4.6 Article

The Impact of Copper-Catalyzed Alkyne-Azide 1,3-Dipolar Cycloaddition in Fullerene Chemistry

期刊

CHEMICAL RECORD
卷 15, 期 1, 页码 31-51

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/tcr.201402081

关键词

bioactive molecules; click chemistry; fullerene; photochemistry; synthetic methodology

资金

  1. University of Strasbourg
  2. CNRS
  3. Agence National de la Recherche Scientifique (ANR)
  4. International Center for Frontier Research in Chemistry (icFRC)
  5. LabEx Chimie des Systemes Complexes

向作者/读者索取更多资源

Click reactions largely cross the borders of organic synthetic chemistry and are now at the forefront of many interdisciplinary studies at the interfaces between chemistry, physics, and biology. As part of this research, our group is involved in a program on the development of clickable fullerene building blocks and their application in the preparation of a large variety of new advanced materials and bioactive compounds. Importantly, the introduction of the click chemistry concept in fullerene chemistry allowed us to produce compounds that would barely be accessible by using the classical tools of fullerene chemistry. This is particularly the case for the conjugation of fullerenes with other carbon nanoforms, such as carbon nanohorns and graphene. It is also the case for most of the sophisticated molecular ensembles constructed from clickable fullerene hexa-adduct building blocks. In this paper, we have summarized our ongoing progress in this particular field.

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