NAKAMURA Functional Carbon Cluster

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Research Director: Dr. Eiichi Nakamura
Professor, School of Science, The University of Tokyo
Research Term 2004-2009

In the formation of life on Earth and its subsequent evolution, carbon has played a central role. This is especially due to its unique bonding capabilities, allowing a wide variety of molecules to form. It is for this reason that the area of chemistry dealing with carbon molecules came to be called organic chemistry, as opposed to inorganic chemistry. This separation was also originally made based on the idea that organic molecules have a special “vital force”, and cannot be made from inorganic ones. This was eventually proved to be totally incorrect in 1828 when urea was synthesized from an inorganic substance.

Benzene, a six-carbon ring, is a key molecule in the science of life, discovered in 1825 by Michael Faraday, a physicist and chemist. Although in the 19th century people were very interested in benzene, by its end this enthusiasm had vanished, along with a general feeling that there was nothing further to be learned from organic chemistry. Interest was later regained because of the resonance theory of quantum mechanics. Whereas before benzene was thought to involve a quickly equilibrating double bond, it was now understood to be a conjugated structure. Synthetic chemists subsequently found many interesting ways to add functionality to organic molecules, especially those involving benzene: catalysts, anti-inflationary materials, cancer fighting drugs, and a conducting polymer are examples. In the 20th century, benzene thus recovered its prime status in chemistry.

The Buckyball was discovered in 1985 (also called C60, C70 or fullerene, after Buckminister Fuller, an architect of geodesic domes). Whereas inorganic chemists see these fullerenes and later discovered nanotubes as interesting structures unrelated to life, organic chemists see huge clusters of benzene rings. These clusters can also be considered as polymers of benzene. Though a majority of people thought that fullerenes and nanotubes are interesting, Eiichi Nakamura thought that their organic derivatives would be much more interesting, since this was the case in the history of benzene. Nakamura started working on buckyballs in 1992, when they first became available in sufficient quantity. His group was among the first to use this new structure in synthetic chemistry. Nakamura immediately thought that if side-chain structures could be assembled to these clusters they might exhibit interesting functionality, such as drugs. One of the first functional molecules produced was an enzyme-like molecule in 1993 that had the ability to cut DNA.

In 1996 Nakamura succeeded to convert isotropic C60 into anisotropic C60. Using magnesium with a copper catalyst, it was possible to put 5 phenyl groups or 5 methyl groups at very specific regions of C60. Most importantly, the product was 100% pure and in 100% yield. This was the first and essentially the only reaction that converts C60 into organic C60. Using these handles, it was possible to attach the long side chains to methyl groups. Because C60 is essentially a round ball it is difficult to align for materials and functions. However, by considering a badminton shuttlecock, a molecular recognition was conceived where the ball part recognizes the feather part and aligns. These molecules were put together in one dimension in a crystalline material. This very unique structure shows possible use as a liquid-crystal material, which is being pursued.

In addition, Nakamura is also investigating a number of interesting and potentially functional materials. From a technological point of view, Nishi of Sony Corporation has been quoted as saying that in the past there were the ages of stone, bronze, iron and silicon; and that we are now entering the carbon age. Although carbon can never replace silicon, they are certainly complementary.

Outline of Research

 The Nakamura Functional Carbon Cluster project is aimed at creating a wide variety of functional materials based on C60 and carbon nanotubes that are given functionality through organic synthesis. Possibilities include molecular electronic devices, a solar battery, thin film transistors, and luminescence materials. Next generation electronics based on organic materials. The research strategy is emphasizing several research themes:

 The central theme is synthesis strategies. In order to make more complex materials it is absolutely necessary to develop even more sophisticated synthetic methodologies.

 To use C60 in biological applications, it must be dissolved in water. This has been achieved, which subsequently revealed very primitive biological activity. Observations have shown that it is possible to bind C60 onto linear DNA, causing it to be expressed in mammalian cells. This methodology might be a possible way to deliver DNA into mammalian cells, and thus useful for gene therapy, so as to produce a useful product.

 Functionalized C60 has an innate ability to form an entity so that if an anion is made out of it, which is dissolved in neutral water, it forms a bilayer inside water. Its inside is water and its outside is water, just like a living cell. A basic understanding of how this happens is still not available. This amazing new membrane is being analyzed theoretically and experimentally with an aim for applications.

 A d-pi system has been made with a carbon nanotube. Gadolinium (Gd) metal was placed onto the tip of a carbon nanotube. Using a special electron microscope, the Gd could be seen sitting on a tube-like structure. An effort is being made to make a microscopic system by which both the metal and carbon atoms can be seen clearly, thus allowing the chemistry to be understood better, thus allowing new functional materials to be developed.

 The most socially oriented aspect of this project is to find wide-ranging applications of the newly created functional molecules. An application of functional fullerenes to printable electronic devices will be an example of such an endeavor.

Project Headquarter

Phone: 03-3815-1551
Fax: 03-3815-1552

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