| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1415740 | Carbon | 2011 | 4 Pages |
Acid–base titrations were used to assess the covalent reactivity of carboxylic groups on single-layer graphene oxides (SLGO) or hydrazine-reduced analogues (SLGR) when treated with thionyl chloride and subsequent coupling to amines. Reflux with aggressive solvents led to size reduction and folding of individual sheets as well as loss of carboxylic groups, substantially so for SLGR. Room temperature treatment of SLGO with a carbodiimide collapsed the sheets into star-like clusters, which exhibited poor subsequent reactivity with amines. Ultimately, conventional chemical treatment of carboxylic groups on SLGO leads to morphological changes and reduced reactivity, which may potentially limit their use.
Graphical abstractConventional chemical treatment of carboxylic groups on single-layer graphene oxides leads to dramatic structural changes that directly affects their chemical reactivity and potential end use.Figure optionsDownload full-size imageDownload as PowerPoint slideResearch highlights► Single-layer graphene oxide changes shape under chemical treatment limiting its reactivity. ► Carbodiimide reactions led to star-like clusters of single-layer graphene oxide. ► Thionyl chloride reactions led to sheet size reduction and folding of single-layer graphene oxide. ► Hydrazine reactions weakens single-layer graphene oxide, potentially limiting further chemistry.
