Preparation of chiral graphene oxides by covalent attachment of chiral cysteines for voltammetric recognition of tartrates.

The authors describe the preparation of a chiral graphene oxides (GOs) by covalent attachment of D- or L-cysteine using a one-step hydrothermal method. The resulting chiral functionalized GOs shows circular dichroism with intensities similar to those produced by the cysteines. This indicates that the chirality of cysteines is well preserved in the chiral GOs. The material is reasonably stable at temperatures from 20 to 200 °C and at pH values from 0 to 14. A glassy carbon electrode (GCE) was modified with the chiral GOs and then tested for recognition capability for L- and D-tartrate (0.5 mM). The enantioselectivity of the chiral GOs appears to be the result of a synergistic effect where GO increases the conductivity and cysteine provides the chiral environment. The method is assumed to provide a useful general scheme for development of advanced carbonaceous materials with chiral recognition capabilities. Graphical abstract Chiral graphene oxides produced by covalently attaching chiral amino acids displays effective enantioselective recognition. Graphical abstract contains poor quality of text inside the artwork. Please do not re-use the file that we have rejected or attempt to increase its resolution and re-save. It is originally poor, therefore, increasing the resolution will not solve the quality problem. We suggest that you provide us the original format. We prefer replacement figures containing vector/editable objects rather than embedded images. Preferred file formats are eps, ai, tiff and pdf.We have uploaded the modified version as Graphical abstract.