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

Noncovalent Synthesis Using Hydrogen Bonding.

Leonard J. Prins1, David N. Reinhoudt, Peter Timmerman

  • 1Laboratory of Supramolecular Chemistry and Technology MESA(+) Research Institute University of Twente P.O. Box 217, 7500 AE Enschede (The Netherlands).

Angewandte Chemie (International Ed. in English)
|July 10, 2001
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

Controlling Tricyclic Peptide Architecture in mRNA Display through Orthogonal Reactivity on Rotationally Flexible Scaffolds.

ACS chemical biology·2026
Same author

Chemokine-Binding All-D-CLIPS Peptides Identified Using Mirror-Image Phage Display.

ACS chemical biology·2025
Same author

Molecular Detection of Venous Thrombosis in Mouse Models Using SPECT/CT.

Biomolecules·2022
Same author

Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels.

Biomaterials science·2021
Same author

A Phase I Open-Label Clinical Trial Evaluating the Therapeutic Vaccine hVEGF26-104/RFASE in Patients with Advanced Solid Malignancies.

The oncologist·2020
Same author

High-Affinity α<sub>5</sub>β<sub>1</sub>-Integrin-Selective Bicyclic RGD Peptides Identified via Screening of Designed Random Libraries.

ACS combinatorial science·2019

Hydrogen bonds, though individually weak, exhibit cooperativity for enhanced strength. This principle underpins noncovalent synthesis, enabling the creation of stable chemical structures and novel materials.

Area of Science:

  • Organic Chemistry
  • Supramolecular Chemistry
  • Materials Science

Background:

  • Hydrogen bonds are weak individually but display cooperativity, a phenomenon where combined strength exceeds the sum of individual interactions.
  • This '1+1 > 2' principle is fundamental to understanding the stability of molecular assemblies.
  • Over two decades of research have established noncovalent synthesis as a distinct field in organic chemistry.

Purpose of the Study:

  • To review noncovalent synthesis strategies relying on the reversible formation of multiple hydrogen bonds.
  • To elucidate the fundamental principles governing the stability of hydrogen-bond-mediated assemblies.
  • To highlight applications in areas such as encapsulation, self-replication, and novel materials development.

Main Methods:

Related Experiment Videos

  • Detailed description of hydrogen bond characteristics and their cooperative behavior.
  • Analysis of bimolecular and higher-order assemblies formed through hydrogen bonding.
  • Exploration of principles governing the stability and function of these assemblies.
  • Main Results:

    • Demonstration of how cooperativity enhances the stability of hydrogen-bonded structures.
    • Examples of reversible capsules exhibiting encapsulation phenomena.
    • Discussion of hydrogen bonding's role in self-replication and the formation of dynamic libraries.

    Conclusions:

    • Noncovalent synthesis utilizing hydrogen bonds offers a powerful approach for designing stable and functional molecular systems.
    • This field has led to the development of advanced materials like nanotubes, liquid crystals, and polymers.
    • The principles of hydrogen bonding continue to drive innovation in supramolecular chemistry and materials science.