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Updated: May 27, 2025

Facile Preparation of 2Z,4E-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
New reactivity of late 3d transition metal complexes in catalytic reactions of alkynes
Shenghan Teng1, Peiyao Liang1, Jianrong Steve Zhou2
1Strait Institute of Flexible Electronics (SIFE, Future Technologies), Fujian Key Laboratory of Flexible Electronics, Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE), Fuzhou, 350117, China. ifeshhteng@fjnu.edu.cn.
Abstract:
Late 3d metals such as iron, cobalt, nickel, and copper are abundantly present in the Earth's crust and they are produced in huge quantities in the mining industry. Often, these inexpensive metals exhibit unique or special reactivities in catalytic reactions as compared with expensive noble metals such as palladium, iridium, and rhodium. The novel reactivities of 3d metal complexes originate from their unique physical and atomic properties as compared with heavier 4d/5d congeners: smaller ionic and covalent radii, contracted 3d orbitals of smaller sizes and lower energies, lower values of Pauli electronegativity, etc. This review summarizes the recent progress in late 3d transition metal-catalyzed transformations of alkynes. We organize catalytic examples according to each type of novel elementary reactivity exhibited by 3d metal complexes. Each section includes a description of the unique reactivity of the 3d metals, the atomic and theoretical basis of the reactivity and illustrations of catalytic examples: (1) single electron transfer from low-valent metal complexes to alkyl halides, (2) facile reductive elimination from nickel(III), (3) facile reductive elimination from copper(III), (4) cis-to-trans isomerization of alkenyl metal complexes after syn-insertion, (5) ligand-to-ligand hydrogen transfer, (6) hydrogen atom transfer from hydride complexes and (7) protonation of nickel metallacyclopropenes.
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Related Concept Videos
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Acidity of 1-Alkynes
The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Preparation of Alkynes: Alkylation Reaction
Alkylation of terminal alkynes with primary alkyl halides in the presence of a strong base like sodium amide is one of the common methods for the synthesis of longer carbon-chain alkynes. For example, treatment of 1-propyne with sodium amide followed by reaction with ethyl bromide yields 2-pentyne.
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.