Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Nov 16;59(47):20767-20778.
doi: 10.1002/anie.202006932. Epub 2020 Oct 19.

Graphene Oxide as a Mediator in Organic Synthesis: a Mechanistic Focus

Affiliations
Review

Graphene Oxide as a Mediator in Organic Synthesis: a Mechanistic Focus

Lorenzo Lombardi et al. Angew Chem Int Ed Engl. .

Abstract

Graphene oxide (GO) is experiencing growing interest by synthetic organic chemists as a promoter of chemical transformations. The synergistic role of the multiple functionalities featuring the nanostructured carbon materials and their π-domains enables the interplay of specific activation modes towards organic compounds that can explore unprecedented chemical modifications. A detailed comprehension of the mechanistic details that govern the transformations guided by GO is a not fully solved task in the field. In this direction, more sophisticated and diversified techniques are employed, providing insights towards intriguing activation modes exerted by the π-matrix and the oxygenated/sulfonate groups decorating the functionalized nano-carbon material. The present Minireview accounts for a critical survey of the most recent developments in the area of GO-mediated organic transformations with a specific focus on mechanist aspects.

Keywords: catalysis; graphene oxide; organic synthesis; reaction mechanism; selectivity.

PubMed Disclaimer

Similar articles

Cited by

References

    1. L. Dai, in Carbon-Based Metal-Free Catalysts: Design and Applications, Wiley-VCH, Weinheim, 2019.
    1. General reviews on carbocatalysis:
    1. D. R. Dreyer, C. W. Bielawski, Chem. Sci. 2011, 2, 1233-1240;
    1. D. Haag, H. H. Kung, Top. Catal. 2014, 57, 762-773;
    1. C. K. Chua, M. Pumera, Chem. Eur. J. 2015, 21, 12550-12562;

LinkOut - more resources