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(Redirected from C60)
''"C60", "C-60" and "Buckyballs" redirect here.''
The 'fullerenes', discovered in 1985 by researchers at the University of Sussex and Rice University, are a family of carbon allotropes named after Richard Buckminster Fuller and are sometimes called 'buckyballs'. They are molecules composed entirely of carbon, in the form of a hollow sphere, ellipsoid, or tube. Cylindrical fullerenes are called carbon nanotubes or 'buckytubes'. Fullerenes are similar in structure to graphite, which is composed of a sheet of linked hexagonal rings, but they contain also pentagonal (or sometimes heptagonal) rings that prevent the sheet from being planar.
In molecular beam experiments, discrete peaks were observed corresponding to molecules with the exact mass of sixty or seventy or more carbon atoms. In 1985, Harold Kroto (then of the University of Sussex, now of Florida State University), James R. Heath, Sean O'Brien, Robert Curl and Richard Smalley, from Rice University, discovered C60, and shortly thereafter came to discover the fullerenes. Kroto, Curl, and Smalley were awarded the 1996 Nobel Prize in Chemistry for their roles in the discovery of this class of compounds. C60 and other fullerenes were later noticed occurring outside the laboratory (e.g., in normal candle soot). By 1991, it was relatively easy to produce gram-sized samples of fullerene powder using the techniques of Donald Huffman and Wolfgang Krätschmer. Fullerene purification remains a challenge to chemists and to a large extent determines fullerene prices. So-called endohedral fullerenes have ions or small molecules incorporated inside the cage atoms. Fullerene is an unusual reactant in many organic reactions such as the Bingel reaction discovered in 1993.
The existence of C60 was predicted in 1970 by Eiji Osawa of Toyohashi University of Technology. He noticed that the structure of a corannulene molecule was a subset of a soccer-ball shape, and he made the hypothesis that a full ball shape could also exist. His idea was reported in Japanese magazines, but did not reach Europe or America.
Buckminsterfullerene (C60) was named after Richard Buckminster Fuller, a noted architect who popularized the geodesic dome. Since buckminsterfullerenes have a similar shape to that sort of dome, the name was thought to be appropriate. As the discovery of the fullerene family came ''after'' buckminsterfullerene, the name was shortened to illustrate that the latter is a type of the former.
''For illustrations of geodesic dome structures, see Montreal Biosphere, Eden Project, Missouri Botanical Gardens, Science World at TELUS World of Science, Mitchell Park Horticultural Conservatory, Gold Dome, Tacoma Dome, and Spaceship Earth (Disney).''
'Buckminsterfullerene' (IUPAC name '(C60-Ih)[5,6]fullerene') is the smallest fullerene molecule in which no two pentagons share an edge (which can be destabilizing; see pentalene). It is also the most common in terms of natural occurrence, as it can often be found in soot.
The structure of C60 is a truncated (T = 3) icosahedron, which resembles a soccer ball of the type made of hexagons and pentagons, with a carbon atom at the vertices of each polygon and a bond along each polygon edge.
The diameter of a C60 molecule is about 1 nanometer (nm).
The C60 molecule has two bond lengths. The 6:6 ring bonds (between two hexagons) can be considered "double bonds" and are shorter than the 6:5 bonds (between a hexagon and a pentagon).
'Nanotubes' are cylindrical fullerenes. These tubes of carbon are usually only a few nanometres wide, but they can range from less than a micrometre to several millimetres in length. They often have closed ends, but can be open-ended as well. There are also cases in which the tube reduces in diameter before closing off. Their unique molecular structure results in extraordinary macroscopic properties, including high tensile strength, high electrical conductivity, high ductility, high resistance to heat, and relative chemical inactivity (as it is cylindrical and 'planar' — that is, it has no 'exposed' atoms that can be easily displaced).
