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Fullerene chemistry

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Fullerene C60
Fullerene C60

Fullerene chemistry is a field of organic chemistry devoted to the chemical properties of fullerenes.[1][2][3] Research in this field is driven by the need to functionalize fullerenes and tune their properties. For example, fullerene is notoriously insoluble and adding a suitable group can enhance solubility.[1] By adding a polymerizable group, a fullerene polymer can be obtained. Functionalized fullerenes are divided into two classes: exohedral fullerenes with substituents outside the cage and endohedral fullerenes with trapped molecules inside the cage.

This article covers the chemistry of these so-called "buckyballs," while the chemistry of carbon nanotubes is covered in carbon nanotube chemistry.

Chemical properties of fullerenes

[edit]
See also: Endohedral fullerenes

Fullerene or C60 is soccer-ball-shaped or Ih with 12 pentagons and 20 hexagons. According to Euler's theorem these 12 pentagons are required for closure of the carbon network consisting of n hexagons and C60 is the first stable fullerene because it is the smallest possible to obey this rule. In this structure none of the pentagons make contact with each other. Both C60 and its relative C70 obey this so-called isolated pentagon rule (IPR). The next homologue C84 has 24 IPR isomers of which several are isolated and another 51,568 non-IPR isomers. Non-IPR fullerenes have thus far only been isolated as endohedral fullerenes such as Tb3N@C84 with two fused pentagons at the apex of an egg-shaped cage.[4] or as fullerenes with exohedral stabilization such as C50Cl10 [5] and reportedly C60H8.[6] Fullerenes with fewer than 60 carbons do not obey isolated pentagon rule (IPR).

Because of the molecule's spherical shape the carbon atoms are highly pyramidalized, which has far-reaching consequences for reactivity. It is estimated that strain energy constitutes 80% of the heat of formation. The conjugated carbon atoms respond to deviation from planarity by orbital rehybridization of the sp² orbitals and π orbitals to a sp2.27 orbital with a gain in p-character. The p lobes extend further outside the surface than they do into the interior of the sphere and this is one of the reasons a fullerene is electronegative. The other reason is that the empty low-lying π* orbitals also have a high s character.

The double bonds in fullerene are not all the same. Two groups can be identified: 30 so-called [6,6] double bonds connect two hexagons and 60 [5,6] bonds connect a hexagon and a pentagon. Of the two the [6,6] bonds are shorter with more double-bond character and therefore a hexagon is often represented as a cyclohexatriene and a pentagon as a pentalene or [5]radialene. In other words, although the carbon atoms in fullerene are all conjugated the superstructure is not a super aromatic compound. The X-ray diffraction bond length values are 139.1 pm for the [6,6] bond and 145.5 pm for the [5,6] bond.

C60 fullerene has 60 π electrons but a closed shell configuration requires 72 electrons. The fullerene is able to acquire the missing electrons by reaction with potassium to form first the K
6C6−
60 salt and then the K
12C12−
60 In this compound the bond length alternation observed in the parent molecule has vanished.

Fullerene reactions

[edit]
See also: Bingel reaction and Prato reaction

Fullerenes tend to react as electrophiles. An additional driving force is relief of strain when double bonds become saturated. Key in this type of reaction is the level of functionalization i.e. monoaddition or multiple additions and in case of multiple additions their topological relationships (new substituents huddled together or evenly spaced). In conformity with IUPAC rules, the terms methanofullerene are used to indicate the ring-closed (cyclopropane) fullerene derivatives, and fulleroid to ring-open (methanoannulene) structures.[7][8]

Nucleophilic additions

[edit]

Fullerenes react as electrophiles with a host of nucleophiles in nucleophilic additions. The intermediary formed carbanion is captured by another electrophile. Examples of nucleophiles are Grignard reagents and organolithium reagents. For example, the reaction of C60 with methylmagnesium chloride stops quantitatively at the penta-adduct with the methyl groups centered around a cyclopentadienyl anion which is subsequently protonated.[9] Another nucleophilic reaction is the Bingel reaction. Fullerene reacts with chlorobenzene and aluminium chloride in a Friedel-Crafts alkylation type reaction. In this hydroarylation the reaction product is the 1,2-addition adduct (Ar-CC-H).[10]

Pericyclic reactions

[edit]

The [6,6] bonds of fullerenes react as dienes or dienophiles in cycloadditions for instance Diels-Alder reactions. 4-membered rings can be obtained by [2+2]cycloadditions for instance with benzyne.[11][12] An example of a 1,3-dipolar cycloaddition to a 5-membered ring is the Prato reaction.

