Air-free technique

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Air-free techniques refer to a range of manipulations in the chemistry laboratory for the handling of compounds that are air-sensitive. These techniques prevent the compounds from reacting with components of air, usually water and oxygen; less commonly carbon dioxide and nitrogen. A common theme among these techniques is the use of a high vacuum to remove air, and the use of an inert gas: preferably argon, but often nitrogen.

The two most common types of air-free technique involve the use of a glovebox and a Schlenk line. In both methods, glassware (often Schlenk tubes) are pre-dried in ovens prior to use. They may be flame-dried to remove adsorbed water. Prior to coming into an inert atmosphere, vessels are further dried by purge-and-refill — the vessel is subjected to a vacuum to remove gases and water, and then refilled with inert gas. This cycle is usually repeated three times or the vacuum is applied for an extend period of time. One of the differences between the use of a glovebox and a Schlenk line is where the purge-and-refill cycle is applied. When using a glovebox the purge-and-refill is applied to an airlock attached to the glovebox, commonly called the "port" or "ante-chamber". In contrast when using a Schlenk line the purge-and-refill is applied directly to the reaction vessel through a hose or ground glass joint that is connected to the manifold.[1]

Contents

[edit] Glovebox

An ordinary glovebox, showing the two gloves for manipulation, with airlock on the right.
An ordinary glovebox, showing the two gloves for manipulation, with airlock on the right.

The most straightforward type of air-free technique is the use of a glovebox. A glove bag uses the same idea, but is usually a poorer substitute because it is more difficult to purge, and less well sealed.

Normal laboratory equipment can be set up and manipulated through the use of the gloves. By providing a sealed but recirculating atmosphere of the inert gas, few other precautions are necessary. Inventive ways of accessing items beyond the reach of the gloves exist, such as the use of tongs and strings. The main drawbacks to using a glovebox are the cost of the glovebox itself, and limited dexterity wearing the gloves. Cross contamination of samples due to poor technique is also acute, especially where a glovebox is shared.

Because gloveboxes are expensive and have limited space, it is common for gloveboxes to be used to store, weigh, and transfer air-sensitive chemicals. Reactions are thereafter carried out using Schlenk technique. The gloveboxes are thus only used for the most air-sensitive reactions.

[edit] Schlenk line

A Schlenk line with four ports.
A Schlenk line with four ports.

The other main types of techniques are associated with the use of a Schlenk line. The main methods here are:

  • counterflow additions, where air-stable reagents are added to the reaction vessel against a flow of inert gas.
  • the use of rubber septa with syringes to transfer liquids and solutions
  • cannula transfer, where liquids or solutions of air-sensitive reagents are transferred between different vessels stoppered with septa using cannulae. Liquid flow is achieved via vacuum or inert gas pressure.[2]
    A cannula is used to transfer THF from the flask on the right to the flask on the left.
    A cannula is used to transfer THF from the flask on the right to the flask on the left.

Glassware are usually connected via tightly-fitting and greased ground glass joints. Round bends of glass tubing with ground glass joints may be used to adjust the orientation of various vessels.

Filtration under inert conditions poses a special challenge which is usually tackled with specialized glassware. A Schlenk filter consists of sintered glass funnel fitted with joints and stopcocks. By fitting the pre-dried funnel and receiving flask to the reaction flask against a flow of nitrogen, carefully inverting the set-up, and turning on the vacuum appropriately, the filtration may be accomplished with minimal exposure to air.

[edit] Other air-free methods

  • air-free distillation - e.g. see reflux still, Perkin triangle
  • air-free filtration - e.g. see filter stick (see gallery below), swivel frit
  • air-free sublimation - see gallery below for a drawing scheme for an example
  • air-free solid addition - e.g. see solid addition tube, swivel frit
  • air-free liquid addition - e.g. see cannulation, syringing, dropping funnel, vacuum transfer
  • air-free NMR tube preparation

[edit] Associated preparations

Commercially available purified inert gas (argon or nitrogen) is adequate for most purposes. However, for certain applications, it is necessary to further remove water and oxygen. This additional purification can be accomplished by piping the inert gas line through a heated column of copper catalyst, which converts the oxygen to copper oxide. Water is removed by piping the gas through a column of desiccant such as phosphorus pentoxide or molecular sieves.