A new type of buckyball utilizing boron atoms instead of the usual carbon has been predicted and described by researchers at Rice University. The B-80 structure is predicted to be more stable than the C-60 buckyball. [1] One reason for this given by the researchers is that the B-80 is actually more like the original geodesic dome structure popularized by Buckminster Fuller which utilizes triangles rather than hexagons.
In mathematical terms, the structure of a 'fullerene' is a trivalent convex polyhedron with pentagonal and hexagonal faces. In graph theory, the term 'fullerene' refers to any 3-regular, planar graph with all faces of size 5 or 6 (including the external face). It follows from Euler's polyhedron formula, |V|-|E|+|F| = 2, (where |V|, |E|, |F| indicate the number of vertices, edges, and faces), that there are exactly 12 pentagons in a fullerene and |V|/2-10 hexagons.
The smallest fullerene is the dodecahedron--the unique C20, dodecahedrane. There are no fullerenes with 22 vertices. The number of fullerenes C2n grows with increasing n = 12,13,14..., roughly in proportion to n9. For instance, there are 1812 non-isomorphic fullerenes C60. Note that only one form of C60, the buckminsterfullerene alias truncated icosahedron, has no pair of adjacent pentagons (the smallest such fullerene). To further illustrate the growth, there are 214,127,713 non-isomorphic fullerenes C200, 15,655,672 of which have no adjacent pentagons.
For the past decade, the chemical and physical properties of fullerenes have been a hot topic in the field of research and development, and are likely to continue to be for a long time. Popular Science has published articles about the possible uses of fullerenes in armor. In April 2003, fullerenes were under study for potential medicinal use: binding specific antibiotics to the structure to target resistant bacteria and even target certain cancer cells such as melanoma. The October 2005 issue of Chemistry and Biology contains an article describing the use of fullerenes as light-activated antimicrobial agents.[2]
In the field of nanotechnology, heat resistance and superconductivity are some of the more heavily studied properties.
A common method used to produce fullerenes is to send a large current between two nearby graphite electrodes in an inert atmosphere. The resulting carbon plasma arc between the electrodes cools into sooty residue from which many fullerenes can be isolated.
There are many calculations that have been done using ab-initio Quantum Methods applied to fullerenes. By DFT and TDDFT methods one can obtain IR, Raman and UV spectra. Results of such calculations can be compared with experimental results.
Researchers have been able to increase the reactivity of fullerenes by attaching active groups to their surfaces. Buckminsterfullerene does not exhibit "superaromaticity": that is, the electrons in the hexagonal rings do not delocalize over the whole molecule.
A spherical fullerene of ''n'' carbon atoms has ''n'' pi-bonding electrons. These should try to delocalize over the whole molecule. The quantum mechanics of such an arrangement should be like one shell only of the well-known quantum mechanical structure of a single atom, with a stable filled shell for ''n'' = 2, 8, 18, 32, 50, 72, 98, 128, etc, i.e. twice a perfect square; but this series does not include 60. As a result, C60 in water tends to pick up two more electrons and become an anion. The nC60 described below may be the result of C60's trying to form a metallic bonding type loose combination.
Fullerenes are stable, but not totally nonreactive. The sp2-hybridized carbon atoms, which are at their energy minimum in planar graphite, must be bent to form the closed sphere or tube, which produces angle strain. The characteristic reaction of fullerenes is electrophilic addition at 6,6-double bonds, which reduces angle strain by changing sp2-hybridized carbons into sp3-hybridized ones.[1] The change in hybridized orbitals causes the bond angles to decrease from about 120 degrees in the sp2 orbitals to about 109.5 degrees in the sp3 orbitals. This decrease in bond angles allows for the bonds to bend less when closing the sphere or tube, and thus, the molecule becomes more stable.
Other atoms can be trapped inside fullerenes to form inclusion compounds known as endohedral fullerenes. An unusual example is the egg shaped fullerene Tb3N@C84, which violates the isolated pentagon rule [3] Recent evidence for a meteor impact at the end of the Permian period was found by analysing noble gases so preserved.[4] Metallofullerene-based inoculates using the rhonditic steel process are beginning production as one of the first commercially-viable uses of buckyballs.