Hydrogenations

[edit]

Fullerenes are easily hydrogenated by several methods. The smallest perhydrogenated fullerene known is dodecahedrane C20H20, formally derived from the smallest possible but unknown fullerene, C20, which comprises just 12 pentagonal faces.

Examples of hydrofullerenes are C60H18 and C60H36. However, completely hydrogenated C60H60 is only hypothetical because of large strain. Highly hydrogenated fullerenes are not stable, as prolonged hydrogenation of fullerenes by direct reaction with hydrogen gas at high temperature conditions results in cage fragmentation. At the final reaction stage this causes collapse of cage structure with formation of polycyclic aromatic hydrocarbons.[13]

C60 reacts with Li[BHEt3] to the weak base [HC60]−, which is isolated as Li[HC60][H2O]6-9.[14]

Halogenation

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Fullerenes can react with halogens. The preferred pattern for addition C60 is calculated to be 1,9- for small groups and 1,7- for bulky groups. C60F60 is a possible structure. C60 reacts with Cl2 gas at 250 °C to a material with average composition C60Cl24, although only C60 can be detected by mass spectrometry.[14] With liquid Br2 C60 yields C60Br24, in which all 24 bromine atoms are equivalent. The only characterized iodine-containing compounds are intermediates: [C60][CH2I2][C6H6] and [C60][I2]2.[14]

Hydroxylations

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Fullerenes can be hydroxylated to fullerenols or fullerols. Water solubility depends on the total number of hydroxyl groups that can be attached. One method is fullerene reaction in diluted sulfuric acid and potassium nitrate to C60(OH)15.[15][16] Another method is reaction in diluted sodium hydroxide catalysed by TBAH adding 24 to 26 hydroxyl groups.[17] Hydroxylation has also been reported using solvent-free NaOH / hydrogen peroxide.[18] C60(OH)8 was prepared using a multistep procedure starting from a mixed peroxide fullerene.[19] The maximum number of hydroxyl groups that can be attached (hydrogen peroxide method) stands at 36–40.[20]

Electrophilic additions

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Fullerenes react in electrophilic additions as well. The reaction with bromine can add up to 24 bromine atoms to the sphere. The record holder for fluorine addition is C60F48. According to in silico predictions the as yet elusive C60F60 may have some of the fluorine atoms in endo positions (pointing inwards) and may resemble a tube more than it does a sphere.[21]

Eliminations

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Protocols have been investigated for removing substituents via eliminations after they have served their purpose. Examples are the retro-Bingel reaction and the retro-Prato reaction.

Carbene additions

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Fullerenes react with carbenes to methanofullerenes.[22] The reaction of fullerene with dichlorocarbene (created by sodium trichloroacetate pyrolysis) was first reported in 1993.[23] A single addition takes place along a [6,6] bond.

Radical additions

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Fullerenes can be considered radical scavengers.[24][25] With a simple hydrocarbon radical such as the t-butyl radical obtained by thermolysis or photolysis from a suitable precursor the tBuC60 radical is formed that can be studied. The unpaired electron does not delocalize over the entire sphere but takes up positions in the vicinity of the tBu substituent.

Fullerenes as ligands

[edit]
Main article: Fullerene ligands

Fullerene is a ligand in organometallic chemistry. The organometallic chemistry of C60 is dictated by its spherical geometry and localized polyalkene π-electronic structure. All reported derivatives are η2 complexe in which the metal coordinates at a six–six ring fusion with formal double bond. No analogous η4-diene or η6-triene complexes are prepared.[14]

C60 and C70 form complexes with a variety of molecules. In the solid state lattice structures are stabilized by the intermolecular interactions.[14] Charge transfer complexes are formed with weak electron donors. The [6,6] double bond is electron-deficient and usually forms metallic bonds with η = 2 hapticity. Bonding modes such as η = 5 or η = 6 can be induced by modification of the coordination sphere.

