Endohedral fullerene

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Rendering of a buckminsterfullerene containing an atom (M@C60).

Endohedral fullerenes, also called endofullerenes, are fullerenes that have additional atoms, ions, or clusters enclosed within their inner spheres. The first lanthanum C60 complex was synthesized in 1985 called La@C60. The @ (at sign) in the name reflects the notion of a small molecule trapped inside a shell. Two types of endohedral complexes exist: endohedral metallofullerenes and non-metal doped fullerenes.[1]

Notation[edit]

In a traditional chemical formula notation, a buckminsterfullerene (C60) with an atom (M) was simply represented as MC60 regardless of whether M was inside or outside the fullerene. In order to allow for more detailed discussions with minimal loss of information, a more explicit notation was proposed in 1991,[2] where the atoms listed to the left of the @ sign is situated inside the network composed of the atoms listed to the right. The example above would then be denoted M@C60 if M were inside the carbon network. A more complex example is K2(K@C59B), which denotes "a 60-atom fullerene cage with one boron atom substituted for a carbon in the geodesic network, a single potassium trapped inside, and two potassium atoms adhering to the outside."[2]

The choice of the symbol has been explained by the authors as being concise, readily printed and transmitted electronically (the at sign is included in ASCII, which most modern character encoding schemes are based on), and the visual aspects suggesting the structure of an endohedral fullerene.

Endohedral metallofullerenes[edit]

Doping fullerenes with electropositive metals takes place in an arc reactor or via laser evaporation. The metals can be transition metals like scandium, yttrium as well as lanthanides like lanthanum and cerium. Also possible are endohedral complexes with elements of the alkaline earth metals like barium and strontium, alkali metals like potassium and tetravalent metals like uranium, zirconium and hafnium. The synthesis in the arc reactor is however unspecific. Besides unfilled fullerenes, endohedral metallofullerenes develop with different cage sizes like La@C60 or La@C82 and as different isomer cages. Aside from the dominant presence of mono-metal cages, numerous di-metal endohedral complexes and the tri-metal carbide fullerenes like Sc3C2@C80 were also isolated.

In 1998 a discovery drew large attention. With the synthesis of the Sc3N@C80, the inclusion of a molecule fragment in a fullerene cage had succeeded for the first time. This compound can be prepared by arc-vaporization at temperatures up to 1100 °C of graphite rods packed with scandium(III) oxide iron nitride and graphite powder in a K-H generator in a nitrogen atmosphere at 300 Torr.[3]

Endohedral metallofullerenes are characterised by the fact that electrons will transfer from the metal atom to the fullerene cage and that the metal atom takes a position off-center in the cage. The size of the charge transfer is not always simple to determine. In most cases it is between 2 and 3 charge units, in the case of the La2@C80 however it can be even about 6 electrons such as in Sc3N@C80 which is better described as [Sc3N]+6@[C80]−6. These anionic fullerene cages are very stable molecules and do not have the reactivity associated with ordinary empty fullerenes. They are stable in air up to very high temperatures (600 to 850°C).

The lack of reactivity in Diels-Alder reactions is utilised in a method to purify [C80]−6 compounds from a complex mixture of empty and partly filled fullerenes of different cage size.[3] In this method Merrifield resin is modified as a cyclopentadienyl resin and used as a solid phase against a mobile phase containing the complex mixture in a column chromatography operation. Only very stable fullerenes such as [Sc3N]+6@[C80]−6 pass through the column unreacted.

In Ce2@C80 the two metal atoms exhibit a non-bonded interaction.[4] Since all the six-membered rings in C80-Ih are equal[4] the two encapsulated Ce atoms exhibit a three-dimensional random motion.[5] This is evidenced by the presence of only two signals in the 13C-NMR spectrum. It is possible to force the metal atoms to a standstill at the equator as shown by x-ray crystallography when the fullerene is exahedrally functionalized by an electron donation silyl group in a reaction of Ce2@C80 with 1,1,2,2-tetrakis(2,4,6-trimethylphenyl)-1,2-disilirane.

