Issue 58, 2018
From the journal:

RSC Advances

The chemical functionalization of graphene nanoplatelets through solvent-free reaction†

Eunice Cunha, ORCID logo ‡*a   He Ren,‡b   Fei Lin,a   Ian A. Kinloch, ORCID logo a   Quanji Sun,b   Zhaodong Fan*b  and  Robert J. Young ORCID logo a  

* Corresponding authors

a National Graphene Institute and School of Materials, University of Manchester, Manchester M13 9PL, UK
E-mail: eunice.cunha-2@manchester.ac.uk

b Beijing Institute of Aeronautical Materials (BIAM), Beijing, China
E-mail: fanzhaodong99@sohu.com

Abstract

Graphene nanoplatelets (GNPs) were functionalized through 1,3-dipolar cycloaddition of azomethine ylide using a solvent-free approach and under different reaction conditions. The yield and the functionality of the carboxyl-terminated pyrrolidine ring attached on the surface of GNPs could be affected by varying the reaction temperature as well as the reactant to GNP weight ratio. The functionalized GNPs were characterized extensively using a range of spectroscopic and microscopy techniques.

Graphical abstract: The chemical functionalization of graphene nanoplatelets through solvent-free reaction

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Article information

DOI
https://doi.org/10.1039/C8RA04817G
Article type
Paper
Submitted
06 jun 2018
Accepted
21 set 2018
First published
28 set 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 33564-33573

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The chemical functionalization of graphene nanoplatelets through solvent-free reaction

E. Cunha, H. Ren, F. Lin, I. A. Kinloch, Q. Sun, Z. Fan and R. J. Young, RSC Adv., 2018, 8, 33564 DOI: 10.1039/C8RA04817G

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