Polyfullerene

Add links
From Wikipedia, the free encyclopedia
This article is about homopolymer and polymers consisting of  Buckminsterfullerene (C60). For information about fullerene, see Fullerene.

Polyfullerene is a basic polymer of the C60 monomer group, in which fullerene segments are connected via covalent bonds into a polymeric chain without side or bridging groups. They are called intrinsic polymeric fullerenes, or more often all C60 polymers.

Fullerene can be part of a polymer chain in many different ways. Fullerene-containing polymers are divided into following structural categories:

History[edit]

Fullerene is a relatively new substance in chemistry sciences. Buckminsterfullerene itself was discovered in 1985[1] and the first fullerene-containing polymers were reported at least 6[2] years later.

The main milestones in the use of fullerene in polymer chemistry are listed below:

  • 1992 – Synthesis of organometallic C60 polymer (C60Pd3)n[3]
  • 1995 – Synthesis of C60 containing polyurethane[4] and C60-styrene copolymer[5]
  • 1996 – Synthesis of fullerene side-chain polymer[6]
  • 1997 – Synthesis of fullerene polymer with C60 in the backbone by Diels-Alder reaction
  • 2001 – Synthesis of star-shaped C60 (co)polymers[7]
Schematic of polyfullerene grid
Schematic of polyfullerene grid

Fullerene polymers[edit]

High content of double bonds in the fullerene molecule (30 double bonds in Buckminsterfullerene) leads to crosslinking and formation of regioisomers. Polymerization without any sophisticated control of forming structure leads to very high randomization of polymer grid. Thus, linking units of second monomer are needed to prepare linear copolymers (see main-chain polymers).

This group includes heteroatomic C60 polymers containing non-carbon atoms in polyfullerene chains.[8]

Preparations[edit]

This section describes most of the main structural types of fullerene-containing polymers.

Homopolymer[edit]

Polyfullerenes can be prepared via many polymerization mechanisms. Research is mainly focused on photopolymerization,[9] polymerization under high pressure[10] and charge-transfer polymerization.[11]

The most likely connection of fullerene units is [2+2] cycloaddition of two double bonds of the benzene parts of fullerene molecules. Cycloaddition provides a cyclobutane ring connecting two fullerene molecules.[12][13]

C60 Buckminsterfullerene polymeric bond
Photopolymerization of C60 Buckminsterfullerene forming cyclobutane bond via [2+2] cycloadition

Main-chain polymers[edit]

Main-chain polymers are characterized by the presence of fullerene units in the polymer backbone. They are not heteroatomic fullerene homopolymers but linear fullerene copolymers.

The structure can be described as necklace-type. One approach to achieving fullerene main-chain polymers is by copolymerizing fullerene with a difunctional monomer. Second option is polycondensation of bifunctionalized fullerene with monomer bearing compatible functional groups.

Scheme of synthetic approaches for obtaining fullerene main-chain polymers.
Scheme of synthetic approaches for obtaining fullerene main-chain polymers.

Fullerene copolymers can be obtained through standard polymerization techniques used for industrially standard polymers. Examples of first approach are Diels-Alder addition and free radical copolymerization. Fullerene can be copolymerized with methylmethacrylate by initiation with azobisisobutyronitrile (AIBN).[14]

Free radical copolymerization of methylmethacrylate and C60 Buckminsterfullerene
Free radical copolymerization of methylmethacrylate and C60 Buckminsterfullerene

In Diels-Alder copolymerization fullerene acts as a dienophile with diene to form a cyclohexene ring. The figure below shows Diels-Alder reaction with the simplest diene – buta-1,3-diene. Comonomer must contain two pairs of conjugated double bonds in order to react with two fullerene molecules obtaining linear polymeric chain molecules. Used monomers are usually bulkier than conventional monomers in order to compensate the space requirements of fullerene spheres.

Diels-Alder reaction of C60 Buckminsterfullerene with buta-1,3-diene.

Side-chain polymers[edit]

Most fullerene polymers fall into this category.[8] Similarly to the previous polymer type, two synthetic approaches are available. First, bonding fullerene spheres onto a polymerized chain or second, polymerizing monomer unit already bearing fullerene.

Scheme of synthetic approaches for obtaining fullerene side-chain polymers.
Scheme of synthetic approaches for obtaining fullerene side-chain polymers.

An example of the second approach is ring-opening metathesis polymerisation (ROMP) of norbornene bearing C60 or copolymerization of pure norbornene and C60 functionalized norbornene[15].

