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

Ion Exchange01:17

Ion Exchange

547
Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
547
Ion-Exchange Chromatography01:09

Ion-Exchange Chromatography

358
Ion-exchange chromatography, or IEC, is a technique for separating ions based on their affinity for the stationary phase. The stationary phase is a cross-linked polymer resin with covalently attached ionic functional groups. The functional groups can be either positively charged (cation exchangers) or negatively charged (anion exchangers). A cation exchanger consists of a polymeric anion and active cations, while an anion exchanger is a polymeric cation with active anions. The choice of...
358
Aqueous Solutions and Heats of Hydration02:42

Aqueous Solutions and Heats of Hydration

14.4K
Water and other polar molecules are attracted to ions. The electrostatic attraction between an ion and a molecule with a dipole is called an ion-dipole attraction. These attractions play an important role in the dissolution of ionic compounds in water.
When ionic compounds dissolve in water, the ions in the solid separate and disperse uniformly throughout the solution because water molecules surround and solvate the ions, reducing the strong electrostatic forces between them. This process...
14.4K
Extraction: Advanced Methods00:56

Extraction: Advanced Methods

415
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
415
Potentiometry: Membrane Electrodes01:15

Potentiometry: Membrane Electrodes

458
Membrane electrodes, also known as p-ion electrodes, use membranes that selectively interact with free analyte ions, generating a potential difference across the membrane. The resulting membrane potential, known as the asymmetry potential, is not zero even when analyte concentrations on both sides of the membrane are equal. The membrane's response is typically not selective to a single analyte but proportional to the concentration of all ions in the sample solution capable of interacting at...
458
Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule02:17

Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule

13.9K
If a set of reactants can yield multiple constitutional isomers, but one of the isomers is obtained as the major product, the reaction is said to be regioselective. In such reactions, bond formation or breaking is favored at one reaction site over others.
The hydrohalogenation of an unsymmetrical alkene can yield two haloalkane products, depending on which vinylic carbon takes up the halogen. However, one product usually predominates, where hydrogen adds to the vinylic carbon bearing the...
13.9K

You might also read

Related Articles

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

Sort by
Same author

Spontaneous Isomerization of Tau is Most Prevalent in Alzheimer's Disease.

NeuroMarkers·2026
Same author

Predicting Recurrence Risk of Glioblastoma Based on Preoperative-Postoperative Longitudinal MRI: A Multicenter Study.

Bioengineering (Basel, Switzerland)·2026
Same author

Remediating Biotoxicity with Synthetic Receptors.

ACS central science·2026
Same author

Tolvaptan for hyponatremia in patients with cirrhosis: a post hoc subgroup analysis of a multicenter, randomized, double-blind, placebo-controlled trial.

Hepatology international·2026
Same author

Cationic imidazolium macrocycles enable array-based, site-selective optical detection of peptide phosphorylation.

Organic & biomolecular chemistry·2026
Same author

Unique Pathways that drive CD8+ T cell dysfunction and immune evasion in lung adenocarcinoma.

American journal of respiratory cell and molecular biology·2026

Related Experiment Video

Updated: Jun 5, 2025

Sulfate Separation by Selective Crystallization with a Bis-iminoguanidinium Ligand
08:01

Sulfate Separation by Selective Crystallization with a Bis-iminoguanidinium Ligand

Published on: September 8, 2016

8.4K

Selective aqueous anion recognition in an anionic host.

Noa Bar Ziv1, Chengwei Chen1, Bryce da Camara1

  • 1Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA 92521, USA.

Iscience
|December 6, 2024
PubMed
Summary
This summary is machine-generated.

Water-soluble iron cages (Fe4L44-) can encapsulate specific anions like hexafluorophosphate (PF6-) in aqueous solutions. These anionic cages exhibit slow anion exchange, offering potential for controlled environmental anion release applications.

Keywords:
ChemistrySupramolecular chemistry

More Related Videos

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
10:39

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction

Published on: August 23, 2018

7.8K
Selection of Transporter-Targeted Inhibitory Nanobodies by Solid-Supported-Membrane SSM-Based Electrophysiology
09:12

Selection of Transporter-Targeted Inhibitory Nanobodies by Solid-Supported-Membrane SSM-Based Electrophysiology

Published on: May 3, 2021

2.5K

Related Experiment Videos

Last Updated: Jun 5, 2025

Sulfate Separation by Selective Crystallization with a Bis-iminoguanidinium Ligand
08:01

Sulfate Separation by Selective Crystallization with a Bis-iminoguanidinium Ligand

Published on: September 8, 2016

8.4K
Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
10:39

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction

Published on: August 23, 2018

7.8K
Selection of Transporter-Targeted Inhibitory Nanobodies by Solid-Supported-Membrane SSM-Based Electrophysiology
09:12

Selection of Transporter-Targeted Inhibitory Nanobodies by Solid-Supported-Membrane SSM-Based Electrophysiology

Published on: May 3, 2021

2.5K

Area of Science:

  • Supramolecular Chemistry
  • Coordination Chemistry
  • Materials Science

Background:

  • Anionic self-assembled cages are challenging to design due to charge repulsion.
  • Understanding host-guest chemistry in aqueous environments is crucial for applications.

Purpose of the Study:

  • To synthesize water-soluble anionic Fe4L4 cages.
  • To investigate the anion binding properties and selectivity of these cages.
  • To explore the potential of these cages for anion recognition and controlled release.

Main Methods:

  • Multicomponent self-assembly using functionalized trigonal ligands, Fe(II) salts, and sulfonated formylpyridine.
  • Spectroscopic and crystallographic characterization of the cages.
  • Anion binding studies in aqueous solution, including kinetic experiments.

Main Results:

  • Successfully synthesized water-soluble Fe4L4(4-) cages in purely aqueous solution.
  • Demonstrated selective encapsulation of non-coordinating anions (e.g., PF6-, AsF6-) based on size.
  • Observed very slow anion exchange rates due to external negative charge and steric hindrance.

Conclusions:

  • Water-soluble anionic cages can effectively bind specific anions in aqueous media.
  • The slow anion exchange kinetics suggest potential for controlled anion delivery systems.
  • This recognition mechanism could be applied to environmental remediation and anion sequestration.