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'Zipping-up' rings to make nanographenes

(Nanowerk News) Nanographenes are attracting wide interest from many researchers as a powerful candidate for the next generation of carbon materials due to their unique electric properties. Scientists at Nagoya University have now developed a fast way to form nanographenes in a controlled fashion. This simple and powerful method for nanographene synthesis could help generate a range of novel optoelectronic materials, such as organic electroluminescent displays and solar cells.
A group of chemists of the JST-ERATO Itami Molecular Nanocarbon Project and the Institute of Transformative Bio-Molecules (ITbM) of Nagoya University, and their colleagues have developed a simple and powerful method to synthesize nanographenes. This new approach, recently described in the journal Science ("Synthesis of partially and fully fused polyaromatics by annulative chlorophenylene dimerization"), is expected to lead to significant progress in organic synthesis, materials science and catalytic chemistry.
nanographene synthesis by zipping up partially fused aromatics
A new method for nanographene synthesis by zipping up partially fused aromatics. Gray colored balls represent carbon atoms and gray colored sticks represent chemical bonds. (Image: Nagoya University)
Nanographenes, one-dimensional nanometer-wide strips of graphene, are molecules composed of benzene units. Nanographenes are attracting interest as a powerful candidate for next generation materials, including optoelectronic materials, due to their unique electric characteristics. These properties of nanographenes depend mainly on their width, length and edge structures. Thus, efficient methods to access structurally controlled nanographenes is highly desirable.
The ideal synthesis of nanographenes would be a ‘LEGO’-like assembly of benzene units to define the exact number and shape of the molecule. However, this direct approach is currently not possible. The team developed an alternative method that is simple and controls the nanographene structure as it forms in three key steps.
First, simple benzene derivatives are assembled linearly, through a cross-coupling reaction. Then, these benzene chains are connected to each other by a palladium catalyst that leads to a molecule with three benzene rings bound together in a flat, triangle-like shape. This process repeats all the way up the chain, effectively zipping up the rings together.
Strategies to synthesize nanographene
Strategies to synthesize nanographene. A new synthetic approach for nanographenes from simple benzene derivatives via cross-coupling reactions and Scholl reactions. (Image: Nagoya University)
The innovation the team developed was a new way to achieve the middle step that forms the three-ring triangle-like unit that forms the core for further reactions to generate the nanographene molecule. A classic technique to connect benzene units uses aryl halides as reaction reagents. Aryl halides are aromatic compounds in which one or more hydrogen atoms bonded to an aromatic ring are replaced by halogen atoms such as fluorine (F), chlorine (Cl), bromine (Br), or iodine (I). This allows benzene to connect at a single point through a process called dimerization, which was discovered by Fritz Ullmann and Jean Bielecki in 1901. However, the Ullmann reaction does not generate nanographenes when using the compound phenylene as the starting material.
The team discovered that using a palladium catalyst enabled connections between benzene units at two points, providing the triangle-like structure of three benzene rings. A triphenylene moiety is formed in the center of each group of rings.
“This discovery was quite accidental,” says Designated Associate Professor Kei Murakami, a chemist at Nagoya University and one of the leaders of this study. “We think that this reaction is the key of this new approach for nanographene synthesis.”
The team then utilized a process called the Scholl reaction to repeat this process and successfully synthesize a nanographene molecule. The reaction proceeds in a similar manner to benzene rings being zipped up, with the triphenylene moiety acting as the core.
“One of the most difficult parts of this research was obtaining scientific evidence to prove the structures of the triphenylene derivative and nanographene molecules,” says Yoshito Koga, a graduate student who mainly conducted the experiments. “Since no one in our group has ever handled triphenylenes and nanographenes before, I was conducting the research through a ‘trial and error’ manner. I was extremely excited when I first saw the mass spectrometry signal of the desired molecule to reveal the mass of the molecule through MALDI (Matrix Assisted Laser Desorption/Ionization), which indicated that we had actually succeeded in making nanographene in a controlled fashion.”
synthetic approach towards nanographenes from phenylene
A new synthetic approach towards nanographenes from phenylene: (a) annulative dimerization of phenylene to triphenylene; (b) Scholl reaction "zips up" molecules to make nanographenes. (Image: Nagoya University)
The team had already succeeded in synthesizing various triphenylene derivatives, such as molecules including 10 benzene rings, naphthalene (a fused pair of benzene rings), nitrogen atoms, and sulfur atoms. These unprecedented triphenylene derivatives could potentially be used in solar cells.
“The approach for creating functional molecules from simple benzene units will be applicable to the synthesis of not only nanographene, but also to various other nanocarbon materials,” says Murakami.
“Nanographenes are bound to be useful as future materials,” says Professor Kenichiro Itami, director of the JST-ERATO Itami Molecular Nanocarbon Project. “We hope that our discovery will lead to the acceleration of applied research and advance the field of nanographene science.
Source: Institute of Transformative Bio-Molecules, Nagoya University