Ring Opening Methatesis Polymerization (ROMP) of C60 Buckminsterfullerene functionalized norbornene.
Ring Opening Methatesis Polymerization (ROMP) of C60 Buckminsterfullerene functionalized norbornene.

Cross-linked polymers[edit]

As mentioned earlier, Buckminsterfullerene is capable of multiple additions and basic polymerization conditions lead to a polymer grid. Fullerene behaves the same way in copolymerization. In free radical copolymerization of styrene and C60 fullerene, the resulting copolymer is cross-linked and heterogeneous.[16]

Easy preparation of cross-linked fullerene polymer is copolymerization with polyurethanes. In this technique, fullerenol bearing up to 44 hydroxyl groups C60(OH)4 – 44[17] and di- or tri- isocyanate prepolymers are used as initial substances. Successful syntheses were conducted in a mixture of dimethylformamide (DMF) and tetrahydrofuran (THF)(1:3) at 60°C.[18]

Fullerene End-caped polymers

Also incorrectly named “telechelic” polymers, but telechelic polymers have reactive functional end-groups. They can be synthesized by incorporating fullerenes onto the ends of polymerized chains or growth of a polymeric chain from a functionalized fullerene derivative and additionally closure. Introducing fullerene spheres into the end of the macromolecule significantly increases hydrophobicity of the original polymer.

Scheme of synthetic approaches for obtaining fullerene end-caped polymers.
Scheme of synthetic approaches for obtaining fullerene end-caped polymers.

Star-shaped polymers[edit]

Star fullerene polymers can be prepared by two major approaches.

Reported star fullerene polymers were prepared by anionic copolymerization with polystyrene to form C60(CH2CH(C6H5))x)n, where n stands for the number of polystyrene star “arms” from 2 to 6.[19][20] Second approach is growing polymer chains directly from fullerene derivative C60Cln (n = 16–20) by atom transfer radical polymerization. The chlorine fullerene derivative virtually works as an ATRP initiator. Countless polymers can be used for star arms.

Polyphenylakyne polymers can be used as an example since they give photoemitting macromolecules when grafted onto fullerene. C60-poly(1-phenyl-1-propyne) can be prepared via wolfram-catalyzed metathesis reaction connecting prepared poly(1-phenyl-1-propyne) onto the fullerene by carbene addition resulting in cyclopropane connecting ring.[21] Fullerene acts as a cocatalyst since tungsten catalyst (WCl6-Ph4Sn) is not able to polymerize 1-phenyl-1-propyne itself.

Copolymerization of 1-phenyl-1-propyne with C60 Buckminsterfullerene catalyzed by tungsten.
Copolymerization of 1-phenyl-1-propyne with C60 Buckminsterfullerene catalyzed by tungsten catalyst.

Applications[edit]

Polyfullerenes are currently in an early research phase and real-world applications or even industrial production solutions are yet to be found. The main reasons for this are the novelty of combining fullerene chemistry with polymer chemistry and the fact that fullerene can be currently synthesized on a scale of a few grams. All-C60 polymers exhibit practically no solubility, thus preventing proper testing of processability and chemical properties.

Upcoming text only refers to potential applications of fullerene polymers according to founded properties of particular macromolecules.

Electronics[edit]

Fullerene itself stands out in the class of organic compounds because of its electronic properties. Current research studies utilization of fullerene by bonding it onto an optimal polymeric substrate. Practical reasons are easy processability of polymers and low price in comparison to pure C60 fullerene.

Polymer backbones bearing fullerene spheres exhibit good or great photoconductivity and even generate photocurrent when exposed to white light.[22][23]

C60-polyvinylcarbazole (C60–PVK) exhibits photoinduced electron transfer within the polymer, which could be used for digital rewritable memory electronic parts. Prototype of such part of indium tin oxide, fullerene polymer and aluminum (ITO/ C60–PVK /Al) was capable to read, write and erase information for about 100 million times.[24]

Polyvinylcabazole polymer grown from fullerene polychloride (C60Cln) was observed to increase the intensity of radiated light of an electroluminescent device. This star polymer with three arms is acting as a hole-transporting layer for semiconductor parts of a device.[25]

On the other hand, hole-trapping materials affect electroluminescence the same way. Double-cable polymers are also candidates for functional layers for OLED displays. Adding 1 wt. % into basic OLED material increased luminescence of the diode.[26] Very promising hole-trapping materials are polyacetylene backbone polymers with fullerene in combination with different electron-accepting groups in branches.[27]

Star copolymer (PS)xC60(PMMA)y (polystyrene and polymethylmethacrylate being different star “arms”) acted as an active electroluminescence layer. It improved emitting of a semiconductor electroluminescence device by up to 20 times.[28] C60-poly(1-phenyl-1-propyne) is also reported to exhibit light emission.[29] Fullerene moiety increased emission of blue light two times in comparison to pure poly(phenyl propyne). Stability and processability of such polymer is very good.