Fullerenes are sparingly soluble in many solvents. Common solvents for the fullerenes include aromatics such as toluene and carbon disulfide. Solutions of pure Buckminsterfullerene have a deep purple color. Solutions of C70 are a reddish brown. The higher fullerenes C76 to C84 have a variety of colors. C76 has two optical forms, while other higher fullerenes have several structural isomers. Fullerenes are the only known allotrope of carbon that can be dissolved in common solvents at room temperature.
Some fullerene structures are not soluble because they have a small bandgap between the ground and excited states. These include the small fullerenes C36 and C50. The C72 structure is also in this class, but the endohedral version with a trapped lanthanide-group atom is soluble due to the interaction of the metal atom and the electronic states of the fullerene. Researchers had originally been puzzled by C72 being absent in fullerene plasma-generated soot extract, but found in endohedral samples. Small band gap fullerenes are highly reactive and bind to other fullerenes or to soot particles.
Solvents that are able to dissolve a fullerene extract mixture (C60 / C70) are listed below in order from highest solubility. The value in parentheses is the approximate saturated concentration.
# 1,2,4-trichlorobenzene (20 mg/ml)
# carbon disulfide (12 mg/ml)
# toluene (3.2 mg/ml)
# benzene (1.8 mg/ml)
# chloroform (0.5 mg/ml)
# carbon tetrachloride (0.4 mg/ml)
# cyclohexane (0.054 mg/ml)
# n-hexane (0.046 mg/ml)
# tetrahydrofuran (0.037 mg/ml)
# acetonitrile (0.02 mg/ml)
# methanol (0.0009 mg/ml)
In 1999, researchers from the University of Vienna demonstrated that the wave-particle duality applied to macro-molecules such as fullerene[5]. One of the co-authors of this research, Julian Voss-Andreae became an artist and has since created several sculptures symbolizing wave-particle duality in Buckminsterfullerenes.
Science writer Marcus Chown made a reference on the CBC radio show "Quirks And Quarks" in May 2006 that there is a scientist working on having buckyballs follow the quantum behavior of atoms of appearing to be in two places at once. The work is continuing on this phenomenon.[6].
Although fullerene C60 has been thought in theory to be relatively inert, a presentation given to the American Chemical Society in March 2004 and described in an article in New Scientist on April 3 2004, suggests the molecule is injurious to organisms. An experiment by Eva Oberdörster at Southern Methodist University, which introduced fullerenes into water at concentrations of 0.5 parts per million, found that largemouth bass suffered a 17-fold increase in cellular damage in the brain tissue after 48 hours.
Main articles: Fullerenes in popular culture
Examples of fullerenes in popular culture are numerous. In fact, fullerenes appeared in fiction well before science started to take serious interest in them.
★ It is the topic of a science fiction book named ''Decipher'' written by Stel Pavlou
★ In ''New Scientist'' there used to be a weekly column called ''Daedalus'' written by David Jones, which contained humorous descriptions of unlikely technologies. In 1966 the columnist included a description of the C60 and other forms of graphite. This was meant as pure entertainment.
★ Also in the ''New Scientist'' magazine, a free book was enclosed entitled, "100 Things to Do Before You Die", one of which was to kick a buckyball.
★ The buckyball is the state molecule of Texas [7]
★ Buckypaper
★ Carbon nanotube
★ NanoBud
★ Dodecahedrane
★ Endohedral fullerenes
★ Geodesic dome
★ Graphene
★ Polyhedron
★ Prismane C8
★ Carbon
★ Atomic carbon
★ Truncated rhombic triacontahedron
★ The Most Beautiful Molecule: The Discovery of the Buckyball, , Hugh, Aldersey-Williams, John Wiley & Sons, 1995, ISBN 0-471-19333-X
1. ''Bucky's brother -- The boron buckyball makes its debut'' Jade Boyd April '2007' eurekalert.orgLink
2. Cationic Fullerenes Are Effective and Selective Antimicrobial Photosensitizers, , G., Tegos, Chemistry & Biology, 2005
3. egg shaped fullerene: Link.