  • [C60][ferrocene]2, in which the C60 molecules are arranged in close-packed layers
  • [C60][1,4-dihydroquinone]3 has C60 molecules trapped in a hydrogen-bonded of 1,4-dihydroquinone molecules
  • The solvated C60 compounds: [C60][C6H6]4 and [C60][CH2I2][C6H6], and the intercalate [C60][I2]2, are structurally characterized.[14]
  • [C70][S8]6
  • [C60][γ-cyclodextrin]2
  • C60 fullerene reacts with tungsten hexacarbonyl W(CO)6 to the (η²-C60)W(CO)5 complex in a hexane solution in direct sunlight.[26]

Variants

[edit]

Open-cage fullerenes

[edit]

A part of fullerene research is devoted to so-called open-cage fullerenes [27] whereby one or more bonds are removed chemically exposing an orifice.[28] In this way it is possible to insert into it small molecules such as hydrogen, helium or lithium. The first such open-cage fullerene was reported in 1995.[29] In endohedral hydrogen fullerenes the opening, hydrogen insertion and closing back up has already been demonstrated.

Heterofullerenes

[edit]
Main article: heterofullerene

In heterofullerenes at least one carbon atom is replaced by another element.[30][31] Based on spectroscopy, substitutions have been reported with boron (borafullerenes),[32][33] nitrogen (azafullerenes),[34][35] oxygen,[36] arsenic, germanium,[37] phosphorus,[38] silicon,[39][40] iron, copper, nickel, rhodium[40][41] and iridium.[40] Reports on isolated heterofullerenes are limited to those based on nitrogen [42][43][44][45] and oxygen.[46]

The fullerene oxides C60O and C70O are observed in minor in fullerene-containing soot. Only C60O is isolated as a pure compound in macroscopic amounts.[14]

Fullerene dimers

[edit]

The C60 fullerene dimerizes in a formal [2+2] cycloaddition to a C120 bucky dumbbell in the solid state by mechanochemistry (high-speed vibration milling) with potassium cyanide as a catalyst.[47] The trimer has also been reported using 4-aminopyridine as catalyst (4% yield) [48] and observed with scanning tunneling microscopy as a monolayer.[49]

Synthesis

[edit]
See also: Buckminsterfullerene § Synthesis

Multistep fullerene synthesis

[edit]

Although the procedure for the synthesis of the C60 fullerene is well established (generation of a large current between two nearby graphite electrodes in an inert atmosphere) a 2002 study described an organic synthesis of the compound starting from simple organic compounds.[50][51]

Multistep fullerene synthesis

In the final step a large polycyclic aromatic hydrocarbon consisting of 13 hexagons and three pentagons was submitted to flash vacuum pyrolysis at 1100 °C and 0.01 Torr. The three carbon chlorine bonds served as free radical incubators and the ball was stitched up in a no-doubt complex series of radical reactions. The chemical yield was low: 0.1 to 1%. A small percentage of fullerenes is formed in any process which involves burning of hydrocarbons, e.g. in candle burning. The yield through a combustion method is often above 1%. The method proposed above does not provide any advantage for synthesis of fullerenes compared to the usual combustion method, and therefore, the organic synthesis of fullerenes remains a challenge for chemistry.

Continuous high-resolution transmission electron microscopic video imaging of the electron-beam-induced bottom-up synthesis of fullerene C60 through cyclodehydrogenation of C60H30 was reported in 2021.[52]

A similar exercise aimed at construction of a C78 cage in 2008 (but leaving out the precursor's halogens) did not result in a sufficient yield but at least the introduction of Stone Wales defects could be ruled out.[53] C60 synthesis through a fluorinated fullerene precursor was reported in 2013 [54]

Purification

[edit]

Fullerene purification is the process of obtaining a fullerene compound free of contamination. In fullerene production mixtures of C60, C70 and higher homologues are always formed. Fullerene purification is key to fullerene science and determines fullerene prices and the success of practical applications of fullerenes. The first available purification method for C60 fullerene was by HPLC from which small amounts could be generated at large expense.

