Article ID Journal Published Year Pages File Type
9577690 Chemical Physics Letters 2005 5 Pages PDF
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
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