDER: S-EPMC7472825 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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An aromatic micelle with bent pentacene-based panels: encapsulation of perylene bisimide dyes and graphene nanosheets.

Ito Kenta K   Nishioka Tomoya T   Akita Munetaka M   Kuzume Akiyoshi A   Yamamoto Kimihisa K   Yoshizawa Michito M  

Chemical science 20200605 26


For exploitation of a new class of aromatic micelles, we synthesized a bent pentacene-based amphiphilic molecule through Diels-Alder reaction. The amphiphiles bearing two trimethylammonium tethers assemble into a spherical aromatic micelle, with an average core diameter of 1.5 nm, in water at room temperature. The new aromatic micelle efficiently encapsulates perylene bisimide (PBI) dyes and graphene nanosheets (GNS) in water. The encapsulated PBI dyes form a parallel stacked dimer, exhibiting c  ...[more]

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