A practical laboratory-scale method for purification of soot enriched in C60 and C70 starts with extraction in toluene followed by filtration with a paper filter. The solvent is evaporated and the residue (the toluene-soluble soot fraction) redissolved in toluene and subjected to column chromatography. C60 elutes first with a purple color and C70 is next displaying a reddish-brown color.[55]

In nanotube processing the established purification method for removing amorphous carbon and metals is by competitive oxidation (often a sulfuric acid / nitric acid mixture). It is assumed that this oxidation creates oxygen containing groups (hydroxyl, carbonyl, carboxyl) on the nanotube surface which electrostatically stabilize them in water and which can later be utilized in chemical functionalization. One report [56] reveals that the oxygen containing groups in actuality combine with carbon contaminations absorbed to the nanotube wall that can be removed by a simple base wash. Cleaned nanotubes are reported to have reduced D/G ratio indicative of less functionalization, and the absence of oxygen is also apparent from IR spectroscopy and X-ray photoelectron spectroscopy.

Experimental purification strategies

[edit]

A recent kilogram-scale fullerene purification strategy was demonstrated by Nagata et al.[57] In this method C60 was separated from a mixture of C60, C70 and higher fullerene compounds by first adding the amidine compound DBU to a solution of the mixture in 1,2,3-trimethylbenzene. DBU as it turns out only reacts to C70 fullerenes and higher which reaction products separate out and can be removed by filtration. C60 fullerenes do not have any affinity for DBU and are subsequently isolated. Other diamine compounds like DABCO do not share this selectivity.

C60 but not C70 forms a 1:2 inclusion compound with cyclodextrin (CD). A separation method for both fullerenes based on this principle is made possible by anchoring cyclodextrin to colloidal gold particles through a sulfur-sulfur bridge.[58] The Au/CD compound is very stable and soluble in water and selectively extracts C60 from the insoluble mixture after refluxing for several days. The C70 fullerene component is then removed by simple filtration. C60 is driven out from the Au/CD compound by adding adamantol which has a higher affinity for the cyclodextrin cavity. Au/CD is completely recycled when adamantol in turn is driven out by adding ethanol and ethanol removed by evaporation; 50 mg of Au/CD captures 5 mg of C60 fullerene.

See also

[edit]

