Linear acetylenic carbon

Linear acetylenic carbon (LAC), also called carbyne, is an allotrope of carbon that has the chemical structure (−C≡C−)_n as a repeating chain, with alternating single and triple bonds.^[1][2] It would thus be the ultimate member of the polyyne family.

This type of carbyne is of considerable interest to nanotechnology as its Young's modulus is 7013327000000000000♠32.7 TPa – forty times that of diamond.^[3] It has also been identified in interstellar space; however, its existence in condensed phases has been contested recently, as such chains would crosslink exothermically (and perhaps explosively) if they approached each other.^[4]

History and controversy

The first claims of detection of this allotrope were made by V. I. Kasatochkin, Y. P. Kudryavtsev and others in 1960^[4][5] and repeated in 1978.^[6] In 1982 P. P. K. Smith and P. R. Buseck re-examined samples from several previous reports and showed that the signals attributed to carbyne were in fact due to silicate impurities in the samples.^[7] Absence of carbyne crystalline rendered the direct observation of a pure carbyne-assembled solid still a major challenge, because carbyne crystals with well-defined structures and sufficient sizes are not available to date. This is indeed the major obstacle to general acceptance of carbyne as a true carbon allotrope. The mysterious carbyne still attracted scientists with its possible extraordinary properties.^[8]

In 1984, a group at Exxon reported the detection of clusters with even numbers of carbons, between 30 and 180, in carbon evaporation experiments, and attributed them to polyyne carbon.^[9] However, these clusters later were identified as fullerenes.^[4]

In 1991, carbyne was allegedly detected among various other allotropes of carbon in samples of amorphous carbon black vaporized and quenched by shock waves produced by shaped explosive charges.^[10]

In 1995, the preparation of carbyne chains with over 300 carbons was reported. They were claimed to be reasonably stable, even against moisture and oxygen, as long as the terminal alkynes on the chain are capped with inert groups (such as tert-butyl or trifluoromethyl) rather than hydrogen atoms. The study claimed that the data specifically indicated a carbyne-like structures rather than fullerene-like ones.^[11] However, according to H. Kroto, the properties and synthetic methods used in those studies are consistent with generation of fullerenes.^[4]

Another 1995 report claimed detection of carbyne chains of indeterminate length in a layer of carbonized material, about 180 nm thick, resulting from the reaction of solid polytetrafluoroethylene (PTFE, Teflon) immersed in alkali metal amalgam at ambient temperature (with no hydrogen-bearing species present).^[12] The assumed reaction was

(−CF
2−CF
2−)_n + 4 M → (−C≡C−)_n + 4 MF,

where M is either lithium, sodium, or potassium. The authors conjectured that nanocrystals of the metal fluoride between the chains prevented their polymerization.

In 1999, F. Cataldo observed that copper(I) acetylide ((Cu+
)₂C2−
2) after partial oxidation by exposure to air or copper(II) ions releases polyynes H(−C≡C−)_nH, with n from 2 to 6, when decomposed by hydrochloric acid, and leaves a "carbonaceous" residue with the spectral signature of (−C≡C−)_n chains. He conjectured that the oxidation causes polymerization of the acetylide anions C2−
2 into carbyne-type anions C(≡C−C≡)_nC²⁻ or cumulene-type anions C(=C=C=)_mC⁴⁻.^[13] Also, thermal decomposition of copper acetylide in vacuum yielded a fluffy deposit of fine carbon powder on the walls of the flask, which, on the basis of spectral data, was claimed to be carbyne rather than graphite.^[13] Finally, the oxidation of copper acetylide in ammoniacal solution (Glaser's reaction) produces a carbonaceous residue that was claimed to consist of "polyacetylide" anions capped with residual copper(I) ions,

Cu+
⁻C(≡C−C≡)_nC⁻ Cu+
.

On the basis of the residual amount of copper, the mean number of units n was estimated to be around 230.^[14]

In 2004, an analysis of a synthesized linear carbon allotrope found it to have a cumulene electronic structure—sequential double bonds along an sp-hybridized carbon chain—rather than the alternating triple–single pattern of linear carbyne.^[15]

The synthesis of linear chains of up to 6,000 sp-hybridized carbon atoms was reported in 2016. The chains were grown inside double-walled carbon nanotubes.^{[16] [17]}

Polyynes

While the existence of "carbyne" chains in pure neutral carbon material is still disputed, short (−C≡C−)_n chains are well established as substructures of larger molecules (polyynes)^[18] and are even synthesized by several living organisms. As of 2010, the longest such chain in a stable molecule had 22 acetylenic units (44 atoms), stabilized by rather bulky end groups.^[19]

Structure

The carbon atoms in this form are each linear in geometry with sp orbital hybridisation. The estimated length of the bonds is 120.7 pm (triple) and 137.9 pm (single).^[12]

Other possible configurations for a chain of carbon atoms include polycumulene (polyethylene-diylidene) chains with double bonds only (128.2 pm). This chain is expected to have slightly higher energy, with a Peierls gap of 2 to 5 eV. For short C
n C_n molecules, however, the polycumulene structure seems favored. When n is even, two ground configurations, very close in energy, may coexist: one linear, and one cyclic (rhombic).^[12]

The limits of flexibility of the carbyne chain are illustrated by a synthetic polyyne with a backbone of 8 acetylenic units, whose chain was found to be bent by 25 degrees or more (about 3 degrees at each carbon) in the solid state, to accommodate the bulky end groups of adjacent molecules.^[20]

The highly symmetric carbyne chain is expected to have only one Raman-active mode with Σ_g symmetry, due to stretching of bonds in each single-double pair, with frequency typically between 1950 and 2300 cm⁻¹.^[12]

Properties

Carbyne chains have been claimed to be the strongest material known per density. Calculations indicate that carbyne’s specific tensile strength (strength divided by density) of 6.0–7007750000000000000♠7.5×10⁷ N·m/kg beats graphene (4.7–7007550000000000000♠5.5×10⁷ N·m/kg), carbon nanotubes (4.3–7007500000000000000♠5.0×10⁷ N·m/kg), and diamond (2.5–7007650000000000000♠6.5×10⁷ N·m/kg).^[21][22][23] Its specific modulus (Young's Modulus divided by density) of around 7009100000000000000♠10⁹ N·m/kg is also double that of graphene, which is around 7008450000000000000♠4.5×10⁸ N·m/kg.^[21][24]

Stretching carbyne 10% alters its electronic band gap from 3.2 to 4.4 eV.^[25] Outfitted with molecular handles at chain's ends, it can also be twisted to alter its band gap. With a 90-degree end-to-end rotation, it becomes a magnetic semiconductor just by stretching the material by 10% and finally, when twisted by 90°, carbyne also turns into a magnetic semiconductor.^[22]

Carbyne chains can take on side molecules that may make the chains suitable for energy^[22] and hydrogen^[26] storage.

The material is stable at room temperature, largely resisting crosslinks with nearby chains. The rods' stiffness prevents them from coming together in a second location, at least at room temperature.^[22]

References

Further reading

• Tobe, Y.; Wakabayashi, T. (2005-03-04). "Chapter 9. Carbon-Rich Compounds: Acetylene-Based Carbon Allotropes". In Diederich, F.; Stang, P. J.; Tykwinski, R. R. Acetylene Chemistry Acetylene chemistry: chemistry, biology, and material science Check |url= value (help). pp. 387–426. ISBN 9783527307814.