4.6 Article

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

Journal

CHEMICAL RECORD
Volume 15, Issue 1, Pages 31-51

Publisher

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

Keywords

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

Funding

  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

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available