Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride01:26

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride

1.9K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
1.9K
Thermal Electrocyclic Reactions: Stereochemistry01:17

Thermal Electrocyclic Reactions: Stereochemistry

2.1K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
2.1K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Synergistic Pore Microenvironment Engineering in Zinc Metal-Organic Frameworks for High SF<sub>6</sub>/N<sub>2</sub> Selectivity and Humidity-Resistant Trace SF<sub>6</sub> Capture.

Angewandte Chemie (International ed. in English)·2026
Same author

Bent ligand-directed assembly and adsorption property modulation of pseudo-tetrahedral polyoxometalate-organic cages.

Chemical communications (Cambridge, England)·2026
Same author

Amino Functionalization-Induced Coordination Geometry Switch Enables Pore Size Exclusion and Selective CHF<sub>3</sub> Capture in Two Cu-Based Metal-Organic Frameworks.

Inorganic chemistry·2026
Same author

A Robust Metal-Organic Framework With 'Molecular Gates' for Efficient Separation of Ethane From Ethylene.

Angewandte Chemie (International ed. in English)·2026
Same author

Efficient one-step SO<sub>2</sub> capture from industrial flue gas <i>via</i> a scalable Zr-based metal-organic framework.

Dalton transactions (Cambridge, England : 2003)·2026
Same author

DMF-Mediated Diffusion Regulation in Pyridine-Carboxylate Metal-Organic Frameworks Enables Efficient CHF<sub>3</sub> Capture.

Angewandte Chemie (International ed. in English)·2026

Related Experiment Video

Updated: Sep 9, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

3.4K

Selective Toluene Separation via π-π Interactions in Cobalt sql Network Rubber Composites.

Guo-Bi Li1, Jing Chen1, Bai-Qiao Song2

  • 1School of Chemistry and Chemical Engineering, Lingnan Normal University, Zhanjiang 524048, P.R. China.

ACS Applied Materials & Interfaces
|September 2, 2025
PubMed
Summary

A new hybrid membrane effectively removes toluene, a common aromatic contaminant, from water using selective molecular recognition. This advanced material offers high purity and recovery for environmental remediation.

Keywords:
composite filmscoordination networksnaphthalene diimidetoluene extractionwater remediation

More Related Videos

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols
10:12

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols

Published on: April 4, 2014

13.1K
1,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions
06:56

1,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions

Published on: October 10, 2016

7.8K

Related Experiment Videos

Last Updated: Sep 9, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

3.4K
Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols
10:12

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols

Published on: April 4, 2014

13.1K
1,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions
06:56

1,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions

Published on: October 10, 2016

7.8K

Area of Science:

  • Materials Science
  • Environmental Chemistry
  • Nanotechnology

Background:

  • Aromatic contaminants in water pose environmental challenges.
  • Developing materials for selective contaminant removal is crucial for remediation.

Purpose of the Study:

  • To design and characterize a framework-elastomer hybrid membrane for selective toluene recovery.
  • To investigate the molecular recognition mechanisms for toluene separation.

Main Methods:

  • Fabrication of a hybrid membrane with [Co(4-pmntd)2(NO3)2] (4-pmntd = N,N'-bis(4-pyridylmethyl)naphthalene diimide).
  • Structural analysis using crystallographic diffraction, gas adsorption, spectroscopy, and NMR.
  • Computational modeling with GCMC and DFT-D to study sorption pathways.

Main Results:

  • The membrane demonstrated high selectivity for toluene via π-π charge-transfer interactions.
  • Achieved toluene detection at 5.3 × 10⁻⁶ mol/L with 97.6% purity and 94.0% recovery.
  • The material showed rapid kinetics, ambient temperature operation, and excellent recyclability.

Conclusions:

  • The developed hybrid membrane is a sustainable solution for industrial toluene remediation.
  • Advances coordination-network-based separation technology for environmental water treatment.
  • Confirms selective molecular recognition mechanism through computational and experimental validation.