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Synthesis of the First Tetracene‐[60]fullerene Dyad
Author(s) -
Taillemite Sébastien,
Fichou Denis
Publication year - 2004
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200400506
Subject(s) - tetracene , chemistry , dyad , fullerene , aromaticity , stereochemistry , photochemistry , anthracene , organic chemistry , molecule , psychology , social psychology
We report on a multistep synthesis of the newly designed tetracene‐[60]fullerene dyad involing a Bingel reaction between the tetracene and C 60 moieties. This strategy prevents the usual Diels−Alder reaction which would result in the loss of the tetracene aromaticity in the target dyad. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)
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