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April 27, 2026Macromolecules0 citations

Multifunctional Solid-State Emissive 1D Conjugated Polymer with On-Demand Electrochemical or Chemical Reactivity for 3D Polymerization

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SSSanjib SarmahInstitute of Molecular Functional MaterialsMBMridusmita BuragohainUniversity of HyderabadMBManas Kumar BeraInstitute of Molecular Functional Materials

Key Points

  • The aim is to develop a multifunctional 1D conjugated polymer with solid-state emission and chemical reactivity.
  • Developed 1D conjugated polymer PFtBTPA through rational molecular design.
  • Achieved reversible redox activity and near-infrared electrochromism at low potential (<0.7 V).
  • Enabled electrochemical or chemical 3D polymerization via functional side groups.
  • 1D PFtBTPA shows solid-state emission with enhanced multifunctionality.
  • Demonstrates reversible redox activity and electrochromism, suggesting versatility in applications.
  • Facilitated on-demand 3D polymerization, expanding the functional polymer platform.

Abstract

Deriving multifunctionality in solid-state emissive conjugated polymers (CPs) remains of great interest for further advancement in the synthesis of new functional polymers and to expand their scope of applications. Here, we demonstrate a rational molecular structural design and synthesis of a 1D conjugated polymer (PFtBTPA) to achieve not only solid-state emission but also multifunctional behavior. Introducing a partially twisted structure within PFtBTPA gives rise to emission in the solid state, and the functional side groups attached to the polymer chain empower reversible redox activity and near-infrared (NIR) electrochromism as well as electrofluorochromism at low potential (<0.7 V). The 1D PFtBTPA further undergoes on-demand electrochemical or chemical 3D polymerization via coupling of functional side groups, which again opens a platform to create functional 3D polymers. This development may provide a new impetus for polymer chemistry and materials science research.

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Cite This Study

Sarmah et al. (2026) studied this question.

synapsesocial.com/papers/69eefd9bfede9185760d44cdhttps://doi.org/10.1021/acs.macromol.5c02591
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