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

Solvents01:12

Solvents

70.0K
A solvent is a substance, most often a liquid, that can dissolve other substances. Here, the substance being dissolved is called a solute. When a solvent and a solute combine, they form a solution - a homogenous mixture of both the solvent and the solute. Water is a universal biological solvent. Its polar structure allows it to dissolve many other polar compounds. The ability of water to dissolve is governed by a balance between water molecules binding to each other and binding to the solute.
A...
70.0K
Rotary Evaporation to Remove Solvent06:43

Rotary Evaporation to Remove Solvent

217.7K
Source: Dr. Melanie Pribisko Yen and Grace Tang — California Institute of Technology
Rotary evaporation is a technique most commonly used in organic chemistry to remove a solvent from a higher-boiling point compound of interest. The rotary evaporator, or "rotovap", was invented in 1950 by the chemist Lyman C. Craig. The primary use of a rotovap is to dry and purify samples for downstream applications. Its speed and ability to handle large volumes of solvent make rotary...
217.7K
Self-Assembly of Gamma-Modified Peptide Nucleic Acids into Complex Nanostructures in Organic Solvent Mixtures08:15

Self-Assembly of Gamma-Modified Peptide Nucleic Acids into Complex Nanostructures in Organic Solvent Mixtures

4.6K
This article provides protocols for the design and self-assembly of nanostructures from gamma-modified peptide nucleic acid oligomers in organic solvent...
4.6K
Titration in Nonaqueous Solvents01:16

Titration in Nonaqueous Solvents

1.3K
Most acid-base titrations are performed in an aqueous medium. In aqueous titrations, water competes with weaker acids or bases for proton donation or acceptance, leading to ambiguous endpoints in the titration curve. Water also affects the partial ionization of weak acids or bases. For example, water accepts a proton from acetic acid to form hydronium and acetate ions. The hydronium ion formed is a stronger acid than acetic acid, and the acetate ion is a stronger base than water. As a result,...
1.3K
Schlenk Lines Transfer of Solvents09:41

Schlenk Lines Transfer of Solvents

43.6K
Source: Hsin-Chun Chiu and Tyler J. Morin, laboratory of Dr. Ian Tonks—University of Minnesota Twin Cities
Schlenk lines and high vacuum lines are both used to exclude moisture and oxygen from reactions by running reactions under a slight overpressure of inert gas (usually N2 or Ar) or under vacuum. Vacuum transfer has been developed as a method separate solvents (other volatile reagents) from drying agents (or other nonvolatile agents) and dispense them to reaction or storage vessels...
43.6K
Preparation of Biopolymer Aerogels Using Green Solvents08:13

Preparation of Biopolymer Aerogels Using Green Solvents

18.3K
A new way for the production of biopolymer-based aerogels by carbon dioxide (CO2) induced gelation is shown. The technique utilizes pressurized carbon dioxide (5 MPa) for the production of biopolymer hydrogels and supercritical CO2 (12 MPa) to convert gels into aerogels. The only solvents needed besides CO2 are water and...
18.3K

You might also read

Related Articles

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

Sort by
Same author

Synthesis, crystal structure and Hirshfeld surface analysis of 2-(2,5-dioxo-4,4-di-phenyl-imidazolidin-1-yl)-<i>N</i>-(4-fluoro-phen-yl)acetamide (phenytoin analog).

Acta crystallographica. Section E, Crystallographic communications·2026
Same author

Automated serial electron diffraction: implementation in <i>LibraEDT</i> and its applications.

Journal of applied crystallography·2026
Same author

Through-space donor-acceptor homoconjugation strategies for emissive radical species.

Chemical science·2026
Same author

1-Ethenyl-2-(methyl-sulfan-yl)-4,4-diphenyl-4,5-di-hydro-1<i>H</i>-imidazol-5-one (Thio-phenytoin analogue): synthesis, structure and Hirshfeld surface analysis.

Acta crystallographica. Section E, Crystallographic communications·2026
Same author

Ultrasensitive Hydrogen Detection via Layered n-Type Polymer Chemiresistors.

Nano letters·2026
Same author

Photoactive PFA Coating through Fluorophilic Interactions for Continuous Flow Photochemistry.

JACS Au·2025
Same journal

Non-radical peroxymonosulfate activation by Co-doped InBO<sub>3</sub>: a green route for selective benzyl alcohol oxidation.