4.
5. Wave-particle duality of C60, , M., Arndt, Nature, 1999
6. The radio show can be heard at: http://www.cbc.ca/quirks/archives/05-06/jun17.html
7. State molecule of Texas: Link
★ Fullerene and nanotube Gallery
★ Properties of C60 fullerene
★ [2]
★ Buckyball Workshops by Sir Harry Kroto and the Vega Science Trust
★ Center for Nanoscale Science and Technology
★ Center for Biological and Environmental Nanotechnology
★ Dr. Smalley's brief autobiography
★ Dr. Smalley's webpage
★ Sir Harry Kroto's webpage
★ Interview with James R. Heath, discussing the discovery of C60
★ Carbon Fullerene & Nanotube Models Vincent Herr, Houston, TX
★ Diffraction and Interference with Fullerenes: Wave-particle duality of C60, University of Vienna
★ Fullerene-based architectures for quantum computing in Germany and in Great Britain at the QIP IRC
★ Molview from bluerhinos.co.uk See Buckminsterfullerene (C60) in 3D
★ Computational Chemistry Wiki
★ A Spherical Revelation
★ C60 3D-view and pdb-file
★ Simple model of Fullerene.
★ Story on "Buckyeggs" (UC Davis website)
★ Stainless Steel Buckminster Fullerenes
★ Rhonditic Steel
The Icosahedral Fullerene C540
''"C60", "C-60" and "Buckyballs" redirect here.''
The 'fullerenes', discovered in 1985 by researchers at the University of Sussex and Rice University, are a family of carbon allotropes named after Richard Buckminster Fuller and are sometimes called 'buckyballs'. They are molecules composed entirely of carbon, in the form of a hollow sphere, ellipsoid, or tube. Cylindrical fullerenes are called carbon nanotubes or 'buckytubes'. Fullerenes are similar in structure to graphite, which is composed of a sheet of linked hexagonal rings, but they contain also pentagonal (or sometimes heptagonal) rings that prevent the sheet from being planar.
Prediction and discovery
In molecular beam experiments, discrete peaks were observed corresponding to molecules with the exact mass of sixty or seventy or more carbon atoms. In 1985, Harold Kroto (then of the University of Sussex, now of Florida State University), James R. Heath, Sean O'Brien, Robert Curl and Richard Smalley, from Rice University, discovered C60, and shortly thereafter came to discover the fullerenes. Kroto, Curl, and Smalley were awarded the 1996 Nobel Prize in Chemistry for their roles in the discovery of this class of compounds. C60 and other fullerenes were later noticed occurring outside the laboratory (e.g., in normal candle soot). By 1991, it was relatively easy to produce gram-sized samples of fullerene powder using the techniques of Donald Huffman and Wolfgang Krätschmer. Fullerene purification remains a challenge to chemists and to a large extent determines fullerene prices. So-called endohedral fullerenes have ions or small molecules incorporated inside the cage atoms. Fullerene is an unusual reactant in many organic reactions such as the Bingel reaction discovered in 1993.
The existence of C60 was predicted in 1970 by Eiji Osawa of Toyohashi University of Technology. He noticed that the structure of a corannulene molecule was a subset of a soccer-ball shape, and he made the hypothesis that a full ball shape could also exist. His idea was reported in Japanese magazines, but did not reach Europe or America.
Naming
Buckminsterfullerene (C60) was named after Richard Buckminster Fuller, a noted architect who popularized the geodesic dome. Since buckminsterfullerenes have a similar shape to that sort of dome, the name was thought to be appropriate. As the discovery of the fullerene family came ''after'' buckminsterfullerene, the name was shortened to illustrate that the latter is a type of the former.
