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Polycarbonyl

Polycarbonyl is a chemistry topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Polycarbonyl rather than just read about it. In short: Polycarbonyl, (also known as polymeric-CO, p-CO or poly-CO) is a solid, metastable, and explosive polymer of carbon monoxide. The polymer is produced by exposing carbon monoxide to high pressures.

Key takeaways

  • Polycarbonyl belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Polycarbonyl to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Polycarbonyl from memory before moving on to harder problems.

Reference excerpt

Polycarbonyl, (also known as polymeric-CO, p-CO or poly-CO) is a solid, metastable, and explosive polymer of carbon monoxide. 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.

Formation Poly-CO can be produced at pressures of 5.2 GPa; it is amorphous and yellow to dark red in color. Polymerisation is catalysed by blue light at slightly lower pressures in the δ-phase of solid CO. Another white, crystalline phase can be made at higher temperatures at 6 or 7 GPa. 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. 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. When exposed to the atmosphere it is hygroscopic, becomes gluey, and changes colour, becoming darker. The reaction with water produces carboxylic groups. The solid stores a high energy. It can decompose explosively forming glassy carbon and carbon dioxide. The energy density stored can be up to 8 kJ/g. During the decomposition the temperature can be 2500 K. The density is 1.65 g/cm3, however most of the solid produced is porous, so the true density is likely to be higher. 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. The 1600 is due to vibration of a C=C double bond. The solid is electrically insulating with an electronic gap energy of 1.9 eV. 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.

Structure Ideas of the structure include a zigzag chain of CO pointing in opposite directions, or five atom rings connected by CO and C−C bonds. The rings are lactones of tetronic acid: −C:−(C=O)−(C−O−)−(C=O)−O−. Interconnections between the rings are zigzags of CO. Other ideas of the structure of the solid, include graphitic carbon with carbon dioxide under pressure, and a polymer with this C3O2 monomer: −(C=O)−O−(C−)=C<. Yet other ideas are that the solid is the same as the polymer of carbon suboxide with oxalic anhydride.

References

Other reading Batyrev, I. G.; W. D. Mattson; B. M. Rice (2012). "Modeling of Early Stages of Formation of Poly-CO". MRS Proceedings. 1405 mrsf11-1405-y05-04. doi:10.1557/opl.2012.345. ISSN 1946-4274. Sun, Jian; Dennis D. Klug; Chris J. Pickard; Richard J. Needs (2011). "Controlling the Bonding and Band Gaps of Solid Carbon Monoxide with Pressure" (PDF). Physical Review Letters. 106 (14) 145502. Bibcode:2011PhRvL.106n5502S. doi:10.1103/PhysRevLett.106.145502. ISSN 0031-9007. PMID 21561202. S2CID 19591866.

Worked examples

Example 1 — a first encounter with Polycarbonyl

Start with the simplest possible case. Write down what Polycarbonyl claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Polycarbonyl before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Polycarbonyl ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Polycarbonyl

In research
Polycarbonyl appears in chemistry research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Polycarbonyl in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Polycarbonyl is common in secondary-school and first-year university syllabi. It links to neighbouring topics Explosive chemicals, Explosive polymers, Oxocarbons, so understanding it makes those chapters shorter.
In everyday life
Look for Polycarbonyl outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study Polycarbonyl in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Polycarbonyl means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Polycarbonyl out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Polycarbonyl in simple terms?

Polycarbonyl, (also known as polymeric-CO, p-CO or poly-CO) is a solid, metastable, and explosive polymer of carbon monoxide. The polymer is produced by exposing carbon monoxide to high pressures.

Why does Polycarbonyl matter?

Because it connects several chemistry ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Polycarbonyl?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Polycarbonyl.

Tags

  • Explosive chemicals
  • Explosive polymers
  • Oxocarbons

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