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

Electrolysis03:00

Electrolysis

26.6K
In a galvanic cell, the electrical work is done by a redox system on its surroundings as electrons produced by the spontaneous redox reactions are transferred through an external circuit. Alternatively, an external circuit does work on a redox system by imposing a voltage sufficient to drive an otherwise nonspontaneous reaction in a process known as electrolysis. For instance, recharging a battery involves the use of an external power source to drive the spontaneous (discharge) cell reaction in...
26.6K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

3.4K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
3.4K
E1 Reaction: Kinetics and Mechanism02:46

E1 Reaction: Kinetics and Mechanism

15.6K
Here, in contrast to the E2 reaction mechanism, we delve into the aspects of the E1 reaction mechanism, which has two steps: rate-limiting loss of the leaving group and abstraction of the beta hydrogen by a weak base. Typically, the experimental proof for the E1 mechanism is via kinetic studies or isotope studies. While the former demonstrates the first-order kinetics—the dependence of the reaction solely on substrate concentration—the latter proves the abstraction of hydrogen only...
15.6K
E2 Reaction: Kinetics and Mechanism02:45

E2 Reaction: Kinetics and Mechanism

10.4K
SN2 substitutions and E2 eliminations of alkyl halides proceed via a concerted pathway. While the nucleophile attacks the alpha carbon in SN2 reactions, it functions as a strong base and abstracts a beta hydrogen in the E2 mechanism. The rate-limiting transition state in E2 elimination reactions is characterized by partially broken carbon–hydrogen and carbon–halogen bonds and a partially formed pi bond between the alpha and beta carbons. The beta hydrogen and halide are eliminated...
10.4K
Metabolism of Chemolithotrophs01:15

Metabolism of Chemolithotrophs

40
Chemolithotrophs are microorganisms that obtain energy by oxidizing inorganic molecules such as hydrogen gas (H₂), ammonia (NH₃), reduced sulfur compounds (H₂S, S²⁻), and ferrous iron (Fe²⁺). Unlike heterotrophic organisms that rely on organic carbon, chemolithotrophs transfer electrons from these inorganic donors to the electron transport chain (ETC), generating a proton motive force (PMF) that drives ATP synthesis through oxidative phosphorylation.
40
Acid Halides to Carboxylic Acids: Hydrolysis01:01

Acid Halides to Carboxylic Acids: Hydrolysis

2.7K
Hydrolysis of acid halides is a nucleophilic acyl substitution reaction in which acid halides react with water to give carboxylic acids. The reaction occurs readily and does not require acid or a base catalyst.
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
2.7K

You might also read

Related Articles

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

Sort by
Same author

Rethinking Bloom-Risk Management in Recovering Shallow Lakes: From Visible Surface Events to Latent Risk.

Environmental science & technology·2026
Same author

Electrochemical Generation of Nonradical Hydrotrioxide for Sustainable Water Purification.

Environmental science & technology·2026
Same author

Boosting Photocatalytic Overall Water Splitting Activity of Phosphorene Through Five-Coordinate Passivation Enabled by Carbene Addition.

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

Profiling Active Low-Abundance Microbes in As/Sb-Contaminated Soils via d-Amino Acid-Based In Situ Labeling.

Environmental science & technology·2026
Same author

Function-Oriented and Waste-Derived Single-Atom Catalysts for Water Purification.

Chemical reviews·2026
Same author

Sb-Enabled Dimensional Reprogramming of Palladium Nanoclusters for Enhanced Catalysis.

Advanced materials (Deerfield Beach, Fla.)·2026

Related Experiment Video

Updated: Jul 18, 2025

Characterizing Electron Transport through Living Biofilms
08:52

Characterizing Electron Transport through Living Biofilms

Published on: June 1, 2018

8.5K

Mimicking reductive dehalogenases for efficient electrocatalytic water dechlorination.

Yuan Min1, Shu-Chuan Mei1, Xiao-Qiang Pan1

  • 1Department of Environmental Science and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, China.

Nature Communications
|August 23, 2023
PubMed
Summary

Researchers developed a novel electrocatalyst by mimicking natural enzymes to efficiently remove chlorinated pollutants from water. This biomimetic approach enhances dechlorination activity and selectivity for cleaner water treatment.

More Related Videos

Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1
09:00

Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1

Published on: April 16, 2018

10.1K
Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
10:21

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions

Published on: October 5, 2019

8.4K

Related Experiment Videos

Last Updated: Jul 18, 2025

Characterizing Electron Transport through Living Biofilms
08:52

Characterizing Electron Transport through Living Biofilms

Published on: June 1, 2018

8.5K
Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1
09:00

Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1

Published on: April 16, 2018

10.1K
Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
10:21

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions

Published on: October 5, 2019

8.4K

Area of Science:

  • Environmental Chemistry
  • Materials Science
  • Biotechnology

Background:

  • Electrochemical technology offers a promising route for degrading persistent chlorinated organic pollutants in water.
  • Designing electrocatalysts with high activity and selectivity comparable to natural enzymes remains a significant challenge.

Purpose of the Study:

  • To design high-performance electrocatalysts for water dechlorination by mimicking the structure and function of natural reductive dehalogenases.
  • To investigate the role of a specific structural configuration in enhancing catalytic efficiency.

Main Methods:

  • Assembled a heterostructure electrocatalyst by sandwiching a molecular catalyst within two-dimensional graphene oxide interlayers.
  • Evaluated the electrocatalyst's performance in water dechlorination, focusing on the reduction of dichloroacetic acid.
  • Utilized molecular simulations to understand the mechanism of action and the role of the sandwiched structure.

Main Results:

  • The designed electrocatalyst demonstrated excellent dechlorination performance.
  • The sandwiched configuration enhanced the reduction of dichloroacetic acid by 7.8-fold compared to non-sandwiched structures.
  • The catalyst selectively converted trichloro-groups to monochloro-groups, indicating high selectivity.
  • Molecular simulations revealed the importance of the inner sandwiched space in tuning solvation, protonation, and facilitating C-Cl bond cleavage.

Conclusions:

  • Mimicking natural reductive dehalogenases is a viable strategy for developing efficient electrocatalysts for water treatment.
  • The designed heterostructure electrocatalyst shows significant potential for the sustainable remediation of organohalogen-contaminated water and wastewater.