Screening of the chemical reactivity of three different graphite sources using the formation of reductively alkylated graphene as a model reaction

Knirsch K, Englert J, Dotzer C, Hauke F, Hirsch A, Hauke F (2013)

Publication Language: English

Publication Type: Journal article, Original article

Publication year: 2013

Journal

Chemical Communications Royal Society of Chemistry

Original Authors: Knirsch K.C., Englert J.M., Dotzer C., Hauke F., Hirsch A.

Publisher: Royal Society of Chemistry

Book Volume: 49

Pages Range: 10811-10813

Journal Issue: 92

DOI: 10.1039/c3cc46621c

Abstract

Reductive alkylation of three graphite starting materials G(flake), G(powder), and G(spherical) reveals pronounced differences in the obtained covalently functionalized graphene with respect to the degree of functionalization, exfoliation efficiency and product homogeneity, as demonstrated by statistical Raman microscopy (SRM), TGA/MS, IR-spectroscopy and solubility behavior.This journal is © The Royal Society of Chemistry 2013.

Authors with CRIS profile

Kathrin Knirsch Lehrstuhl für Organische Chemie II Jan Englert Sonderforschungsbereich 953/3 Synthetische Kohlenstoffallotrope Christoph Dotzer Lehrstuhl für Organische Chemie II Frank Hauke Zentralinstitut für Neue Materialien und Prozesstechnik Andreas Hirsch Lehrstuhl für Organische Chemie II

How to cite

APA:

Knirsch, K., Englert, J., Dotzer, C., Hauke, F., Hirsch, A., & Hauke, F. (2013). Screening of the chemical reactivity of three different graphite sources using the formation of reductively alkylated graphene as a model reaction. Chemical Communications, 49(92), 10811-10813. https://dx.doi.org/10.1039/c3cc46621c

MLA:

Knirsch, Kathrin, et al. "Screening of the chemical reactivity of three different graphite sources using the formation of reductively alkylated graphene as a model reaction." Chemical Communications 49.92 (2013): 10811-10813.

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