Diarylbiindolinones as Substituent-Tunable Mechanochromophores and Their Application in Mechanochromic Polymers.

Clicks: 246
ID: 71668
2019
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #35 of 79 articles by views in Macromolecular rapid communications

Most read Least read

Bar heights use a square-root scale.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Sign in to mint
Abstract
The synthesis and characterization of a series of diarylbiindolinone derivatives as substituent-tunable mechanochromophores that generate pink carbon-centered radicals in response to mechanical stimuli are reported. The changes in mechano-responsiveness, which result from the introduction of various substituents on the diarylbiindolinone skeleton, are systematically studied and mechanochromic polymers that contain such diarylbiindolinone units are developed.
Reference Key
kawasaki2019diarylbiindolinonesmacromolecular Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Kawasaki, Kazuma;Aoki, Daisuke;Otsuka, Hideyuki;
Journal Macromolecular rapid communications
Year 2019
DOI
10.1002/marc.201900460
URL
Keywords
mechanochemistry radicals diarylbiindolinone mechanochromic polymers mechanophores

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

Comments

No comments yet. Be the first to comment on this article.