Issue 92, 2017

Non-covalent graphene nanobuds from mono- and tripodal binding motifs

Abstract

Graphene nanobuds were prepared via the non-covalent anchoring of C60-based molecules endowed with one or three pyrene units, respectively. TGA, FTIR, UV-Vis and TEM investigations confirmed the formation of nanohybrids. For the two molecular derivatives, striking differences were determined in their interaction with graphene or carbon surfaces by Raman, cyclic voltammetry and molecular mechanics calculations, revealing the important role of pyrene adsorption in modulating the electronic properties of the nanohybrids.

Graphical abstract: Non-covalent graphene nanobuds from mono- and tripodal binding motifs

Supplementary files

Article information

Article type
Communication
Submitted
10 Қаз. 2017
Accepted
20 Қаз. 2017
First published
20 Қаз. 2017

Chem. Commun., 2017,53, 12402-12405

Non-covalent graphene nanobuds from mono- and tripodal binding motifs

M. Garrido, J. Calbo, L. Rodríguez-Pérez, J. Aragó, E. Ortí, M. xmlns="http://www.rsc.org/schema/rscart38"> <. Á. Herranz and N. Martín, Chem. Commun., 2017, 53, 12402 DOI: 10.1039/C7CC07836F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements