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Polycarbonyl

From Wikipedia, the free encyclopedia
Polymer of carbon monoxide (CO)

Polycarbonyl, (also known aspolymeric-CO,p-CO orpoly-CO) is a solid,metastable, and explosivepolymer ofcarbon monoxide.[1] The polymer is produced by exposing carbon monoxide to high pressures. The structure of the solid appearsamorphous, but may include a zigzag of equally-spacedCO groups.[2]

Formation

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Poly-CO can be produced at pressures of 5.2 GPa; it isamorphous 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 carbideanvil in 1947. Originally this was thought to bepolymeric 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%.[6]

Properties

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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 formingglassy carbon andcarbon dioxide.[6] Theenergy 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 from13CO 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

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Ideas of the structure include a zigzag chain of CO pointing in opposite directions, or five atom rings connected by CO andC−C bonds. The rings arelactones oftetronic acid:−C:−(C=O)−(C−O)−(C=O)−O−. Interconnections between the rings are zigzags of CO.[4]

Other ideas of the structure of the solid, includegraphitic carbon with carbon dioxide under pressure, and a polymer with thisC3O2 monomer:−(C=O)−O−(C)=C<. Yet other ideas are that the solid is the same as the polymer ofcarbon suboxide withoxalic anhydride.[9]

References

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  1. ^abRademacher, N.; L. Bayarjargal; W. Morgenroth; B. Winkler; J. Ciezak-Jenkins (2011)."Preparation and characterization of solid carbon monoxide at high pressure in the diamond anvil cell"(PDF). Retrieved30 May 2013.
  2. ^Podeszwa, Rafał; Rodney J. Bartlett (2003). "Crystal orbital study of polycarbonyl".International Journal of Quantum Chemistry.95 (4–5):638–642.doi:10.1002/qua.10655.ISSN 0020-7608.
  3. ^Rademacher, Nadine; Lkhamsuren Bayarjargal; Wolfgang Morgenroth; Jennifer Ciezak-Jenkins; Sasha Batyrev; Björn Winkler."High Pressure Investigations of Liquid and Polymerized CO up to 20 GPa Using Pair Distribution Function Analysis"(PDF). Retrieved30 May 2013.
  4. ^abcdBernard, Stephane (Feb 1998)."DECOMPOSITION AND POLYMERIZATION OF SOLID CARBON MONOXIDE UNDER PRESSURE"(PDF). Trieste. Retrieved30 May 2013.
  5. ^abMills, R. L.; D. Schiferl; A. I. Katz; B. W. Olinger (1984)."New Phases and Chemical Reactions in Solid Co Under Pressure"(PDF).Le Journal de Physique Colloques.45 (C8): C8–187–C8–190.doi:10.1051/jphyscol:1984833.ISSN 0449-1947.
  6. ^abcdefgLipp, Magnus J.; William J. Evans, Bruce J. Baer, Choong-Shik Yoo; Baer, Bruce J.; Yoo, Choong-Shik (2005)."High-energy-density extended CO solid"(PDF).Nature Materials.4 (3):211–215.Bibcode:2005NatMa...4..211L.doi:10.1038/nmat1321.ISSN 1476-1122.PMID 15711555.S2CID 25779399.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  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.doi:10.1021/jp900586a.ISSN 1520-6106.PMID 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.doi:10.1021/j150659a007.ISSN 0022-3654.
  9. ^Lipp, M.; W. J. Evans; V. Garcia-Baonza; H. E. Lorenzana (1998). "Carbon Monoxide: Spectroscopic Characterization of the High–Pressure Polymerized Phase".Journal of Low Temperature Physics.111 (3/4):247–256.Bibcode:1998JLTP..111..247L.doi:10.1023/A:1022267115640.ISSN 0022-2291.S2CID 116687814.

Other reading

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Common oxides
Exotic oxides
Polymers
Compounds derived from oxides
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