The Growth–Decay Mechanism: A Universal Pathway for Cyclocarbon Fusion

Cyclocarbons constitute a fundamental class of carbon allotropes with unique electronic properties. The recently synthesized C 13 provides a crucial model system for understanding odd-numbered cyclocarbons as experimental evidence confirms its dimerization into C 26 . The underlying mechanism remains unknown, while understanding it is crucial for the synthesis and storage of cyclocarbons. Here, we combine density functional theory with ab initio molecular dynamics simulations to systematically investigate C 13 dimerization. Our results identify electronic structures of diverse weakly bound configurations and reveal a nearly barrierless pathway for covalent bond formation of monomers. The reaction proceeds through a general growth–decay mechanism via bridgehead-ring intermediates, ultimately leading to C 26 . Furthermore, we demonstrate that atomic-scale manipulation of these intermediates may enable the controlled synthesis of various cyclocarbons, including C 7, C 9, C 11, C 15, C 17, and C 19 . This work provides essential mechanistic insights into cyclocarbon reactivity and establishes a viable bottom-up strategy for the construction of carbon-based nanostructures.

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Publication Details

Journal
Inorganic Chemistry
Published
2026-06-19
DOI
https://doi.org/10.1021/acs.inorgchem.6c00517
Primary Topic
Origins and Evolution of Life
Type
article
Field-Weighted Citation Impact
0.00

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article

The Growth–Decay Mechanism: A Universal Pathway for Cyclocarbon Fusion

Jialu Chen, Bin Jiang, Rongxing He
Inorganic Chemistry
Origins and Evolution of Life
article

The Growth–Decay Mechanism: A Universal Pathway for Cyclocarbon Fusion

Jialu Chen, Bin Jiang, Rongxing He
article en

Abstract

Cyclocarbons constitute a fundamental class of carbon allotropes with unique electronic properties. The recently synthesized C 13 provides a crucial model system for understanding odd-numbered cyclocarbons as experimental evidence confirms its dimerization into C 26 . The underlying mechanism remains unknown, while understanding it is crucial for the synthesis and storage of cyclocarbons. Here, we combine density functional theory with ab initio molecular dynamics simulations to systematically investigate C 13 dimerization. Our results identify electronic structures of diverse weakly bound configurations and reveal a nearly barrierless pathway for covalent bond formation of monomers. The reaction proceeds through a general growth–decay mechanism via bridgehead-ring intermediates, ultimately leading to C 26 . Furthermore, we demonstrate that atomic-scale manipulation of these intermediates may enable the controlled synthesis of various cyclocarbons, including C 7, C 9, C 11, C 15, C 17, and C 19 . This work provides essential mechanistic insights into cyclocarbon reactivity and establishes a viable bottom-up strategy for the construction of carbon-based nanostructures.

Inorganic Chemistry
University of Science and Technology of China (CN), Southwest University (CN), Ministry of Education (RO)
Southwest University
Openalex Percentile: Top 7%
Origins and Evolution of Life
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