4.6 Article

Synthesis of Endohedral Metallofullerene Glycoconjugates by Carbene Addition

Journal

MOLECULES
Volume 16, Issue 11, Pages 9495-9504

Publisher

MDPI AG
DOI: 10.3390/molecules16119495

Keywords

chemical functionalization; La(2)@I(h)-C(80); carbohydrate; diazirine; glycoconjugate

Funding

  1. The Next Generation Super Computing Project (Nanoscience Project), Nanotechnology Support Project
  2. Ministry of Education, Culture, Sports, Science, and Technology of Japan [22000009]
  3. JST
  4. MICINN
  5. [20108001]
  6. [20245006]
  7. [22750030]
  8. [20036008]
  9. [20038007]
  10. Grants-in-Aid for Scientific Research [20108002, 22750030, 20108001, 20245006, 23750035] Funding Source: KAKEN

Ask authors/readers for more resources

Endohedral metallofullerene glycoconjugates were synthesized under mild conditions by carbene addition using appropriate glycosylidene-derived diazirine with La(2)@I(h)-C(80). NMR spectroscopic studies revealed that the glycoconjugate consists of two diastereomers of [6,6]-open mono-adducts. The electronic properties were characterized using Vis/NIR absorption spectroscopy and electrochemical measurements. This study demonstrates that glycosylidene carbene is useful to incorporate carbohydrate moieties onto endohedral metallofullerene surfaces.

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