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  • Light-controlled morphologies of self-assembled triarylamine-fullerene conjugates.

Light-controlled morphologies of self-assembled triarylamine-fullerene conjugates.

ACS nano (2015-03-04)
Eric Busseron, Juan-José Cid, Adrian Wolf, Guangyan Du, Emilie Moulin, Gad Fuks, Mounir Maaloum, Prasad Polavarapu, Adrian Ruff, Ann-Kathrin Saur, Sabine Ludwigs, Nicolas Giuseppone
ABSTRACT

A family of triarylamine-fullerene conjugates has been synthesized and shown to self-assemble upon light stimulation in chlorinated solvents. This light-induced process primarily involves excitation of triarylamine derivatives, which then oxidize and stack with their neutral counterparts to form charge transfer complexes in the form of p-conducting channels, while fullerenes are consequently enforced in coaxial n-conducting columnar arrangements. These supramolecular heterojunctions can be organized over very long distances in micrometric fibers when a controlled amount of photons is provided from a white light source to initiate the process. Surprisingly, when sunlight or UV light is used instead, the nanostructuration leads to monodisperse spherical objects due to the nature of the nucleation-growth process involved in the stacks formation. This control over the supramolecular morphology of organic self-assemblies using the nature of light is of general interest for the design of functional responsive materials.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
3-(Benzyldimethylammonio)propanesulfonate, BioXtra, ≥99.0% (HPCE)
Sigma-Aldrich
Acetone-d6, 99.9 atom % D, contains 0.03 % (v/v) TMS
Sigma-Aldrich
Acetone-d6, 99.5 atom % D
Sigma-Aldrich
Acetone-d6, 99.9 atom % D, contains 1 % (v/v) TMS
Sigma-Aldrich
Acetone-d6, "100%", 99.95 atom % D
Sigma-Aldrich
Acetone-d6, 99.9 atom % D
Sigma-Aldrich
Acetone-d6, 99.9 atom % D