''For illustrations of geodesic dome structures, see Montreal Biosphere, Eden Project, Missouri Botanical Gardens, Science World at TELUS World of Science, Mitchell Park Horticultural Conservatory, Gold Dome, Tacoma Dome, and Spaceship Earth (Disney).''
Types of fullerenes
Buckminsterfullerene C60
Buckminsterfullerene
'Buckminsterfullerene' (IUPAC name '(C60-Ih)[5,6]fullerene') is the smallest fullerene molecule in which no two pentagons share an edge (which can be destabilizing; see pentalene). It is also the most common in terms of natural occurrence, as it can often be found in soot.
The structure of C60 is a truncated (T = 3) icosahedron, which resembles a soccer ball of the type made of hexagons and pentagons, with a carbon atom at the vertices of each polygon and a bond along each polygon edge.
The diameter of a C60 molecule is about 1 nanometer (nm).
The C60 molecule has two bond lengths. The 6:6 ring bonds (between two hexagons) can be considered "double bonds" and are shorter than the 6:5 bonds (between a hexagon and a pentagon).
Carbon nanotubes
This animation of a rotating Carbon nanotube shows its 3D structure.
'Nanotubes' are cylindrical fullerenes. These tubes of carbon are usually only a few nanometres wide, but they can range from less than a micrometre to several millimetres in length. They often have closed ends, but can be open-ended as well. There are also cases in which the tube reduces in diameter before closing off. Their unique molecular structure results in extraordinary macroscopic properties, including high tensile strength, high electrical conductivity, high ductility, high resistance to heat, and relative chemical inactivity (as it is cylindrical and 'planar' — that is, it has no 'exposed' atoms that can be easily displaced).
Boron buckyball
A new type of buckyball utilizing boron atoms instead of the usual carbon has been predicted and described by researchers at Rice University. The B-80 structure is predicted to be more stable than the C-60 buckyball. [1] One reason for this given by the researchers is that the B-80 is actually more like the original geodesic dome structure popularized by Buckminster Fuller which utilizes triangles rather than hexagons.
Mathematics behind fullerenes
In mathematical terms, the structure of a 'fullerene' is a trivalent convex polyhedron with pentagonal and hexagonal faces. In graph theory, the term 'fullerene' refers to any 3-regular, planar graph with all faces of size 5 or 6 (including the external face). It follows from Euler's polyhedron formula, |V|-|E|+|F| = 2, (where |V|, |E|, |F| indicate the number of vertices, edges, and faces), that there are exactly 12 pentagons in a fullerene and |V|/2-10 hexagons.
The smallest fullerene is the dodecahedron--the unique C20, dodecahedrane. There are no fullerenes with 22 vertices. The number of fullerenes C2n grows with increasing n = 12,13,14..., roughly in proportion to n9. For instance, there are 1812 non-isomorphic fullerenes C60. Note that only one form of C60, the buckminsterfullerene alias truncated icosahedron, has no pair of adjacent pentagons (the smallest such fullerene). To further illustrate the growth, there are 214,127,713 non-isomorphic fullerenes C200, 15,655,672 of which have no adjacent pentagons.
Properties
For the past decade, the chemical and physical properties of fullerenes have been a hot topic in the field of research and development, and are likely to continue to be for a long time. Popular Science has published articles about the possible uses of fullerenes in armor. In April 2003, fullerenes were under study for potential medicinal use: binding specific antibiotics to the structure to target resistant bacteria and even target certain cancer cells such as melanoma. The October 2005 issue of Chemistry and Biology contains an article describing the use of fullerenes as light-activated antimicrobial agents.[2]
In the field of nanotechnology, heat resistance and superconductivity are some of the more heavily studied properties.
