On the Functionalization of C<sub>60</sub> with Vinylallenes Generated <i>in situ</i> by Rhodium Catalysis

Abstract The functionalization of fullerenes is important for several reasons, primarily related to enhancing their chemical reactivity, solubility, and potential of applications in optoelectronics and biomedicine. In this study, we present a novel approach to functionalize C 60 through a cascade process encompassing an unprecedented Rh‐catalyzed cycloisomerization of 1,6‐allenynes to in situ generate a vinylallene that is followed by a Diels‐Alder reaction with pristine fullerene, resulting in the formation of 6,6‐fused bicyclic fullerene derivatives. The mechanism governing this process was elucidated by DFT calculations and confirmed by deuterium labelling and control experiments, demonstrating the critical role of traces of water in the reaction medium to mediate the observed reactivity.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2024-10-06
DOI
https://doi.org/10.1002/adsc.202401163
Citations
2
Primary Topic
Fullerene Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.50

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article

On the Functionalization of C60 with Vinylallenes Generated in situ by Rhodium Catalysis

Albert Artigas, Anna Roglans, Miquel Solà, Anna Pla‐Quintana et al.
2 citations
Advanced Synthesis & Catalysis
Fullerene Chemistry and Applications
0.50
article

On the Functionalization of C60 with Vinylallenes Generated in situ by Rhodium Catalysis

Albert Artigas, Anna Roglans, Miquel Solà, Anna Pla‐Quintana, Cristina Castanyer
article en
2 citations

Abstract

Abstract The functionalization of fullerenes is important for several reasons, primarily related to enhancing their chemical reactivity, solubility, and potential of applications in optoelectronics and biomedicine. In this study, we present a novel approach to functionalize C 60 through a cascade process encompassing an unprecedented Rh‐catalyzed cycloisomerization of 1,6‐allenynes to in situ generate a vinylallene that is followed by a Diels‐Alder reaction with pristine fullerene, resulting in the formation of 6,6‐fused bicyclic fullerene derivatives. The mechanism governing this process was elucidated by DFT calculations and confirmed by deuterium labelling and control experiments, demonstrating the critical role of traces of water in the reaction medium to mediate the observed reactivity.

Advanced Synthesis & CatalysisVol. 367(4)
Universitat de Girona (ES)
Generalitat de Catalunya
Openalex Percentile: Top 39%
Fullerene Chemistry and Applications
0.50
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