References

[edit]
  1. ^ a b Hirsch, A.; Bellavia-Lund, C., eds. (1993). Fullerenes and Related Structures (Topics in Current Chemistry). Berlin: Springer. ISBN 3-540-64939-5.
  2. ^ Diederich, F. N. (1997). "Covalent fullerene chemistry". Pure and Applied Chemistry. 69 (3): 395–400. doi:10.1351/pac199769030395.
  3. ^ Prato, M. (1997). "[60]Fullerene chemistry for materials science applications" (PDF). Journal of Materials Chemistry. 7 (7): 1097–1109. doi:10.1039/a700080d.
  4. ^ Beavers, C. M.; Zuo, T.; Duchamp, J. C.; Harich, K.; Dorn, H. C.; Olmstead, M. M.; Balch, A. L. (2006). "Tb3N@C84: An Improbable, Egg-Shaped Endohedral Fullerene that Violates the Isolated Pentagon Rule". Journal of the American Chemical Society. 128 (35): 11352–11353. doi:10.1021/ja063636k. PMID 16939248.
  5. ^ Xie, SY; Gao, F; Lu, X; et al. (2004). "Capturing the Labile Fullerene[50] as C50Cl10". Science. 304 (5671): 699. doi:10.1126/science.1095567. PMID 15118154. S2CID 39189162.
  6. ^ Weng, Q. H.; He, Q.; Liu, T.; Huang, H. Y.; Chen, J. H.; Gao, Z. Y.; Xie, S. Y.; Lu, X.; Huang, R. B.; Zheng, L. S. (2010). "Simple Combustion Production and Characterization of Octahydro[60]fullerene with a Non-IPR C60 Cage". Journal of the American Chemical Society. 132 (43): 15093–15095. doi:10.1021/ja108316e. PMID 20931962.
  7. ^ Prato, M.; Lucchini, V.; Maggini, M.; Stimpfl, E.; Scorrano, G.; Eiermann, M.; Suzuki, T.; Wudl, F. (1993). "Energetic preference in 5,6 and 6,6 ring junction adducts of C60: Fulleroids and methanofullerenes". Journal of the American Chemical Society. 115 (18): 8479. doi:10.1021/ja00071a080.
  8. ^ Vogel, E. (1982). "Recent advances in the chemistry of bridged annulenes". Pure and Applied Chemistry. 54 (5): 1015–1039. doi:10.1351/pac198254051015.
  9. ^ "Synthesis of 6,9,12,15,18-pentamethyl-1,6,9,12,15,18-hexahydro(c60-ih)[5,6]fullerene". Organic Syntheses. 83: 80. 2006.
  10. ^ Iwashita, A.; Matsuo, Y.; Nakamura, E. (2007). "AlCl3-Mediated Mono-, Di-, and Trihydroarylation of [60]Fullerene". Angewandte Chemie International Edition. 46 (19): 3513–6. doi:10.1002/anie.200700062. PMID 17385815.
  11. ^ Hoke, S. H.; Molstad, J.; Dilettato, D.; Jay, M. J.; Carlson, D.; Kahr, B.; Cooks, R. G. (1992). "Reaction of fullerenes and benzyne". The Journal of Organic Chemistry. 57 (19): 5069. doi:10.1021/jo00045a012.
  12. ^ Darwish, A. D.; Avent, A. G.; Taylor, R.; Walton, D. R. M. (1996). "Reaction of benzyne with [70]fullerene gives four monoadducts: Formation of a triptycene homologue by 1,4-cycloaddition of a fullerene". Journal of the Chemical Society, Perkin Transactions 2 (10): 2079. doi:10.1039/P29960002079.
  13. ^ Talyzin, A. V.; Tsybin, Y. O.; Purcell, J. M.; Schaub, T. M.; Shulga, Y. M.; Noréus, D.; Sato, T.; Dzwilewski, A.; Sundqvist, B.; Marshall, A. G. (2006). "Reaction of Hydrogen Gas with C60at Elevated Pressure and Temperature: Hydrogenation and Cage Fragmentation†". The Journal of Physical Chemistry A. 110 (27): 8528–8534. Bibcode:2006JPCA..110.8528T. doi:10.1021/jp0557971. PMID 16821837.
  14. ^ a b c d e f g King, R. (2005). Encyclopedia of Inorganic Chemistry [10 Volumes]. Wiley. pp. 603–625. ISBN 9780470860786.
  15. ^ Chiang, L. Y.; Swirczewski, J. W.; Hsu, C. S.; Chowdhury, S. K.; Cameron, S.; Creegan, K. (1992). "Multi-hydroxy additions onto C60 fullerene molecules". Journal of the Chemical Society, Chemical Communications (24): 1791. doi:10.1039/C39920001791.
