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

You might also read

Related Articles

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

Sort by
Same author

An electronic equilibrium strategy to drive the design of reversible fluorescent probes for sulfur dioxide and formaldehyde.

Chemical science·2026
Same author

Enzyme-Activatable Fluorogenic Probes: Design Strategies, Biomedical Applications, and Future Perspectives.

Journal of the American Chemical Society·2026
Same author

Photocaged Fluorogenic Glycoprobes for Light-Activatable Sensing and Imaging of Galactosidase Activities in Live Cells.

ACS sensors·2026
Same author

Synthesis of divalent galactosyl and fucosyl spiropyran derivatives for the targeted inhibition of bacterial biofilms.

Chemical communications (Cambridge, England)·2026
Same author

A novel water-soluble near-infrared fluorescent probe for monitoring viscosity fluctuations in plants and zebrafish under abiotic stresses.

Smart molecules : open access·2026
Same author

Spatiotemporal analysis of reactive oxygen species using specific activity-based sensing fluorescent imaging probes.

Nature reviews. Chemistry·2026

Related Experiment Video

Updated: Jun 6, 2026

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores
09:46

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores

Published on: August 19, 2013

Boronic acid building blocks: tools for sensing and separation.

Ryuhei Nishiyabu1, Yuji Kubo, Tony D James

  • 1Department of Applied Chemistry, Graduate School of Urban Environmental Sciences, Tokyo Metropolitan University, 1-1, Minami-ohsawa, Hachioji, Tokyo 192-0397, Japan.

Chemical Communications (Cambridge, England)
|December 1, 2010
PubMed
Summary

Boronic acids are versatile tools for detecting and separating analytes like saccharides and anions. Their reversible interactions enable applications in molecular sensing and boron affinity chromatography.

More Related Videos

A Polyaniline-based Sensor of Nucleic Acids
07:58

A Polyaniline-based Sensor of Nucleic Acids

Published on: November 1, 2016

Microfluidic On-chip Capture-cycloaddition Reaction to Reversibly Immobilize Small Molecules or Multi-component Structures for Biosensor Applications
14:43

Microfluidic On-chip Capture-cycloaddition Reaction to Reversibly Immobilize Small Molecules or Multi-component Structures for Biosensor Applications

Published on: September 23, 2013

Related Experiment Videos

Last Updated: Jun 6, 2026

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores
09:46

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores

Published on: August 19, 2013

A Polyaniline-based Sensor of Nucleic Acids
07:58

A Polyaniline-based Sensor of Nucleic Acids

Published on: November 1, 2016

Microfluidic On-chip Capture-cycloaddition Reaction to Reversibly Immobilize Small Molecules or Multi-component Structures for Biosensor Applications
14:43

Microfluidic On-chip Capture-cycloaddition Reaction to Reversibly Immobilize Small Molecules or Multi-component Structures for Biosensor Applications

Published on: September 23, 2013

Area of Science:

  • Analytical Chemistry
  • Materials Science

Background:

  • Boronic acids are key reagents for recognizing diol motifs via boronic ester formation and interacting with anions to form boronates.
  • These interactions are foundational for developing molecular sensors and separation techniques for various analytes.

Purpose of the Study:

  • To review the applications of boronic acids in monitoring, identifying, and isolating analytes.
  • To survey the use of boronic acid-diol and anion interactions in sensing and separation protocols.

Main Methods:

  • Exploitation of boronic acid-diol interactions for boronic ester formation.
  • Utilization of boronic acid-anion interactions for the generation of boronates.
  • Application of these interactions in sensing and separation protocols, including boron affinity chromatography.

Main Results:

  • Boronic acids have demonstrated success in monitoring diverse analytes.
  • Reversible boronic acid-diol interactions have enabled new separation domains through boron affinity chromatography.
  • The development of robust molecular sensors for selective analyte detection is highlighted.

Conclusions:

  • Boronic acids offer a versatile platform for analyte sensing and separation across physiological, environmental, and industrial settings.
  • The unique binding properties of boronic acids facilitate the development of advanced analytical tools.
  • Continued research into boronic acid chemistry promises further innovation in molecular recognition and purification.