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

Reactive block copolymer scaffolds.

Ronald C Li1, Jungyeon Hwang, Heather D Maynard

  • 1Department of Chemistry and Biochemistry & California Nanosystems Institute, University of California, Los Angeles, CA 90095-1569, USA.

Chemical Communications (Cambridge, England)
|August 31, 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

Traceless linkers used for reversible protein-polymer conjugations.

Chemical science·2026
Same author

An Orally Administered Misuse Deterrent Opioid Prodrug for Treatment of Acute Pain.

JACS Au·2025
Same author

Important design rules discovered for supramolecular multivalent ligands interacting with dynamic receptors.

Proceedings of the National Academy of Sciences of the United States of America·2025
Same author

Biosourced Functional Hydroxybenzoate-<i>co</i>-Lactide Polymers with Antimicrobial Activity.

Journal of the American Chemical Society·2025
Same author

<i>In silico</i> screening of <i>P</i>,<i>N</i>-ligands facilitates optimization of Au(iii)-mediated <i>S</i>-arylation.

Chemical science·2025
Same author

Electronic Effects of Bidentate <i>P</i>,<i>N</i>-Ligands on the Elementary Steps of Au(I)/Au(III) Reactions Relevant to Cross-Coupling Chemistry.

Organic letters·2024
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

Researchers synthesized block copolymers with varying reactivity sequences. They demonstrated step-wise, selective modification to create new block copolymer materials.

Area of Science:

  • Polymer Chemistry
  • Materials Science

Background:

  • Block copolymers are versatile macromolecules with unique properties arising from their distinct polymer segments.
  • Precise control over block copolymer architecture is crucial for tailoring material properties.

Purpose of the Study:

  • To synthesize novel block copolymers with sequences exhibiting differential reactivity.
  • To demonstrate the capability of selective, step-wise derivatization for creating new block copolymer structures.

Main Methods:

  • Synthesis of block copolymers featuring segments with distinct chemical reactivities.
  • Utilizing controlled chemical reactions to selectively modify one block over another.

Main Results:

  • Successful synthesis of block copolymers with designed differential reactivity.

Related Experiment Videos

  • Demonstration of step-wise derivatization, enabling the formation of new, precisely defined block copolymers.
  • Conclusions:

    • The developed synthetic strategy allows for controlled, sequential modification of block copolymers.
    • This approach offers a pathway to novel block copolymer architectures with tailored functionalities.