Electroactive carbon nanoforms: A comparative study via sequential arylation and click chemistry reactions

Mateos-Gil J, Rodriguez-Perez L, Moreno-Oliva M, Katsukis G, Romero-Nieto C, Angeles Herranz M, Guldi DM, Martin N (2015)


Publication Type: Journal article

Publication year: 2015

Journal

Book Volume: 7

Pages Range: 1193-1200

Journal Issue: 3

DOI: 10.1039/c4nr04365k

Abstract

The reactivity of several carbon nanoforms (CNFs), single-walled carbon nanotubes (SWCNTs), multi-walled carbon nanotubes (MWCNTs) and graphene, has been investigated through a combination of arylation and click chemistry CuI-mediated azide-alkyne cycloaddition (CuAAC) reactions. The approach is based on the incorporation of electroactive π-extended tetrathiafulvalene (exTTF) units into the triazole linkers to modulate the electronic properties of the obtained conjugates. The introduction of strain, by bending the planar graphene sheet into a 3D carbon framework, is responsible for the singular reactivity observed in carbon nanotubes. The formed nanoconjugates were fully characterized by analytical, spectroscopic, and microscopic techniques (TGA, FTIR, Raman, UV-Vis-NIR, cyclic voltammetry, TEM and XPS). In the case of SWCNT conjugates, where the functionalization degree is higher, a series of steady-state and time resolved spectroscopy experiments revealed a photoinduced electron transfer from the exTTF unit to the electron-accepting SWCNT.

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APA:

Mateos-Gil, J., Rodriguez-Perez, L., Moreno-Oliva, M., Katsukis, G., Romero-Nieto, C., Angeles Herranz, M.,... Martin, N. (2015). Electroactive carbon nanoforms: A comparative study via sequential arylation and click chemistry reactions. Nanoscale, 7(3), 1193-1200. https://doi.org/10.1039/c4nr04365k

MLA:

Mateos-Gil, Jaime, et al. "Electroactive carbon nanoforms: A comparative study via sequential arylation and click chemistry reactions." Nanoscale 7.3 (2015): 1193-1200.

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