“…Organic covalent functionalization reactions of graphene include two general routes: (a) the formation of covalent bonds between free radicals or dienophiles and C═C bonds of pristine graphene and (b) the formation of covalent bonds between organic functional groups and the oxygen groups of GO (Georgakilas et al, 2012). Characteristic of these processes are the presence of carbonyl, hydroxyl and carboxyl groups (resulting from the oxidation of graphite itself by the Hummers method); nevertheless, functional moieties, such as amines (Wanjeri et al, 2018;Bueno et al, 2017), amides (Ahmed and Kim, 2017;Mrlík et al, 2016), nitro (Begum et al, 2017), thio-compounds (Mahmoodi et al, 2017;Cai and Larese-Casanova, 2016), carbene cycloaddition (Zan, 2014), among others, can be chemically added to the carbon plane edges and surface. Within the covalent routes, a functionalizing group, such as thionyl, can replace the hydroxyl groups that form on the graphene surface after oxidation (Cai and Larese-Casanova, 2016).…”