Related Experiment Video
Updated: May 11, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Synthesis and properties of confined carbyne and beyond
1State Key Laboratory of Optoelectronic Materials and Technologies, Guangdong Basic Research Center of Excellence for Functional Molecular Engineering, Nanotechnology Research Center, School of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, PR China.
Abstract:
Carbyne, a one-dimensional carbon allotrope characterized by sp1 hybridization, has attracted significant attention due to its unique structure and exceptional properties. In principle, carbyne is an infinite linear carbon chain, or a long linear carbon chain that its properties remain independent of its length. Despite being proposed a century ago, the existence of carbyne has been a subject of controversy, primarily because of its extreme instability and strong chemical reactivity. So far the longest end-capped polyyne and the carbon nanotube-confined linear carbon chain comprise up to 68 and 6000 carbon atoms, respectively. In this review, general synthesis methods for confined linear carbon chains, i.e., confined carbyne, are outlined, with a particular focus on the chronological development of routes towards carbyne. In addition, the structure and properties of the carbon chains unraveled by theoretical calculations and various Raman spectroscopy are discussed in detail. Finally, the current challenges in the synthesis and property-engineering of sp1-hybridized carbon but not limited to confined carbyne are addressed, offering insights into potential future directions for both fundamental research and applications.
Related Concept Videos
Conformations of Cyclohexane
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
Chair Conformation of Cyclohexane
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
Structure of Conjugated Dienes
Conjugated dienes are compounds characterized by the presence of alternating double and single bonds. In a conjugated system like 1,3-butadiene, the unhybridized 2p orbital on each carbon overlaps continuously, allowing the π electrons to be delocalized across the entire molecule. In contrast, this type of overlap does not occur in cumulated and isolated dienes, such as 2,3-pentadiene and 1,4-pentadiene, respectively. Instead, the π electrons remain localized between the...
Carbocations
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
Conformations of Cycloalkanes