Solar panels[edit]

C60 Buckminsterfullerene-functionalised styrene side-chain homopolymer.
C60 Buckminsterfullerene-functionalised styrene side-chain homopolymer.

Fullerene polymers are widely studied in organic solar cells for active layers of new-generation photovoltaic panels. Examples are homopolymers of C60-polystyrene[30] and C60-polyethyleneglycols[31] or C60 copolymers prepared by ROMP polymerization.[32][33] The current efficiency of converting incoming sun radiation to electricity is about 3%.[32]

Another polymer type with intrinsic properties are “Double-Cable” polymers. They are brush-like structures consisting of 𝜋-electron conjugated backbone (P-type part) bearing electron-accepting branches (N-type part).[34][35]

Optical limiting properties[edit]

Particular fullerene (co)polymers exhibit an optical limiting property, meaning they block intense light flux passing through them. Low intensity light flux is not affected. It is useful for light control parts in optics and as sensor or eye protection.[36][37][38][39]

Surface activity[edit]

Currently, fullerene copolymerized with palladium showed some practical aspects, particularly (C60Pd3)n due to the content of palladium on its surface, exhibits catalytic effect for hydrogenation of alkenes[40] and can lead to the development of new catalytic systems and products.

(C60Pd)n polymers can adsorb gases, making them useful as adsorbents for volatile and toxic species. For example, a great affinity to toluene was proved.[41] The palladium atoms in the backbone are partially positive and thus attract 𝜋-electrons of aromatic core of toluene.

Introducing correct amount of fullerene as side groups onto poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) increases permeability of gas separation membranes by 80 % in comparison with pure PPO. Bulky fullerene probably increases the free volume of PPO.[42]

Exceptional mechanical properties[edit]

Materials originating from polyurethane synthesis exhibit improved thermal mechanical stability.[43] Fullerene-containing polyurethanes also exhibit strong optical response and are potentially applicable for optical signal processing.[38]

Linear polymer chains containing fullerene undergo crosslinking. Resulting material exhibits elastomeric behavior with 10 times higher tensile strength and 17 times higher elongation at break than the same material without fullerene.[8]

Blending of fullerene end-capped polymers (polyethylene glycols for example) with H-donating polymers (polyvinylchloride, poly(p-vinyl phenol), polymethylmethacrylate, etc.) leads to the enhancement of mechanical properties of H-donating polymers.

Scavengers of free radicals[edit]

Fullerene end-caped poly(N-isopropylacrylamide) is a water-soluble polymer with the tendency to form clusters.[44] It is a very good scavenger of free radicals, and it can be used for controlling radical polymerizations.

Depolymerizeable polymers[edit]

Fullerene polymers are potential candidates for establishing polymer circular economy.

Depolymerizeable polymers are the hope of polymer recycling. C60 fullerene copolymerized with [4,4′-bithiazole]-2,2′-bis(diazonium)chloride (see Magnetic behavior) was observed to depolymerize in a temperature range of 60-75°C. Polymerization and depolymerization can be done several times before degradation of initial components.[45] The depolymerization temperature and the difference between polymerization and depolymerization temperatures must be increased.

Cancer treatment[edit]

Basic fullerene polymers without polar functional groups are strongly hydrophobic, thus incompatible for medicinal use in the human body.

An example of water-soluble derivatives are polyfullerocyclodextrins. They are prepared by reaction of 𝛽-cyclodextrin complexes with fullerene. They exhibit excellent DNA-cleaving activity[46] (in the presence of visible light, they cleave DNA quantitatively). This phenomenon can be used for eliminating cancer cells.

The introduction of hydrophilic groups into the macromolecule is the principle of preparing water-soluble polymers. Examples of backbones for water-soluble fullerene side-chain polymers are for example poly(maleic anhydride-co-vinyl acetate) (52) or pullulan.[47]

Magnetic behavior[edit]

Polymers with C60-backbone with ferromagnetic properties were reported in literature,[48] although fullerene itself is antiferromagnetic. An example of a successful synthesis of ferromagnetic C60–polymer uses [4,4′-bithiazole]-2,2′-bis(diazonium)dichloride, C60 and FeSO4.

Soft magnetic copolymer of bithiazole derivative and C60 Buckminsterfullerene.
Soft magnetic copolymer of bithiazole derivative and C60 Buckminsterfullerene.