A common method used to produce fullerenes is to send a large current between two nearby graphite electrodes in an inert atmosphere. The resulting carbon plasma arc between the electrodes cools into sooty residue from which many fullerenes can be isolated.
There are many calculations that have been done using ab-initio Quantum Methods applied to fullerenes. By DFT and TDDFT methods one can obtain IR, Raman and UV spectra. Results of such calculations can be compared with experimental results.
Aromaticity
Researchers have been able to increase the reactivity of fullerenes by attaching active groups to their surfaces. Buckminsterfullerene does not exhibit "superaromaticity": that is, the electrons in the hexagonal rings do not delocalize over the whole molecule.
A spherical fullerene of ''n'' carbon atoms has ''n'' pi-bonding electrons. These should try to delocalize over the whole molecule. The quantum mechanics of such an arrangement should be like one shell only of the well-known quantum mechanical structure of a single atom, with a stable filled shell for ''n'' = 2, 8, 18, 32, 50, 72, 98, 128, etc, i.e. twice a perfect square; but this series does not include 60. As a result, C60 in water tends to pick up two more electrons and become an anion. The nC60 described below may be the result of C60's trying to form a metallic bonding type loose combination.
Chemistry
Fullerenes are stable, but not totally nonreactive. The sp2-hybridized carbon atoms, which are at their energy minimum in planar graphite, must be bent to form the closed sphere or tube, which produces angle strain. The characteristic reaction of fullerenes is electrophilic addition at 6,6-double bonds, which reduces angle strain by changing sp2-hybridized carbons into sp3-hybridized ones.[1] The change in hybridized orbitals causes the bond angles to decrease from about 120 degrees in the sp2 orbitals to about 109.5 degrees in the sp3 orbitals. This decrease in bond angles allows for the bonds to bend less when closing the sphere or tube, and thus, the molecule becomes more stable.
Other atoms can be trapped inside fullerenes to form inclusion compounds known as endohedral fullerenes. An unusual example is the egg shaped fullerene Tb3N@C84, which violates the isolated pentagon rule [3] Recent evidence for a meteor impact at the end of the Permian period was found by analysing noble gases so preserved.[4] Metallofullerene-based inoculates using the rhonditic steel process are beginning production as one of the first commercially-viable uses of buckyballs.
Solubility
The ''C''60 fullerene in crystalline form
Fullerenes are sparingly soluble in many solvents. Common solvents for the fullerenes include aromatics such as toluene and carbon disulfide. Solutions of pure Buckminsterfullerene have a deep purple color. Solutions of C70 are a reddish brown. The higher fullerenes C76 to C84 have a variety of colors. C76 has two optical forms, while other higher fullerenes have several structural isomers. Fullerenes are the only known allotrope of carbon that can be dissolved in common solvents at room temperature.
Some fullerene structures are not soluble because they have a small bandgap between the ground and excited states. These include the small fullerenes C36 and C50. The C72 structure is also in this class, but the endohedral version with a trapped lanthanide-group atom is soluble due to the interaction of the metal atom and the electronic states of the fullerene. Researchers had originally been puzzled by C72 being absent in fullerene plasma-generated soot extract, but found in endohedral samples. Small band gap fullerenes are highly reactive and bind to other fullerenes or to soot particles.
Solvents that are able to dissolve a fullerene extract mixture (C60 / C70) are listed below in order from highest solubility. The value in parentheses is the approximate saturated concentration.
# 1,2,4-trichlorobenzene (20 mg/ml)
# carbon disulfide (12 mg/ml)
# toluene (3.2 mg/ml)
# benzene (1.8 mg/ml)
# chloroform (0.5 mg/ml)
# carbon tetrachloride (0.4 mg/ml)
# cyclohexane (0.054 mg/ml)
# n-hexane (0.046 mg/ml)
# tetrahydrofuran (0.037 mg/ml)
# acetonitrile (0.02 mg/ml)
# methanol (0.0009 mg/ml)
Quantum mechanics
In 1999, researchers from the University of Vienna demonstrated that the wave-particle duality applied to macro-molecules such as fullerene[5]. One of the co-authors of this research, Julian Voss-Andreae became an artist and has since created several sculptures symbolizing wave-particle duality in Buckminsterfullerenes.