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

Interfacial engineering of ultrahigh-performance sandwich-structured composites for multifunctional electromagnetic shielding, infrared stealth, and self-cleaning.

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

Photoinduced CO and NO release of cyclopentadienyl ruthenium(II) complexes bearing <i>N</i>,<i>N</i>-chelate ligands.

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

Hydrothermal synthesis of well-known iridium complexes with ammonia ligands.

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

Decoupling oxygen sensitivity and aggregation effects in a dual-emissive platinum(II) chlorin lifetime probe.

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

Exploration of the role of carboxylate bridges on the magnetisation dynamics of {LnIII2} (Ln = Tb, Dy, Ho, and Er) paddle-wheel single-molecule magnets: structure-property correlations.

Dalton transactions (Cambridge, England : 2003)·2026
See all related articles

Related Experiment Video

Updated: Jan 20, 2026

Self-Assembly of Gamma-Modified Peptide Nucleic Acids into Complex Nanostructures in Organic Solvent Mixtures
08:15

Self-Assembly of Gamma-Modified Peptide Nucleic Acids into Complex Nanostructures in Organic Solvent Mixtures

Published on: June 26, 2020

4.6K

Solvent-responsive cavitand lanthanum complex.

Francesca Guagnini1, Alessandro Pedrini, Timothy M Swager

  • 1Dipartimento di Scienze Chimiche, della Vita e della SostenibilitĂ  Ambientale and INSTM UdR Parma, UniversitĂ  di Parma, Parco Area delle Scienze 17/A, 43123 Parma (PR), Italy.

Dalton Transactions (Cambridge, England : 2003)
|August 31, 2019
PubMed
Summary
This summary is machine-generated.

Researchers created a novel solvent-responsive complex using a cavitand-lanthanum coordination. This supramolecular assembly changes structure in different solvents like acetonitrile and acetone, demonstrating dynamic molecular architecture control.

More Related Videos

Rotary Evaporation to Remove Solvent
06:43

Rotary Evaporation to Remove Solvent

Published on: April 30, 2023

217.7K
Solvents and Sphere of Hydration
01:12

Solvents and Sphere of Hydration

70.0K

Related Experiment Videos

Last Updated: Jan 20, 2026

Self-Assembly of Gamma-Modified Peptide Nucleic Acids into Complex Nanostructures in Organic Solvent Mixtures
08:15

Self-Assembly of Gamma-Modified Peptide Nucleic Acids into Complex Nanostructures in Organic Solvent Mixtures

Published on: June 26, 2020

4.6K
Rotary Evaporation to Remove Solvent
06:43

Rotary Evaporation to Remove Solvent

Published on: April 30, 2023

217.7K
Solvents and Sphere of Hydration
01:12

Solvents and Sphere of Hydration

70.0K

Area of Science:

  • Supramolecular Chemistry
  • Coordination Chemistry
  • Materials Science

Background:

  • Stimuli-responsive supramolecular assemblies are key for dynamic systems.
  • Metal coordination is a reliable method for creating responsive architectures.
  • Cavitands offer unique structural frameworks for molecular recognition.

Purpose of the Study:

  • To prepare and characterize a novel solvent-responsive cavitand-lanthanum coordination complex.
  • To investigate the influence of different solvents on the complex's architecture.
  • To demonstrate the dynamic switching capabilities of the supramolecular assembly.

Main Methods:

  • Synthesis of a tetra-phosphonate cavitand functionalized with hydroxyl groups.
  • Coordination of the functionalized cavitand with lanthanum salts.
  • Characterization using NMR spectroscopy, Isothermal Titration Calorimetry (ITC), and single-crystal X-ray diffraction.
  • Analysis of solvent-induced structural changes using DOSY-NMR spectroscopy.

Main Results:

  • A pre-organized octadentate ligand was formed from the functionalized cavitand.
  • Two distinct complex architectures were observed in acetonitrile and acetone.
  • The single crystal structure of the acetonitrile derivative was determined.
  • Small amounts of acetone in acetonitrile induced assembly interconversion, confirmed by DOSY-NMR.

Conclusions:

  • A novel solvent-responsive cavitand-lanthanum complex was successfully prepared.
  • The complex exhibits distinct architectures in different organic solvents.
  • The system demonstrates tunable supramolecular assembly through solvent-induced switching.