  16. ^ Chiang, L. Y.; Upasani, R. B.; Swirczewski, J. W.; Soled, S. (1993). "Evidence of hemiketals incorporated in the structure of fullerols derived from aqueous acid chemistry". Journal of the American Chemical Society. 115 (13): 5453. doi:10.1021/ja00066a014.
  17. ^ Li, J.; Takeuchi, A.; Ozawa, M.; Li, X.; Saigo, K.; Kitazawa, K. (1993). "C60 fullerol formation catalysed by quaternary ammonium hydroxides". Journal of the Chemical Society, Chemical Communications (23): 1784. doi:10.1039/C39930001784.
  18. ^ Wang, S.; He, P.; Zhang, J. M.; Jiang, H.; Zhu, S. Z. (2005). "Novel and Efficient Synthesis of Water‐Soluble [60]Fullerenol by Solvent‐Free Reaction". Synthetic Communications. 35 (13): 1803. doi:10.1081/SCC-200063958. S2CID 96782160.
  19. ^ Zhang, G.; Liu, Y.; Liang, D.; Gan, L.; Li, Y. (2010). "Facile Synthesis of Isomerically Pure Fullerenols and Formation of Spherical Aggregates from C60(OH)8". Angewandte Chemie International Edition. 49 (31): 5293–5. doi:10.1002/anie.201001280. PMID 20575126.
  20. ^ Kokubo, K.; Matsubayashi, K.; Tategaki, H.; Takada, H.; Oshima, T. (2008). "Facile Synthesis of Highly Water-Soluble Fullerenes More Than Half-Covered by Hydroxyl Groups". ACS Nano. 2 (2): 327–333. doi:10.1021/nn700151z. PMID 19206634.
  21. ^ Jia, J.; Wu, H. S.; Xu, X. H.; Zhang, X. M.; Jiao, H. (2008). "Fused Five-Membered Rings Determine the Stability of C60F60". Journal of the American Chemical Society. 130 (12): 3985–3988. doi:10.1021/ja0781590. PMID 18311972.
  22. ^ Yamada, Michio (2013). "Carbene Additions to Fullerenes". Chemical Reviews. 113 (9): 7209–7264. doi:10.1021/cr3004955. PMID 23773169.
  23. ^ Tsuda, Minoru (1993). "C61Cl2. Synthesis and characterization of dichlorocarbene adducts of C60". Tetrahedron Letters. 34 (43): 6911–6912. doi:10.1016/S0040-4039(00)91828-8.
  24. ^ Tzirakis, Manolis D. (2013). "Radical Reactions of Fullerenes: From Synthetic Organic Chemistry to Materials Science and Biology". Chemical Reviews. 113 (7): 5262–5321. doi:10.1021/cr300475r. PMID 23570603.
  25. ^ Morton, J. R. (1992). "ESR studies of the reaction of alkyl radicals with fullerene (C60)". The Journal of Physical Chemistry. 96 (9): 3576–3578. doi:10.1021/j100188a006.
  26. ^ Cortés-Figueroa, J. E. (2003). "An Experiment for the Inorganic Chemistry Laboratory: The Sunlight-Induced Photosynthesis of (η2-C60)M(CO)5 Complexes (M = Mo, W)". Journal of Chemical Education. 80 (7): 799. Bibcode:2003JChEd..80..799C. doi:10.1021/ed080p799.
  27. ^ Vougioukalakis, G. C.; Roubelakis, M. M.; Orfanopoulos, M. (2010). "Open-cage fullerenes: Towards the construction of nanosized molecular containers". Chemical Society Reviews. 39 (2): 817–844. doi:10.1039/b913766a. PMID 20111794.
  28. ^ Roubelakis, M. M.; Vougioukalakis, G. C.; Orfanopoulos, M. (2007). "Open-Cage Fullerene Derivatives Having 11-, 12-, and 13-Membered-Ring Orifices: Chemical Transformations of the Organic Addends on the Rim of the Orifice". The Journal of Organic Chemistry. 72 (17): 6526–6533. doi:10.1021/jo070796l. PMID 17655360.
  29. ^ Hummelen, J. C.; Prato, M.; Wudl, F. (1995). "There is a Hole in My Bucky" (PDF). Journal of the American Chemical Society. 117 (26): 7003. doi:10.1021/ja00131a024. S2CID 97064951.
  30. ^ Vostrowsky, O.; Hirsch, A. (2006). "Heterofullerenes". Chemical Reviews. 106 (12): 5191–5207. doi:10.1021/cr050561e. PMID 17165685.
  31. ^ Hummelen, Jan C.; Bellavia-Lund, Cheryl; Wudl, Fred (1999). "Heterofullerenes. Fullerenes and Related Structures". Topics in Current Chemistry. 199: 93–134. doi:10.1007/3-540-68117-5_3.