References[edit]

  1. ^ "Fullerene", Wikipedia, 2022-12-16, retrieved 2023-06-01
  2. ^ Jeon, I. Ch.; Hwang, S. Y.; Bang, G. S.; Lee, G. H.; Kim, S. S.; et al. Fullerenes. Part 2. Photochemical formation of polymer-bound C60. Bulletin of the Korean Chemical Society 1991, 12 (6), 596–8.
  3. ^ H. Nagashima, A. Nakaoka, Y. Saito, M. Kato, T. Kawanishi, and K. Itoh, J. Chem. Soc., Chem. Commun. 377 (1992)
  4. ^ Chiang L. Y.; Wang L. Y. and Kuo C.-S. Macromolecules 28, 7574 (1995).
  5. ^ Christine W.; Christian F.; Rolf M. and Holger F. Fullerene-End-Capped Polystyrenes. Monosubstituted Polymeric C60 Derivatives. Macromolecules 1995 28 (1), 403-405
  6. ^ Sun Y.-P.; Lawson G. E.; Huang W.;Wright A. D. and Moton D. K. Macromolecules 32, 8747 (1999).
  7. ^ Koudoumas E.; Konstantaki M.; Mavromanolakis A.; Couris S.; Ederle ́ Y.; Mathis C.; Seta P. and Leach S. Chem. Phys. Lett. 335, 533 (2001).
  8. ^ a b c Giacalone, Francesco; Martín, Nazario (2007-10-15), "Fullerene Polymers: Synthetic Strategies, Properties and Applications", in John Wiley & Sons, Inc. (ed.), Encyclopedia of Polymer Science and Technology, Hoboken, NJ, USA: John Wiley & Sons, Inc., doi:10.1002/0471440264.pst553, ISBN 978-0-471-44026-0, retrieved 2023-06-01
  9. ^ Pusztai T.; Oszlányi G.; Faigel G.; Kamarás K.; Gránásy L. and S. Pekker. SolidState Commun. 111, 595 (1999).
  10. ^ Iwasa, Y.; Arima, T.; Fleming, R. M.; Siegrist, T.; Zhou, O.; et al. Science 1994, 264, 1570.
  11. ^ Rao, A. M.; Eklund, P. C.; Venkateswaran, U. D.; Tucker, J.; Duncan, M. A.; et al. A, (1997). Appl. Phys. A 1994, 64 (231).
  12. ^ Kratschmer, W.; Lamb, L. D.; Fostiropoulos, K.; Huffman, D. R. W., L. D., K., and D. R.. Nature 1990, 347 (354)
  13. ^ Nuñez-Regueiro, M.; Marques, L.; Hodeau, J. L.; Béthoux, O.; Perroux, M. Phys. Rev. Lett. 1995, 74 (278).
  14. ^ Lu, Z.; Goh, S. H.; Lee, S. Y.; Sun, X. and Ji, W. Polymer 1999, 40 (2863).
  15. ^ Chiang, L. Y.; Bhonsle, J. B.; Wang, L.; Shu, S. F.; Chang, T. M.; Hwu, J. R. Tetrahedron 1996, 52, 4963.
  16. ^ Bunker, C. E.; Lawson, G. E.; Sun, Y. P. Macromolecules 1995, 28, 3744.
  17. ^ Eropkin, M. Yu.; Melenevskaya, E. Yu.; Nasonova, K. V.; Bryazzhikova, T. S.; Eropkina, E. M.; Danilenko, D. M.; Kiselev, O. I. (2013-05-01). "Synthesis and Biological Activity of Fullerenols with Various Contents of Hydroxyl Groups". Pharmaceutical Chemistry Journal. 47 (2): 87–91. doi:10.1007/s11094-013-0901-x. ISSN 1573-9031. S2CID 254888848.
  18. ^ Chiang, L. Y.; Wang, L. Y.; Kuo, C. S. Macromolecules 1995, 28, 7574.
  19. ^ Venturini, J.; Koudoumas, E.; Couris, S.; Janot, J. M.; et al. J. Mater. Chem. 2002, 12 (2071).
  20. ^ Koudoumas, E.; Konstantaki, M.; Mavromanolakis, A.; Couris, S.; Ederlé, Y.; et al. Chem. Phys. Lett. 2001, 335 (533).
  21. ^ Tang, B. Z.; Xu, H.; Lam, J. W. Y.; Lee, P. P. S.; et al. Chem. Mater. 2000, 12 (1446).