Science writer Marcus Chown made a reference on the CBC radio show "Quirks And Quarks" in May 2006 that there is a scientist working on having buckyballs follow the quantum behavior of atoms of appearing to be in two places at once. The work is continuing on this phenomenon.[6].
Safety issues
Although fullerene C60 has been thought in theory to be relatively inert, a presentation given to the American Chemical Society in March 2004 and described in an article in New Scientist on April 3 2004, suggests the molecule is injurious to organisms. An experiment by Eva Oberdörster at Southern Methodist University, which introduced fullerenes into water at concentrations of 0.5 parts per million, found that largemouth bass suffered a 17-fold increase in cellular damage in the brain tissue after 48 hours.
Popular culture
Main articles: Fullerenes in popular culture
Examples of fullerenes in popular culture are numerous. In fact, fullerenes appeared in fiction well before science started to take serious interest in them.
★ It is the topic of a science fiction book named ''Decipher'' written by Stel Pavlou
★ In ''New Scientist'' there used to be a weekly column called ''Daedalus'' written by David Jones, which contained humorous descriptions of unlikely technologies. In 1966 the columnist included a description of the C60 and other forms of graphite. This was meant as pure entertainment.
★ Also in the ''New Scientist'' magazine, a free book was enclosed entitled, "100 Things to Do Before You Die", one of which was to kick a buckyball.
★ The buckyball is the state molecule of Texas [7]
See also
★ Buckypaper
★ Carbon nanotube
★ NanoBud
★ Dodecahedrane
★ Endohedral fullerenes
★ Geodesic dome
★ Graphene
★ Polyhedron
★ Prismane C8
★ Carbon
★ Atomic carbon
★ Truncated rhombic triacontahedron
Further reading
★ The Most Beautiful Molecule: The Discovery of the Buckyball, , Hugh, Aldersey-Williams, John Wiley & Sons, 1995, ISBN 0-471-19333-X
References
1. ''Bucky's brother -- The boron buckyball makes its debut'' Jade Boyd April '2007' eurekalert.orgLink
2. Cationic Fullerenes Are Effective and Selective Antimicrobial Photosensitizers, , G., Tegos, Chemistry & Biology, 2005
3. egg shaped fullerene: Link.
4.
5. Wave-particle duality of C60, , M., Arndt, Nature, 1999
6. The radio show can be heard at: http://www.cbc.ca/quirks/archives/05-06/jun17.html
7. State molecule of Texas: Link
External links
★ Fullerene and nanotube Gallery
★ Properties of C60 fullerene
★ [2]
★ Buckyball Workshops by Sir Harry Kroto and the Vega Science Trust
★ Center for Nanoscale Science and Technology
★ Center for Biological and Environmental Nanotechnology
★ Dr. Smalley's brief autobiography
★ Dr. Smalley's webpage
★ Sir Harry Kroto's webpage
★ Interview with James R. Heath, discussing the discovery of C60
★ Carbon Fullerene & Nanotube Models Vincent Herr, Houston, TX
★ Diffraction and Interference with Fullerenes: Wave-particle duality of C60, University of Vienna
★ Fullerene-based architectures for quantum computing in Germany and in Great Britain at the QIP IRC
★ Molview from bluerhinos.co.uk See Buckminsterfullerene (C60) in 3D
★ Computational Chemistry Wiki
★ A Spherical Revelation
★ C60 3D-view and pdb-file
★ Simple model of Fullerene.
★ Story on "Buckyeggs" (UC Davis website)
★ Stainless Steel Buckminster Fullerenes
★ Rhonditic Steel
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