Non-metal doped fullerenes[edit]

Saunders in 1993 showed the formation of endohedral complexes He@C60 and Ne@C60 when C60 is exposed to a pressure of around 3 bar of the noble gases.[6] Under these conditions about one out of every 650,000 C60 cages was doped with a helium atom. The formation of endohedral complexes with helium, neon, argon, krypton and xenon as well as numerous adducts of the He@C60 compound was also demonstrated[7] with pressures of 3 kbars and incorporation of up to 0.1% of the noble gases.

While noble gases are chemically very inert and commonly exist as individual atoms, this is not the case for nitrogen and phosphorus and so the formation of the endohedral complexes N@C60, N@C70 and P@C60 is more surprising. The nitrogen atom is in its electronic initial state (4S3/2) and is therefore to be highly reactive. Nevertheless N@C60 is sufficiently stable that exohedral derivatization from the mono- to the hexa adduct of the malonic acid ethyl ester is possible. In these compounds no charge transfer[disambiguation needed] of the nitrogen atom in the center to the carbon atoms of the cage takes place. Therefore 13C-couplings, which are observed very easily with the endohedral metallofullerenes, could only be observed in the case of the N@C60 in a high resolution spectrum as shoulders of the central line.

The central atom in these endohedral complexes is located in the center of the cage. While other atomic traps require complex equipment, e.g. laser cooling or magnetic traps, endohedral fullerenes represent an atomic trap that is stable at room temperature and for an arbitrarily long time. Atomic or ion traps are of great interest since particles are present free from (significant) interaction with their environment, allowing unique quantum mechanical phenomena to be explored. For example, the compression of the atomic wave function as a consequence of the packing in the cage could be observed with ENDOR spectroscopy. The nitrogen atom can be used as a probe, in order to detect the smallest changes of the electronic structure of its environment.

Contrary to the metallo endohedral compounds, these complexes cannot be produced in an arc. Atoms are implanted in the fullerene starting material using gas discharge (nitrogen and phosphorus complexes) or by direct ion implantation. Alternatively, endohedral hydrogen fullerenes can be produced by opening and closing a fullerene by organic chemistry methods. A recent example of endohedral fullerenes includes single molecules of water encapsulated in C60.[8] Water endofullerene is a young compound and has been poorly studied. The most interesting in such endofullerenes is their hypothetical ability to transform into endohedral covalent derivatives, a new class of fullerene derivatives. One of the examples of the mentioned interconversions, induced by compression, has been studied by DFT methods.[9]

According to state-of-the-art DFT calculations, noble gas endofullerenes should demonstrate unusual polarizability. Thus, calculated values of mean polarizability of Ng@C60 do not equal to the sum of polarizabilities of a fullerene cage and the trapped atom, i.e. exaltation of polarizability occurs.,.[10][11] As shown in [10], the sign of the Δα polarizability exaltation depends on the number of atoms in a fullerene molecule: for small fullerenes (n<30), it is positive; for the larger ones (n>30), it is negative (depression of polarizability). Sabirov has proposed the following formula, describing the dependence of Δα on n: Δα = αNg(2e–0.06(n – 20)-1) [10]. It describes the DFT-calculated mean polarizabilities of Ng@C60 endofullerenes with sufficient accuracy. The calculated data allows using C60 fullerene as a Faraday cage,[12] which isolates the encapsulated atom from the external electric field. The mentioned relations should be typical for the more complicated endohedral structures (e.g., C60@C240[13] and giant fullerene-containing onions [14]).