  32. ^ Chai, Y.; Guo, T.; Jin, C.; Haufler, R. E.; Chibante, L. P. F.; Fure, J.; Wang, L.; Alford, J. M.; Smalley, R. E. (1991). "Fullerenes with metals inside". The Journal of Physical Chemistry. 95 (20): 7564. doi:10.1021/j100173a002.
  33. ^ Muhr, H. -J.; Nesper, R.; Schnyder, B.; Kötz, R. (1996). "The boron heterofullerenes C59B and C69B: Generation, extraction, mass spectrometric and XPS characterization". Chemical Physics Letters. 249 (5–6): 399. Bibcode:1996CPL...249..399M. doi:10.1016/0009-2614(95)01451-9.
  34. ^ Averdung, J.; Luftmann, H.; Schlachter, I.; Mattay, J. (1995). "Aza-dihydro[60]fullerene in the gas phase. A mass-spectrometric and quantumchemical study". Tetrahedron. 51 (25): 6977. doi:10.1016/0040-4020(95)00361-B.
  35. ^ Lamparth, I.; Nuber, B.; Schick, G.; Skiebe, A.; Grösser, T.; Hirsch, A. (1995). "C59N+ and C69N+: Isoelectronic Heteroanalogues of C60 and C70". Angewandte Chemie International Edition in English. 34 (20): 2257. doi:10.1002/anie.199522571.
  36. ^ Christian, J. F.; Wan, Z.; Anderson, S. L. (1992). "O++C60•C60O+ production and decomposition, charge transfer, and formation of C59O+. Dopeyball or [CO@C58]+". Chemical Physics Letters. 199 (3–4): 373. Bibcode:1992CPL...199..373C. doi:10.1016/0009-2614(92)80134-W.
  37. ^ Ohtsuki, T.; Ohno, K.; Shiga, K.; Kawazoe, Y.; Maruyama, Y.; Masumoto, K. (1999). "Formation of As- and Ge-doped heterofullerenes". Physical Review B. 60 (3): 1531. Bibcode:1999PhRvB..60.1531O. doi:10.1103/PhysRevB.60.1531.
  38. ^ Möschel, C.; Jansen, M. (1999). "Darstellung stabiler Phosphor-Heterofullerene im Hochfrequenzofen". Z. Anorg. Allg. Chem. 625 (2): 175–177. doi:10.1002/(SICI)1521-3749(199902)625:2<175::AID-ZAAC175>3.0.CO;2-2.
  39. ^ Pellarin, M.; Ray, C.; Lermé, J.; Vialle, J. L.; Broyer, M.; Blase, X.; Kéghélian, P.; Mélinon, P.; Perez, A. (1999). "Photolysis experiments on SiC mixed clusters: From silicon carbide clusters to silicon-doped fullerenes". The Journal of Chemical Physics. 110 (14): 6927–6938. Bibcode:1999JChPh.110.6927P. doi:10.1063/1.478598.
  40. ^ a b c Billas, I.M.L.; Branz, W.; Malinowski, N.; Tast, F.; Heinebrodt, M.; Martin, T.P.; Massobrio, C.; Boero, M.; Parrinello, M. (1999). "Experimental and computational studies of heterofullerenes". Nanostructured Materials. 12 (5–8): 1071–1076. doi:10.1016/S0965-9773(99)00301-3.
  41. ^ Branz, W.; Billas, I. M. L.; Malinowski, N.; Tast, F.; Heinebrodt, M.; Martin, T. P. (1998). "Cage substitution in metal–fullerene clusters". The Journal of Chemical Physics. 109 (9): 3425. Bibcode:1998JChPh.109.3425B. doi:10.1063/1.477410.
  42. ^ Hummelen, J. C.; Knight, B.; Pavlovich, J.; Gonzalez, R.; Wudl, F. (1995). "Isolation of the Heterofullerene C59N as Its Dimer (C59N)2" (PDF). Science. 269 (5230): 1554–1556. Bibcode:1995Sci...269.1554H. doi:10.1126/science.269.5230.1554. hdl:11370/ffe5ba8c-5336-4aed-9c78-0a26f31d459d. PMID 17789446. S2CID 31270587.
  43. ^ Keshavarz-K, M.; González, R.; Hicks, R. G.; Srdanov, G.; Srdanov, V. I.; Collins, T. G.; Hummelen, J. C.; Bellavia-Lund, C.; Pavlovich, J.; Wudl, F.; Holczer, K. (1996). "Synthesis of hydroazafullerene C59HN, the parent hydroheterofullerene". Nature. 383 (6596): 147. Bibcode:1996Natur.383..147K. doi:10.1038/383147a0. S2CID 4315682.
  44. ^ Nuber, B.; Hirsch, A. (1996). "A new route to nitrogen heterofullerenes and the first synthesis of (C69N)2". Chemical Communications (12): 1421. doi:10.1039/CC9960001421.
