In organometallic chemistry, acetylide refers to chemical compounds with the chemical formulas MC≡CH and MC≡CM, where M is a metal.^[1] The term is used loosely and can refer to substituted acetylides having the general structure RC≡CM (where R is an organic side chain). Acetylides are reagents in organic synthesis. The calcium acetylide commonly called calcium carbide is a major compound of commerce.

Structure and bonding

Structure of the cluster formed from PhC₂Li complexed to N,N,N′,N′-tetramethyl-1,6-diaminohexane (methylene groups omitted for clarity). Color key: turquoise = Li, blue = N.^[2]

Structure of Na₂C₂.^[3] Color code: gray = C, blue = Na.

Alkali metal and alkaline earth metal acetylides of the general formula MC≡CM are salt-like Zintl phase compounds, containing C²⁻
₂ ions. Evidence for this ionic character can be seen in the ready hydrolysis of these compounds to form acetylene and metal oxides, there is also some evidence for the solubility of C²⁻
₂ ions in liquid ammonia.^[4] The C²⁻
₂ ion has a closed shell ground state of ¹Σ⁺
_g, making it isoelectronic to a neutral molecule N₂,^[5] which may afford it some stability.

Analogous acetylides prepared from other metals, particularly transition metals, show covalent character and are invariably associated with their metal centers. This can be seen in their general stability to water (such as silver acetylide, copper acetylide) and radically different chemical applications.

Acetylides of the general formula RC≡CM (where R = H or alkyl) generally show similar properties to their doubly substituted analogues. In the absence of additional ligands, metal acetylides adopt polymeric structures wherein the acetylide groups are bridging ligands.

Portion of the structure of the polymer copper phenylacetylide (CuC₂C₆H₅).^[6]

Preparation

Terminal alkynes are weak acids:^[7]

RC≡CH + R″M ⇌ R″H + RC≡CM

To generate acetylides from acetylene and alkynes relies on the use of organometallic^[8] or inorganic^[9] superbases in solvents which are less acidic than the terminal alkyne. In early studies liquid ammonia was employed, but ethereal solvents are more common.

Lithium amide,^[7] LiHMDS,^[10] or organolithium reagents, such as butyllithium,^[8] are frequently used to form lithium acetylides:

${\displaystyle {\ce {{H-C{\equiv }C-H}+{\overset {butyllithium}{BuLi}}->[{\ce {THF}}][-78^{\circ }{\ce {C}}]{Li-\!{\equiv }\!-H}+BuH}}}$

Monopotassium and monosodium acetylide can be prepared from various inorganic reagents (such as sodium amide)^[9] or from their elemental metals, often at room temperature and atmospheric pressure.^[7]

Copper(I) acetylide can be prepared by passing acetylene through an aqueous solution of copper(I) chloride because of a low solubility equilibrium.^[7] Similarly, silver acetylides can be obtained from silver nitrate.

Calcium carbide is prepared by heating carbon with lime (calcium oxide) at approximately 2,000 °C. A similar process is used to produce lithium carbide.

Reactions

Acetylides of the type RC₂M are widely used in alkynylations in organic chemistry. They are nucleophiles that add to a variety of electrophilic and unsaturated substrates. A classic application is the Favorskii reaction.

Illustrative is the sequence shown below, ethyl propiolate is deprotonated by n-butyllithium to give the corresponding acetylide. This acetylide adds to the carbonyl center of cyclopentanone. Hydrolytic workup liberate the alkynyl alcohol.^[11]

Reaction of ethyl propiolate with n-butyllithium to form the lithium acetylide.

Hazards

Some acetylides are notoriously explosive.^[12] Formation of acetylides poses a risk in handling of gaseous acetylene in presence of metals such as mercury, silver or copper, or alloys with their high content (brass, bronze, silver solder).

See also

• Ethynyl
• Ethynyl radical
• Diatomic carbon (neutral C₂)
• Acetylenediol

References