PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
February 5, 2026Angewandte Chemie0 citations

Living Polymerization Strategy for Conjugated Multiblock Copolymers: A Systematic Study of Structure–Property Relationships in Stretchability and Charge Transport

View Full Paper
HYHee‐Seong YangHYHyeonjin YooYKYejin Kim

Key Points

  • The aim is to systematically investigate how structural parameters affect the performance of stretchable conjugated polymers.
  • Constructed a library of poly(3-hexylthiophene) precursors with varied molecular weight and dispersity.
  • Incorporated precursors into conjugated multiblock copolymers with flexible polydimethylsiloxane.
  • Varied the composition of the copolymers to analyze different structural parameters.
  • CMPs with well-defined P3HT blocks showed stretchability over 300%.
  • High hole mobility was maintained in well-defined CMPs, unlike those using uncontrolled polymerization.

Abstract

ABSTRACT Achieving high mechanical stretchability while maintaining charge carrier mobility in semiconducting polymers remains a central challenge due to their intrinsic trade‐off. Conjugated multiblock copolymers (CMPs) incorporating semiconducting and elastomeric segments represent a promising design strategy to overcome this limitation, yet a systematic understanding of how structural parameters influence material properties and device performances is still lacking. To address this issue, we chose a model polymer, poly(3‐hexylthiophene) (P3HT), and systematically constructed its library precursors with independently varied molecular weight, dispersity, and end‐group fidelity. Then, these precursors were incorporated into CMPs containing flexible polydimethylsiloxane (PDMS) over a broad composition range (0–75 mol%). As a result, this design enabled deconvolution of the individual effects of each structural parameter on CMP performance. Notably, CMPs incorporating well‐defined P3HT blocks exhibited significantly enhanced stretchability (>300%) while retaining high hole mobility, in contrast to those prepared using P3HT from uncontrolled polymerization. These results underscore the advantage of living polymerization in precisely tailoring conjugated polymer architectures and optimizing the mechanical and electronic properties of stretchable semiconducting materials, while also offering a platform that may be extended to other conjugated polymers.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Yang et al. (2026) studied this question.

synapsesocial.com/papers/69843451f1d9ada3c1fb25b2https://doi.org/10.1002/ange.202523558
Ask AI
Helpful
Bookmark
Share
View Full Paper