Related Experiment Video
Updated: Mar 18, 2026

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Rational design of a polyphenyl octacarboxylate HOF for highly selective separation of benzene over cyclohexane
Biying Liu1, Ying Wang2, Miao She1
1School of Environmental and Chemical Engineering, Foshan University Foshan 528000 P. R. China huangliyun@fosu.edu.cn hnyuanwb@126.com.
Abstract:
The separation of benzene and cyclohexane is a long-standing challenge in the petrochemical industry, yet conventional distillation remains highly energy-intensive due to the nearly identical boiling points of the two molecules. Adsorptive separation offers a far more energy-efficient alternative; however, the development of adsorbents that simultaneously combine stable lightweight structures, high adsorption capacity, and strong selectivity remains difficult. To overcome these limitations, we present a robust hydrogen-bonded organic framework, H8ETTOB-HOF, constructed from a polyphenyl octacarboxylic acid linker. Its precisely engineered pore architecture and tailored electrostatic environment work synergistically to enhance benzene affinity, affording exceptional benzene/cyclohexane selectivity (16.9) and a high adsorption capacity (3.9 mmol g-1 at 298 K, 13 kPa), surpassing all previously reported HOFs. Density functional theory shows that the synergistic C-H⋯O and C-H⋯π interactions facilitate benzene capture. Experimental investigations employing dynamic columns demonstrate efficient one-step benzene purification from equimolar mixtures, showcasing excellent recyclability. This work highlights a strategic approach to constructing stable, multifunctional HOFs for challenging hydrocarbon separations.
More Related Videos
05:34Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes
Published on: December 16, 2019
09:08Separation of Aldehydes and Reactive Ketones from Mixtures Using a Bisulfite Extraction Protocol
Published on: April 2, 2018
Related Concept Videos
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
Frost Circles for Different Conjugated Systems
Benzene to Phenol via Cumene: Hock Process
Hydrolysis of Chlorobenzene to Phenol: Dow Process