Polythiazyl

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Template:Chembox

Polythiazyl (polymeric sulfur nitride), Template:Chem2, is an electrically conductive, gold- or bronze-colored polymer with metallic luster. It was the first conductive inorganic polymer discovered[1][2] and was also found to be a superconductor at very low temperatures (below 0.26 K).[3][4] It is a fibrous solid, described as "lustrous golden on the faces and dark blue-black", depending on the orientation of the sample. It is air stable and insoluble in all solvents.[5]

History

The compound was first reported as early as 1910 by F.P. Burt, who obtained it by heating tetrasulfur tetranitride in vacuum over silver wool.[6]

The compound was the first compound with only non-metallic elements in which superconductivity could be demonstrated. However, the relatively low transition temperature at about 0.3 K makes a practical application unlikely.[7][8]

Properties

Polythiazyl is a metallic-golden and shiny, crystalline but fibrous material.[8] The polymer is mostly inert to oxygen and water, but decomposes in air to a grey powder after months of exposure.[9][10] At temperatures above 240 °C explosive decomposition can occur.[11] The compound also explodes on impact.[10] Explosion generally proceeds via decomposition to the elements.

Polythiazyl shows an anisotropic electrical conductivity. Along the fibres or SN chains, the bond is electrically conductive, perpendicular to it acts as an insulator. The one-dimensional conductivity is based on the bonding conditions in the S-N chain, where each sulfur atom provides two π electrons and each nitrogen atom provides one π electron to form two-center 3π electron bonding units.[8]

Two polymorphic crystal forms were observed in the compound. The monoclinic form I obtained from the synthesis can be converted into an orthorhombic form II by mechanical treatment such as grinding.[12]

Structure and bonding

The material is a polymer, containing trivalent nitrogen, and divalent and tetravalent sulfur. The S and N atoms on adjacent chains align.[2][13][14] Several resonance structures can be written.[15]

Polythiazyl resonance structures

The structure of the crystalline compound was resolved by X-ray diffraction. This showed alternating S–N bond lengths of 159 pm and 163 pm and S–N–S bond angles of 120 ° and N–S–N bond angles of 106 °.[16][17][9][8]

Synthesis

The oldest-known polythiazyl synthesis is the polymerization of the cyclic formal dimer disulfur dinitride (Template:Chem2), which is in turn synthesized from the formal tetramer tetrasulfur tetranitride (Template:Chem2),[2] in the presence of hot silver wool.[2][1][18] The reaction begins when silver abstracts sulfur from Template:Chem2 to produce a Template:Chem2 catalyst; the resulting gaseous Template:Chem2 is then isolated through sublimation onto a cold surface:

S4N4 + 8 Ag → 4 Ag2S + 2 N2
S4N4 (low-pressure gas at 250-300 °C; Ag2S catalyst) → 2 S2N2 (gas) → 2 S2N2 (stable solid at 77 K)

When warmed to room temperature, the additional heat induces spontaneous polymerization:

S2N2 (0 °C) → (SN)x

An alternative is the azide reduction of thiazyl chloride trimer,[19] itself made from thiazyl fluoride:[20]

(NSF)3 + Cl2 → (SNCl)3 + ClF
(SNCl)3 + NaN3 → NaCl + N2 + (SN)∞

To eschew explosive reagents entirely, iron filings in nitromethane reduce the thiazyl chloride trimer to [(SN)5]+[FeCl4]−,[21] which a platinum cathode reduces to polythiazyl.[22]

Uses

Due to its electrical conductivity, polythiazyl is used in LEDs, transistors, battery cathodes, and solar cells.[18]

Literature

King, R.S.P.: Novel chemistry and applications of polythiazyl, Doctoral Thesis Loughborough University 2009, pdf-Download

References

Template:Reflist

  1. ↑ a b Cite error: Invalid <ref> tag; no text was provided for refs named G&E
  2. ↑ a b c d Script error: No such module "Citation/CS1".
  3. ↑ Script error: No such module "Citation/CS1".
  4. ↑ Script error: No such module "citation/CS1".
  5. ↑ Script error: No such module "citation/CS1".
  6. ↑ Script error: No such module "Citation/CS1".
  7. ↑ Labes, M.M.; Love, P.; Nichols, L.F.: Polysulfur nitride - a metallic, superconducting polymer in Chem. Rev. 79 (1979) 1–15, Script error: No such module "doi"..
  8. ↑ a b c d Alsfasser, R.; Janiak, C.; Klapötke, T.M.; Meyer, H.-J.: Moderne Anorganische Chemie, Herausgeber Riedel, E., 3. Auflage 2007, Walter de Gruyter GmbH & Co. KG, Berlin/Boston, Template:ISBN, S. 129–132, (retrieved via De Gruyter Online).
  9. ↑ a b MacDiarmid, A.G.; Mikulski, C.M.; Saran, M.S.; Russo, P.J.; Cohen, M.J.; Bright, A.A.; Garito, A.F.; Heeger, A.J.: Synthesis and Selected Properties of Polymeric Sulfur Nitride, (Polythiazyl), (SN)x in Advances in Chemistry 150 (2009) 63–72, Script error: No such module "doi"..
  10. ↑ a b Template:RömppOnline
  11. ↑ Wiberg, E.; Wiberg, N.; Holleman, A.F.: Anorganische Chemie (in German), 103rd printing (2017) by Walter de Gruyter GmbH & Co. KG, Berlin/Boston, Template:ISBN, p. 681, (retrieved via De Gruyter Online).
  12. ↑ Baughman, R.H.; Apgar, P.A.; Chance, R.R.; MacDiarmid, A.G.; Garito, A.F.: A New Phase of (SN)x in J. Chem. Soc. Chem. Comm. 1977, 49–50, Script error: No such module "doi"..
  13. ↑ Script error: No such module "Citation/CS1".
  14. ↑ Script error: No such module "Citation/CS1".
  15. ↑ Script error: No such module "Citation/CS1".
  16. ↑ Boudeulle, M.: in Cryst. Struct. Comm. 4 (1975) 9–13.
  17. ↑ MacDiarmid, A.G.; Mikulski, C.M.; Russo, P.J.; Saran, M.S.; Garito, A.F.; Heeger, A.J.: Synthesis and structure of the polymeric metal, (SN)x, and its precursor, S2N2 in J. Chem. Soc. Chem. Comm. 1975, 476–477, Script error: No such module "doi"..
  18. ↑ a b Script error: No such module "citation/CS1".
  19. ↑ Script error: No such module "citation/CS1".
  20. ↑ Script error: No such module "citation/CS1".
  21. ↑ Script error: No such module "Citation/CS1".
  22. ↑ Script error: No such module "Citation/CS1".
Retrieved from "http://debianws.lexgopc.com/wiki143/index.php?title=Polythiazyl&oldid=2793891"