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 Experiment Videos

Tunable clathrates.

M R Caira1, T le Roex, L R Nassimbeni

  • 1Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa.

Chemical Communications (Cambridge, England)
|September 21, 2002
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Crystal form conversion of nevirapine solvates subjected to elevated temperature and humidity: a qualitative study.

Die Pharmazie·2018
Same author

Clathrates of TETROL: selective inclusion of methylcyclohexanones in their energetically unfavorable axial methyl conformations.

Chemical communications (Cambridge, England)·2014
Same author

Ethyl-paraben and nicotinamide mixtures: apparent solubility, thermal behavior and X-ray structure of the 1:1 co-crystal.

Journal of pharmaceutical sciences·2008
Same author

1,3-Dipolar cycloaddition reactions of 1-(4-phenylphenacyl)-1,10-phenanthrolinium N-ylide with activated alkynes and alkenes.

Molecules (Basel, Switzerland)·2007
Same author

Polymorphism of NCX4016, an NO-releasing derivative of acetylsalicylic acid.

Journal of pharmaceutical sciences·2004
Same author

Inclusion compounds of binaphthol with picolines: structures, selectivity and kinetics of desolvation.

Acta crystallographica. Section B, Structural science·2001
Same journal

An intrinsically stretchable nanowire-based sensing patch for wearable analysis of sweat chloride ion composition.

Chemical communications (Cambridge, England)·2026
Same journal

A sterically rigid-flexible balanced NHC-Pd precatalyst for room-temperature solvent-free C-N coupling of benzocyclic amines.

Chemical communications (Cambridge, England)·2026
Same journal

Portable fluorescent conjugated microporous polymer sensor coupled with a smartphone for on-site Fe<sup>3+</sup> detection in water.

Chemical communications (Cambridge, England)·2026
Same journal

Accelerated discovery of NO<sub>3</sub>RR single-atom catalysts <i>via</i> high-throughput DFT and machine learning.

Chemical communications (Cambridge, England)·2026
Same journal

Wafer-scale robust graphene electronics under industrial processing conditions.

Chemical communications (Cambridge, England)·2026
Same journal

Subnanoscale IrW oxide anodes: breaking immiscibility for high activity and durability in water electrolysis.

Chemical communications (Cambridge, England)·2026
See all related articles

A diol organic host selectively forms five inclusion compounds with dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) mixtures. Compound stoichiometry changes with guest mixture composition, and their structures are detailed.

Area of Science:

  • Supramolecular Chemistry
  • Crystal Engineering
  • Host-Guest Chemistry

Background:

  • Organic hosts are crucial for selective guest molecule recognition and encapsulation.
  • Understanding host-guest interactions in liquid mixtures is vital for separation and storage applications.
  • Diol-based organic hosts offer unique binding capabilities due to hydrogen bonding.

Purpose of the Study:

  • To investigate the selectivity of a specific diol organic host for dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) mixtures.
  • To characterize the inclusion compounds formed between the diol host and the liquid guest mixture.
  • To elucidate the relationship between guest mixture composition and the stoichiometry of the resulting inclusion compounds.

Main Methods:

  • Synthesis and characterization of inclusion compounds using techniques such as X-ray crystallography.

Related Experiment Videos

  • Analysis of guest mixture composition and its correlation with host-guest stoichiometry.
  • Structural determination of the five distinct inclusion compounds formed.
  • Main Results:

    • The diol organic host demonstrated selective complexation with mixtures of DMF and DMSO.
    • Five distinct inclusion compounds were successfully isolated and characterized.
    • The stoichiometry of these compounds varied in discrete steps, directly correlating with the composition of the liquid guest mixture.

    Conclusions:

    • The diol organic host exhibits tunable selectivity for DMF/DMSO mixtures, forming discrete stoichiometric compounds.
    • The study provides detailed structural insights into these supramolecular assemblies.
    • Findings contribute to the design of selective host materials for liquid mixtures.