Organometallic Complexes of Graphene
arXiv:1308.4924 · doi:10.1039/C0SC00634C
Abstract
We demonstrate the organometallic hexahapto complexation of chromium with graphene, graphite and carbon nanotubes. All of these extended periodic pi-electron systems exhibit some degree of reactivity toward the reagents CrCO)6 and (eta6-benzene)Cr(CO)3, and we are able to demonstrate the formation of (eta6-rene)Cr(CO)3 or (eta6-arene)2Cr, where arene = single-walled carbon nanotubes (SWNT), exfoliated graphene (XG), epitaxial graphene (EG) and highly-oriented pyrolytic graphite (HOPG). We find that the SWNTs are the least reactive presumably as a result of the effect of curvature on the formation of the hexahapto bond; in the case of HOPG, (eta6-HOPG)Cr(CO)3 was isolated while the exfoliated graphene samples were found to give both (eta6-graphene)2Cr, and (eta6-graphene)Cr(CO)3 structures. We report simple and efficient routes for the mild decomplexation of the graphene-chromium complexes which appears to restore the original pristine graphene state. This study represents the first example of the use of graphene as a ligand and is expected to expand the scope of graphene chemistry in connection with the application of this material in organometallic catalysis.
arXiv comment40 pages, 15 figures: comments are welcome
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- Organometallic Hexahapto Functionalization of Single Layer Graphene as a Route to High Mobility Graphene Devices
- Electrochemical Grafting of Naphthylmethyl Radicals to Epitaxial Graphene: A Versatile Platform to Reversibly Engineer the Band Structure and Transport Properties of Graphene
- Interlocking mechanism between molecular gears attached to surfaces