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A Diaminoterephthalate-C-60 Dyad: A New Material for Optoelectronic Applications

Academic Article
Publication Date:
2015
abstract:
Diaminoterephthalate was used for the first time as a chromophore in a dyad with [60]fullerene. The synthesis was accomplished from the benzyl methyl diester by hydrogenolytic cleavage of the benzyl group, re-esterification with a benzyl alcohol with protected formyl function, deprotection of the latter and final 1,3-dipolar cycloaddition with C-60 and sarcosine via the azomethine ylide.
Iris type:
01.01 Articolo in rivista
Keywords:
diaminoterephthalate; 1; 3-dipolar cycloaddition; dyad; esterification; fullerene
List of contributors:
Rozzi, CARLO ANDREA
Authors of the University:
ROZZI CARLO ANDREA
Handle:
https://iris.cnr.it/handle/20.500.14243/292033
Published in:
SYNTHESIS (STUTTG.)
Journal
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