| Title | Claisen rearrangement of graphite oxide: a route to covalently functionalized graphenes. |
| Publication Type | Journal Article |
| Year of Publication | 2011 |
| Authors | Collins, WR, Lewandowski, W, Schmois, E, Walish, J, Swager, TM |
| Journal | Angewandte Chemie, International Edition |
| Volume | 50 |
| Pagination | 8848–52 |
| Date Published | sep |
| ISSN | 1521-3773 |
| Keywords | functional group graphite oxide Claisen rearrangem |
| Abstract | The basal plane allylic alc. functionality of graphite oxide can be converted into N,N-dimethylamide groups through an Eschenmoser-Claisen sigmatropic rearrangement by using N,N-dimethylacetamide di-Me acetal. Subsequent sapon. of these groups affords the carboxylic acids, which, when deprotonated, electrostatically stabilize the graphene sheets in an aq. environment. [on SciFinder(R)] |
| URL | http://www.ncbi.nlm.nih.gov/pubmed/21826769 |
| DOI | 10.1002/anie.201101371 |