Molecular endofullerenes[edit]

Closed fullerenes encapsulating small molecules have been synthesized by long sequences of organic reactions. Notable achievements are the synthesis of the dihydrogen endofullerene H2@C60 and the water endofullerene H2O@C60 by the groups of Komatsu [15] and Murata.[16] The encapsulated molecules display unusual physical properties which have been studied by a variety of physical methods.[17]

See also[edit]

References[edit]

  1. ^ Periodic table of endohedral fullerene atoms[Broken Link]
  2. ^ a b Chai, Yan; Guo, Ting; Jin, Changming; Haufler, Robert E.; Chibante, L. P. Felipe; Fure, Jan; Wang, Lihong; Alford, J. Michael; Smalley, Richard E. (1991). "Fullerenes wlth Metals Inside". Journal of Physical Chemistry 95 (20): 7564–7568. doi:10.1021/j100173a002. 
  3. ^ a b Ge, Z; Duchamp, Jc; Cai, T; Gibson, Hw; Dorn, Hc (2005). "Purification of endohedral trimetallic nitride fullerenes in a single, facile step". Journal of the American Chemical Society 127 (46): 16292–8. doi:10.1021/ja055089t. PMID 16287323. 
  4. ^ a b K.Muthukumar; J.A.Larsson (2008). "Explanation of the different preferential binding sites for Ce and La in M2@C80 (M = Ce, La". Journal of Materials Chemistry 18 (28): 3347–51. doi:10.1039/b804168g. 
  5. ^ Yamada, M; Nakahodo, T; Wakahara, T; Tsuchiya, T; Maeda, Y; Akasaka, T; Kako, M; Yoza, K; Horn, E; Mizorogi, N; Kobayashi, K; Nagase, S (2005). "Positional control of encapsulated atoms inside a fullerene cage by exohedral addition". Journal of the American Chemical Society 127 (42): 14570–1. doi:10.1021/ja054346r. PMID 16231899. 
  6. ^ M. Saunders, H. A. Jiménez-Vázquez, R. J. Cross, and R. J. Poreda (1993). "Stable compounds of helium and neon. He@C60 and Ne@C60". Science 259 (5100): 1428–1430. Bibcode:1993Sci...259.1428S. doi:10.1126/science.259.5100.1428. PMID 17801275. 
  7. ^ Martin Saunders, Hugo A. Jimenez-Vazquez, R. James Cross, Stanley Mroczkowski, Michael L. Gross, Daryl E. Giblin, and Robert J. Poreda (1994). "Incorporation of helium, neon, argon, krypton, and xenon into fullerenes using high pressure". J. Am. Chem. Soc. 116 (5): 2193–2194. doi:10.1021/ja00084a089. 
  8. ^ A Single Molecule of Water Encapsulated in Fullerene C60 Kei Kurotobi and Yasujiro Murata. Science, 2012, 333, 613. doi:10.1126/science.1206376
  9. ^ From Endohedral Complexes to Endohedral Fullerene Covalent Derivatives: A DFT-Prognosis of Chemical Transformation of Water Endofullerene H2O@C60 upon its Compression. Denis Sabirov. J. Phys. Chem. C, 2012, doi:10.1021/jp310673j
  10. ^ Polarizability exaltation of endofullerenes X@Cn (n = 20, 24, 28, 36, 50, and 60; X is a noble gas atom) D. Sabirov & R. Bulgakov, JETP Lett., 2010, 92, 662. doi:10.1134/S0021364010220054
  11. ^ Dipole polarizabilities of noble gas endohedral fullerenes Hong Yan et al. Chem. Phys. Lett, 2008, 456, 223. doi:10.1016/j.cplett.2008.03.046
  12. ^ C60 as a Faraday cage P. Delaney & J. C. Greer, Appl. Phys. Lett., 2004, 84, 431. doi:10.1063/1.1640783
  13. ^ Electronic structure and static dipole polarizability of C60@C240 R. R. Zope, J. Phys. B: At. Mol. Opt. Phys., 2008, 41, 085101. doi:10.1088/0953-4075/41/8/085101
  14. ^ Study of the polarizability of fullerenes with a monopole–dipole interaction model R. Langlet et al., Diamond Relat. Mater., 2007, 16, 2145. doi:10.1016/j.diamond.2007.10.019
  15. ^ K. Komatsu, M. Murata and Y. Murata, Science 307, 238-240 (2005)
  16. ^ K. Kurotobi and Y. Murata, Science 333, 613-616 (2011)
  17. ^ M. H. Levitt, Phil. Trans. R. Soc. A 371, 20120429 (2013)

External links[edit]