  22. ^ Wang, C.; Tao, Z.; Yang, W.; Fu, S. Macromol. Rapid Commun. 2001, 22, 98.
  23. ^ Wang, N.; Lu, F.; Huang, C.; Li, Y.; et al. J. Polym. Sci., Part A: Polym. Chem. 2006, 44, 5836.
  24. ^ Ling, Q. D.; Lim, S. L.; Song, Y.; Zhu, C. X.; et al. Langmuir 2007, 23, 584.
  25. ^ Park, J. H.; Park, O. O.; Kim, J.; ou, J. W.; Kim, J. K.; Kim, Y. C. Curr. Appl. Phys. 2004, 4, 659.
  26. ^ Yang, C.; Li, H.; Sun, Q.; Qiao, J.; Li, Y.; Li, Y.; Zhu and D. Sol. Energy Mater. Sol. Cells 85, 2005, 241.
  27. ^ Liu, Y.; Wang, N.; Li, Y.; et al. Macromolecules 2005, 38, 4880.
  28. ^ Lee, T. W.; Park, O. O.; Kim, J.; Kim, Y. C. Chem Mater. 2002, 14, 4281.
  29. ^ Tang, B. Z.; Xu, H.; Lam, J. W. Y.; Lee, P. P. S.; Xu, K.; Sun, Q.; Cheuck, K. K. L. Chem. Mater. 2000, 12, 1446.
  30. ^ Adamopoulos, G.; Heiser, T.; Giovannella, U.; et al. Thin Solid Films 2006, 371, 511–512.
  31. ^ Gutiérrez-Nava, M.; Setayesh, S.; Rameau, A.; Masson, P.; Nierengarten, J. F.; et al. New J. Chem. 2002, 26, 584.
  32. ^ a b Ball, Z. T.; Sivula, K.; Fréchet, J. M. J.; et al. Macromolecules 2006, 39, 70.
  33. ^ De la Escosura, A.; Martínez-Díaz, M. V.; Torres, T.; Grubbs, R. H.; et al. Chem. Asian J. 2007, 1-2, 148.
  34. ^ Jousselme, B.; Blanchard, P.; Levillain, E.; de Bettignies, R.; Roncali, J. Macromolecules 2003, 36, 3020.
  35. ^ Zhang, F.; Svensson, M.; Andersson, M. R.; Maggini, M.; Bucella, S.; Menna, E.; Inganäs, O. Adv. Mater. 2001, 13, 1871.
  36. ^ Sooraj, Bhuvanachandran Nair Sreekala; Pradeep, Thalappil (2023-01-01), Pradeep, Thalappil (ed.), "Chapter 4 - Optical properties of metal clusters", Atomically Precise Metal Nanoclusters, Elsevier, pp. 83–101, doi:10.1016/b978-0-323-90879-5.00010-x, ISBN 978-0-323-90879-5, retrieved 2023-06-02
  37. ^ Zhang, T.; Xi, K.; Yu, X.; Gu, M.; Guo, S.; Gu, B.; Wang, H. Polymer 2003, 44, 2647.
  38. ^ a b Bunker, C. E.; Lawson, G. E.; Sun, Y. P. Macromolecules 1995, 28, 3744.
  39. ^ Koudoumas, E.; Konstantaki, M.; Mavromanolakis, A. Chem. Phys. Lett. 2001, 335, 533.
  40. ^ Nagashima, H.; Nakaoka, A.; Saito, Y.; Kato, M.; Kawanishi, T.; Itoh, K. J. Chem. Soc., Chem. Commun. 1992, 377.
  41. ^ Hebard, A. F. Annu. Rev. Mater. Sci. 1993, 23, 159.
  42. ^ Goh, S. H.; Zheng, J. W.; Lee, S. Y. Polymer 2000, 41, 8721.
  43. ^ Luang, L.; Chen, Q.; Sargent, E. H.; Wang, Z. Y. J. Am. Chem. Soc. 2003, 125, 13648.
  44. ^ Zhou, G.; Harruna, I. I.; Zhou, W. L.; Aicher, W. K.; Geckeler, K. E. Chem. Eur. J.2007, 13, 569.
  45. ^ Nie, B.; Rotello, V. M. Macromolecules 1997, 30, 3949.
  46. ^ ass, H. I. J. Natl. Cancer Inst. 1993, 85, 443.
  47. ^ Okamura, H.; Miyazono, K.; Minoda, M.; Miyamoto, T. Macromol. Rapid Commun.1999, 20, 41.
  48. ^ Jiang, L.; Sun, W.; Weng, J.; Shen, Z. Polymer 2002, 43, 1563.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Polyfullerene&oldid=1195116186"