Local curvature as a reactivity index of fullerene molecules in the cycloaddition reactions

Using the density-functional theory computations, the curvature features of fullerenes C20 (Ci), C24 (D6), C30-3 (C2v), C40 (D2), C60 (Ih), C70 (D5h), and C76 (D2) were studied as well as their cycloaddition reactions with various substrates (carbene, nitrene, azomethine ylide, and hydrogen azide). Linear correlations were found between the curvature indices of the reaction centers in the fullerene molecules and the computed heat effects of cycloaddition reactions. These correlations have a general nature, allow considering the reactivity of the fullerenes as a whole class of compounds, and take into account the nature of the reaction centers of fullerenes, features of the attached addend, and type of the reaction. The rule was deduced from the correlations about the reactivity of fullerenes toward two reactants, Y1 and Y2: if the reaction proceeds according to the same mechanism and one fullerene is known to be more reactive toward Y1 then other representatives of the fullerene family also exhibit greater reactivity toward Y1.

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Publication Details

Journal
Fullerenes Nanotubes and Carbon Nanostructures
Published
2026-06-29
DOI
https://doi.org/10.1080/1536383x.2026.2694548
Primary Topic
Fullerene Chemistry and Applications
Type
article
Field-Weighted Citation Impact
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article

Local curvature as a reactivity index of fullerene molecules in the cycloaddition reactions

Denis Sh. Sabirov, Igor S. Shepelevich, Ralia Shayakhmetova
Fullerenes Nanotubes and Carbon Nanostructures
Fullerene Chemistry and Applications
article

Local curvature as a reactivity index of fullerene molecules in the cycloaddition reactions

Denis Sh. Sabirov, Igor S. Shepelevich, Ralia Shayakhmetova
article en

Abstract

Using the density-functional theory computations, the curvature features of fullerenes C20 (Ci), C24 (D6), C30-3 (C2v), C40 (D2), C60 (Ih), C70 (D5h), and C76 (D2) were studied as well as their cycloaddition reactions with various substrates (carbene, nitrene, azomethine ylide, and hydrogen azide). Linear correlations were found between the curvature indices of the reaction centers in the fullerene molecules and the computed heat effects of cycloaddition reactions. These correlations have a general nature, allow considering the reactivity of the fullerenes as a whole class of compounds, and take into account the nature of the reaction centers of fullerenes, features of the attached addend, and type of the reaction. The rule was deduced from the correlations about the reactivity of fullerenes toward two reactants, Y1 and Y2: if the reaction proceeds according to the same mechanism and one fullerene is known to be more reactive toward Y1 then other representatives of the fullerene family also exhibit greater reactivity toward Y1.

Fullerenes Nanotubes and Carbon Nanostructures
Institute of Catalysis and Petrochemistry (RU)
Openalex Percentile: Top 13%
Fullerene Chemistry and Applications
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