Polycarbonyl Explained

Polycarbonyl, (also known as polymeric-CO, p-CO or poly-CO) is a solid, metastable, and explosive polymer of carbon monoxide.[1] The polymer is produced by exposing carbon monoxide to high pressures. The structure of the solid appears amorphous, but may include a zigzag of equally-spaced CO groups.[2]

Formation

Poly-CO can be produced at pressures of 5.2 GPa; it is amorphous and yellow to dark red in color.[3] Polymerisation is catalysed by blue light at slightly lower pressures in the δ-phase of solid CO.[4] Another white, crystalline phase can be made at higher temperatures at 6 or 7 GPa.[1]

R. J. Mills discovered this solid, which was first produced in a tungsten carbide anvil in 1947. Originally this was thought to be polymeric carbon suboxide, but the formation does not yield any gas byproduct such as carbon dioxide.[5] The yield of the solid can be up to 95%.

Properties

The polymer is stable above about 80 K. Below this temperature the ε form of solid molecular CO is formed instead. When the pressure is released the polymer remains stable at atmospheric pressure. The solid dissolves in water, alcohol and acetone.[5] When exposed to the atmosphere it is hygroscopic, becomes gluey, and changes colour, becoming darker.[6] The reaction with water produces carboxylic groups.[7] [8]

The solid stores a high energy. It can decompose explosively forming glassy carbon and carbon dioxide.[6] The energy density stored can be up to 8 kJ/g. During the decomposition the temperature can be 2500 K.[6] The density is 1.65 g/cm3, however most of the solid produced is porous, so the true density is likely to be higher.[6]

Infrared spectroscopy shows bands at 650, 1210, 1440, 1650 and 1760 cm−1. The 1760 band is likely to be due to the -C-(C=O)-C- structure.[4] The 1600 is due to vibration of a C=C double bond.[6]

The solid is electrically insulating with an electronic gap energy of 1.9 eV.[4]

Nuclear magnetic resonance for the material made from 13CO shows sharp resonance at 223 ppm due to ester or lactone attached carbon, and 151 ppm due to C=C double bonds. There is also broad resonance at 109 and 189 ppm. Over time of a few days, the 223 ppm peak reduces and all the other features increase in strength.[6]

Structure

Ideas of the structure include a zigzag chain of CO pointing in opposite directions, or five atom rings connected by CO and bonds. The rings are lactones of tetronic acid: . Interconnections between the rings are zigzags of CO.[4]

Other ideas of the structure of the solid, include graphitic carbon with carbon dioxide under pressure, and a polymer with this monomer: . Yet other ideas are that the solid is the same as the polymer of carbon suboxide with oxalic anhydride.[9]

References

  1. Web site: Preparation and characterization of solid carbon monoxide at high pressure in the diamond anvil cell. Rademacher. N.. L. Bayarjargal . W. Morgenroth . B. Winkler . J. Ciezak-Jenkins . 2011. 30 May 2013.
  2. Podeszwa. Rafał. Rodney J. Bartlett. 2003. Crystal orbital study of polycarbonyl. International Journal of Quantum Chemistry. 95. 4–5. 638–642. 0020-7608. 10.1002/qua.10655.
  3. Web site: High Pressure Investigations of Liquid and Polymerized CO up to 20 GPa Using Pair Distribution Function Analysis. Rademacher. Nadine. Lkhamsuren Bayarjargal . Wolfgang Morgenroth . Jennifer Ciezak-Jenkins . Sasha Batyrev . Björn Winkler . 30 May 2013.
  4. Web site: DECOMPOSITION AND POLYMERIZATION OF SOLID CARBON MONOXIDE UNDER PRESSURE. Bernard. Stephane. Feb 1998. 30 May 2013. Trieste.
  5. Mills. R. L.. D. Schiferl . A. I. Katz . B. W. Olinger . New Phases and Chemical Reactions in Solid Co Under Pressure. 1984. Le Journal de Physique Colloques. 45. C8. C8–187–C8–190. 0449-1947. 10.1051/jphyscol:1984833.
  6. Lipp. Magnus J.. William J. Evans, Bruce J. Baer, Choong-Shik Yoo. 2005. High-energy-density extended CO solid. Nature Materials. 4. 3. 211–215. 1476-1122. 10.1038/nmat1321. 15711555. 2005NatMa...4..211L. Baer. Bruce J.. Yoo. Choong-Shik. 25779399.
  7. Ceppatelli. Matteo. Anton Serdyukov . Roberto Bini . Hans J. Jodl . 2009. Pressure Induced Reactivity of Solid CO by FTIR Studies. The Journal of Physical Chemistry B. 113. 19. 6652–6660. 1520-6106. 10.1021/jp900586a. 19368397.
  8. Katz. Allen I.. David Schiferl . Robert L. Mills . 1984. New phases and chemical reactions in solid carbon monoxide under pressure. The Journal of Physical Chemistry. 88. 15. 3176–3179. 0022-3654. 10.1021/j150659a007.
  9. Lipp. M.. W. J. Evans . V. Garcia-Baonza . H. E. Lorenzana . 1998. Journal of Low Temperature Physics. 111. 3/4. 247–256. 0022-2291. 10.1023/A:1022267115640. Carbon Monoxide: Spectroscopic Characterization of the High–Pressure Polymerized Phase. 1998JLTP..111..247L. 116687814.

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