Air- and water-free solvents are also necessary. If high-purity solvents are available in nitrogen-purged Winchesters, they can be brought directly into the glovebox. For use with Schlenk technique, they can be quickly poured into Schlenk flasks charged with molecular sieves, and degassed. More typically, solvent is dispensed directly from a still or solvent purification column.

[edit] Degassing

See also: degasification

Two procedures for degassing are common. The first is known as freeze-pump-thaw — the solvent is frozen under liquid nitrogen, and a vacuum is applied. Thereafter, the stopcock is closed and the solvent is thawed in warm water, allowing trapped bubbles of gas escape.[3]

The second procedure is to simply subject the solvent to a vacuum. Stirring or mechanical agitation using a ultrasonicator is useful. Dissolved gases evolve first; once the solvent starts to evaporate, noted by condensation outside the flask walls, the flask is refilled with inert gas. Both procedures are repeated three times.

[edit] Drying

After being refluxed with sodium and benzophenone to remove oxygen and water, toluene is distilled under inert gas into a receiving flask.
After being refluxed with sodium and benzophenone to remove oxygen and water, toluene is distilled under inert gas into a receiving flask.

Solvent are traditionally purified by distillation over an appropriate desiccant under an inert atmosphere. The main problem with the use of sodium as a desiccant (below its melting point) is associated with the slow rate of reaction between a solid and a solution. When however, the desiccant is soluble, the speed of drying is much higher. Benzophenone is often used to generate such a soluble drying agent. An advantage to this application is the intense blue color of the ketyl radical anion. Thus, sodium/benzophenone can be used as an indicator of air-free and moisture-free conditions in the purification of solvents by distillation.[4][5]

However, distillation stills are fire hazards and are increasingly being replaced by alternative solvent-drying systems. Particularly popular is the filtration of deoxygenated solvents through columns filled with activated alumina.[6]

Drying of solids can be brought about by storing the solid over a drying agent such as P2O5 or silica, storing in a drying oven/vacuum-drying oven, heating under a high vacuum or in a drying pistol, or to remove trace amounts of water, simply storing the solid in a glove box that has a dry atmosphere.

[edit] Alternatives

Both these techniques require rather expensive equipment. Where air-free requirements are not as stringent, other techniques exist. For example, for preparing Grignard reagents which hydrolyze on exposure to water, it is usually sufficient to connect a guard tube filled with calcium chloride to the reflux condenser to prevent moisture contamination.

In situ desiccants such as molecular sieves, or the removal of water by azeotropic distillation can also be used.

[edit] References

  1. ^ Duward F. Shriver and M. A. Drezdzon "The Manipulation of Air-Sensitive Compounds" 1986, J. Wiley and Sons: New York. ISBN 0-471-86773-X.
  2. ^ Brown, H. C. “Organic Syntheses via Boranes” John Wiley & Sons, Inc. New York: 1975. ISBN 0-471-11280-1.
  3. ^ Mark Lonergan. Freeze-Pump-Thaw Degassing of Liquids. University of Oregon.
  4. ^ Nathan L. Bauld (2001). Unit 6: Anion Radicals. University of Texas.
  5. ^ W. L. F. Armarego and C. Chai (2003). Purification of laboratory chemicals. Butterworth-Heinemann. ISBN 0750675713. 
  6. ^ Pangborn, A. B.; Giardello, M. A.; Grubbs, R. H.; Rosen, R. K. and Timmers, F. J. (1996). "Safe and Convenient Procedure for Solvent Purification". Organometallics 15 (5): 1518-20. doi:10.1021/om9503712. 

[edit] See also

[edit] External links


[edit] Gallery

Perkin_triangle: Air-sensitive distillations

Air-free filtration

Air-free sublimation

Cannula: intra-bleed valve

Cannula: extra-bleed valve

Cannula: (Simple) no bleed valve

Cannula: two manifold system

Cannula: syringe valve

Teflon tap for air-sensitive NMR samples