Related Experiment Video
Updated: Jun 17, 2026

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
A Cu8Na2-silsesquioxane/acetylacetonate precatalyst for the one-pot cyclohexane to ε-caprolactone transformation
Zhibin Huang1, Victor N Khrustalev1,2, Elena S Shubina3
1Peoples' Friendship University of Russia (RUDN University), Miklukho-Maklaya St. 6, 117198, Moscow, Russian Federation. bilyachenko@ineos.ac.ru.
Abstract:
Self-assembly of heterometallic (copper/sodium) complexes stabilized by phenylsiloxanolate and acetylacetonate ligands resulted in Cu8Na2-cage structures. Their unprecedented cage-like geometry features two peripheral Cu3 and one central Na-Cu2-Na linear fragments surrounded by two Si5-cyclic silsesquioxanes and four acetylacetonate ligands. To evaluate its catalytic performance, the Cu8Na2-precatalyst was explored in the oxidation of cyclohexane, selected as a model substrate, under a range of experimental conditions. The best results were obtained at 80 °C for 0.5 h under MW irradiation, affording ε-caprolactone (TON = 145, TOF = 290 h-1) along with cyclohexanol and cyclohexanone, in an overall yield of 15%. These promising preliminary findings highlight the potential of the heterometallic Cu8Na2 system as an efficient and selective precatalyst for rapid MW-assisted single-pot oxidation, under mild conditions, of cyclohexane to ε-caprolactone, a compound with a marked industrial interest.
More Related Videos
10:17Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
11:42Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
Related Concept Videos
Cycloaddition Reactions: Overview
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement