Related Experiment Video
Updated: Sep 29, 2025

Microscopic Visualization of Porous Nanographenes Synthesized through a Combination of Solution and On-Surface Chemistry
Published on: March 4, 2021
Synthesis of octagon-containing molecular nanocarbons
Greco González Miera1, Satoshi Matsubara1, Hideya Kono1
1Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, Nagoya University Chikusa Nagoya 464-8602 Japan itami@chem.nagoya-u.ac.jp.
Abstract:
Nanocarbons, such as fullerenes, carbon nanotubes, and graphenes, have long inspired the scientific community. In order to synthesize nanocarbon molecules in an atomically precise fashion, many synthetic reactions have been developed. The ultimate challenge for synthetic chemists in nanocarbon science is the creation of periodic three-dimensional (3D) carbon crystals. In 1991, Mackay and Terrones proposed periodic 3D carbon crystals with negative Gaussian curvatures that consist of six- and eight-membered rings (the so-called Mackay-Terrones crystals). The existence of the eight-membered rings causes a warped nanocarbon structure. The Mackay-Terrones crystals are considered a "dream material", and have been predicted to exhibit extraordinary mechanical, magnetic, and optoelectronic properties (harder than diamond, for example). To turn the dream of having this wonder material into reality, the development of methods enabling the creation of octagon-embedding polycyclic structures (or nanographenes) is of fundamental and practical importance. This review describes the most vibrant synthetic achievements that the scientific community has performed to obtain curved polycyclic nanocarbons with eight-membered rings, building blocks that could potentially give access as templates to larger nanographenes, and eventually to Mackay-Terrones crystals, by structural expansion strategies.
Related Concept Videos
Carbon Skeletons
Hybridization of Atomic Orbitals II
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Frost Circles for Different Conjugated Systems
Exceptions to the Octet Rule
Radicals: Electronic Structure and Geometry
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...