  45. ^ Zhang, G.; Huang, S.; Xiao, Z.; Chen, Q.; Gan, L.; Wang, Z. (2008). "Preparation of Azafullerene Derivatives from Fullerene-Mixed Peroxides and Single Crystal X-ray Structures of Azafulleroid and Azafullerene". Journal of the American Chemical Society. 130 (38): 12614–12615. doi:10.1021/ja805072h. PMID 18759401.
  46. ^ Xin, N.; Huang, H.; Zhang, J.; Dai, Z.; Gan, L. (2012). "Fullerene Doping: Preparation of Azafullerene C59NH and Oxafulleroids C59O3 and C60O4". Angewandte Chemie International Edition. 51 (25): 6163–6166. doi:10.1002/anie.201202777. PMID 22573566.
  47. ^ Komatsu, K.; Wang, G. W.; Murata, Y.; Tanaka, T.; Fujiwara, K.; Yamamoto, K.; Saunders, M. (1998). "Mechanochemical Synthesis and Characterization of the Fullerene Dimer C120". The Journal of Organic Chemistry. 63 (25): 9358. doi:10.1021/jo981319t.
  48. ^ Komatsu, K.; Fujiwara, K.; Murata, Y. (2000). "The Mechanochemical Synthesis and Properties of the Fullerene Trimer C180". Chemistry Letters. 29 (9): 1016–1017. doi:10.1246/cl.2000.1016.
  49. ^ Kunitake M, Uemura S, Ito O, Fujiwara K, Murata Y, Komatsu K (2002). "Structural Analysis of C60 Trimers by Direct Observation with Scanning Tunneling Microscopy". Angewandte Chemie International Edition. 41 (6): 969–972. doi:10.1002/1521-3773(20020315)41:6<969::AID-ANIE969>3.0.CO;2-I. PMID 12491284.
  50. ^ Scott, L. T.; Boorum, M. M.; McMahon, B. J.; Hagen, S.; Mack, J.; Blank, J.; Wegner, H.; De Meijere, A. (2002). "A Rational Chemical Synthesis of C60". Science. 295 (5559): 1500–1503. Bibcode:2002Sci...295.1500S. doi:10.1126/science.1068427. PMID 11859187. S2CID 74269.
  51. ^ The numbers in image correspond to the way the new carbon carbon bonds are formed.
  52. ^ Lungerich, Dominik; Hoelzel, Helen; Harano, Koji; Jun, Norbert; Amsharov, Konstantin; Nakamura, Eiichi (2021). "A Singular Molecule-to-Molecule Transformation on Video: The Bottom-Up Synthesis of Fullerene C60 from Truxene Derivative C60H30". ACS Nano. 15 (8): 12804–12814. doi:10.1021/acsnano.1c02222. PMID 34018713. S2CID 235074316.
  53. ^ Amsharov, K. Y.; Jansen, M. (2008). "A C78 Fullerene Precursor: Toward the Direct Synthesis of Higher Fullerenes". The Journal of Organic Chemistry. 73 (7): 2931–2934. doi:10.1021/jo7027008. PMID 18321126.
  54. ^ Kabdulov, M.; Jansen, M.; Amsharov, K. Yu (2013). "Bottom-Up C60 Fullerene Construction from a Fluorinated C60H21F9 Precursor by Laser-Induced Tandem Cyclization". Chem. Eur. J. 19 (51): 17262–17266. doi:10.1002/chem.201303838. PMID 24273113.
  55. ^ Spencer, T.; Yoo, B.; Kirshenbaum, K. (2006). "Purification and Modification of Fullerene C60 in the Undergraduate Laboratory". Journal of Chemical Education. 83 (8): 1218. Bibcode:2006JChEd..83.1218S. doi:10.1021/ed083p1218.[permanent dead link]
  56. ^ Verdejo, R.; Lamoriniere, S.; Cottam, B.; Bismarck, A.; Shaffer, M. (2007). "Removal of oxidation debris from multi-walled carbon nanotubes". Chemical Communications (5): 513–5. doi:10.1039/b611930a. PMID 17252112.
  57. ^ Nagata, K.; Dejima, E.; Kikuchi, Y.; Hashiguchi, M. (2005). "Kilogram-scale [60]Fullerene Separation from a Fullerene Mixture: Selective Complexation of Fullerenes with 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)". Chemistry Letters. 34 (2): 178. doi:10.1246/cl.2005.178.[permanent dead link]
  58. ^ Liu, Y.; Yang, Y. W.; Chen, Y. (2005). "Thio[2-(benzoylamino)ethylamino]-β-CD fragment modified gold nanoparticles as recycling extractors for [60]fullerene" (PDF). Chemical Communications (33): 4208–10. doi:10.1039/b507650a. PMID 16100605. Archived from the original (PDF) on 2016-03-04. Retrieved 2015-08-29.
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