Abstract
A trans-4-[60]fullerenobisacetic acid derivative was easily obtained from its diethyl ester, which was regio- and stereo-selectively prepared by the biscyclopropanation of [60]fullerene with a tethered bis(α-bromophenylacetate) derivative. The polycondensation of the resultant fullerenobisacetic acid with aromatic diamines proceeded smoothly to give the corresponding regio- and stereo-regular [60]fullerene pearl-necklace polyamides in excellent yields.
Original language | English |
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Pages (from-to) | 728-729 |
Number of pages | 2 |
Journal | Chemistry Letters |
Issue number | 7 |
DOIs | |
Publication status | Published - 2002 Jul 5 |
Externally published | Yes |
ASJC Scopus subject areas
- Chemistry(all)