4.7 Article

Reversible Diels-Alder Addition to Fullerenes: A Study of Dimethylanthracene with H2@C60

Journal

NANOMATERIALS
Volume 12, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/nano12101667

Keywords

H-1 NMR spectroscopy; Diels-Alder reaction; 9; 10-dimethylanthracene; fullerene; H-2@C-60

Funding

  1. National Natural Science Foundation of China [21975288]
  2. Hunan Reaserch Founding [2020JJ4683]
  3. Changsha Research Founding [2014121]
  4. Shenzhen Research Founding [JCYJ20190806144616528]

Ask authors/readers for more resources

The study investigates the unique environment provided by studying isolated atoms or molecules within a fullerene cavity. The research focuses on the Diels-Alder addition reaction between 9,10-dimethyl anthracene and H-2@C-60, and characterizes the reaction using H-1 NMR spectroscopy.
The study of isolated atoms or molecules inside a fullerene cavity provides a unique environment. It is likely to control the outer carbon cage and study the isolated species when molecules or atoms are trapped inside a fullerene. We report the Diels-Alder addition reaction of 9,10-dimethyl anthracene (DMA) to H-2@C-60 while H-1 NMR spectroscopy is utilized to characterize the Diels-Alder reaction of the DMA with the fullerene. Through H-1 NMR spectroscopy, a series of isomeric adducts are identified. The obtained peaks are sharp, precise, and straightforward. Moreover, in this paper, H-2@C-60 and its isomers are described for the first time.

Authors

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

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available