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

Hydroxy-cruciforms.

Psaras L McGrier1, Kyril M Solntsev, Jan Schönhaber

  • 1School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332, USA.

Chemical Communications (Cambridge, England)
|May 24, 2007
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

Olefin-Linked Cationic Covalent Organic Frameworks as Host Materials for Lithium-Sulfur Batteries.

ACS applied materials & interfaces·2025
Same author

Ring Contraction of Cyclooctatetraenes toward Non-Benzenoid Polycyclic Aromatic Hydrocarbons by Au(111)-Catalysis and Bulk Pyrolysis.

Chemistry (Weinheim an der Bergstrasse, Germany)·2025
Same author

Steering Magnetic Coupling in Diradical Nonbenzenoid Nanographenes.

Journal of the American Chemical Society·2025
Same author

Exceptionally High Two-Photon Absorption Cross Sections in Quinoidal Diazaacene-Bithiophene Derivatives.

Angewandte Chemie (International ed. in English)·2025
Same author

A Thienothiophene-Based Olefin-Linked Covalent Organic Framework for the Metal-Free Photocatalytic Oxidative Coupling of Amines.

ACS macro letters·2025
Same author

Photocatalytic applications of covalent organic frameworks: synthesis, characterization, and utility.

Nanoscale·2024

Hydroxy-cruciforms 7 and 8 were synthesized and demonstrated significant changes in their photophysical properties when exposed to amines. This highlights their potential for amine sensing applications.

Area of Science:

  • Organic Chemistry
  • Photophysics
  • Materials Science

Background:

  • Cruciform molecules are a class of compounds with unique structural and electronic properties.
  • Photophysical properties of organic molecules are crucial for applications in sensing and imaging.
  • Amine detection remains an important challenge in various scientific fields.

Purpose of the Study:

  • To report the synthesis of novel hydroxy-cruciforms 7 and 8.
  • To investigate the photophysical properties of these hydroxy-cruciforms.
  • To explore their response to amine exposure for potential sensing applications.

Main Methods:

  • Synthesis of hydroxy-cruciforms 7 and 8 using established organic chemistry techniques.
  • Characterization of the synthesized compounds using spectroscopic methods (e.g., NMR, Mass Spectrometry).

Related Experiment Videos

  • Evaluation of photophysical properties including absorption, emission, and quantum yield, and their changes upon addition of various amines.
  • Main Results:

    • Successful synthesis and characterization of hydroxy-cruciforms 7 and 8.
    • Demonstrated dramatic and varying changes in photophysical properties (e.g., fluorescence intensity, emission wavelength) of compounds 7 and 8 upon exposure to different amines.
    • The observed photophysical changes are dependent on the type and concentration of the amine.

    Conclusions:

    • Hydroxy-cruciforms 7 and 8 exhibit significant and tunable responses to amines.
    • These findings suggest that hydroxy-cruciforms are promising candidates for the development of novel amine sensors.
    • Further studies can explore the mechanism of interaction and optimize the sensor performance.