Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9577690 | Chemical Physics Letters | 2005 | 5 Pages |
Abstract
Heating [60]fullerene with Br2/FeCl3/benzene under reflux for 24 h yields in addition to the previously observed phenylated fullerenes, two bromine-containing open-cage products of 768/770 and 848 amu, each of which fragments to decacyclene during EI mass spectrometry. This provides an example of the reverse of the [60]fullerene synthesis from aromatic precursors.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Adam D. Darwish, Paul R. Birkett, G. John Langley, Roger Taylor,