A Novel Synthesis Strategy for Poly(Arylene‐Vinylene) Derivatives by Elemental Sulfur‐Mediated Polyolefination

Herein, a new synthetic access to poly(arylene-1,2-diarylvinylene) (PAV-DA) derivatives is presented by a novel polyolefination of bifunctional N-tosylhydrazones using base-activated elemental sulfur. PAV-DAs are particularly interesting due to their aggregation-induced emission (AIE) properties, resulting in high solid-state photoluminescence quantum yields. The presented procedure allows the successful synthesis of eight homopolymers and two copolymers with different arylene backbones and aryl side chains from easily accessible monomers, not requiring the use of expensive or highly hazardous materials. The polymers are obtained in good yields and number average molecular weights up to 26.9 kDa. Thermal analysis reveals exceptionally high thermal stability with degradation temperatures as high as 541 °C and glass transition temperatures of up to 263 °C. Furthermore, it is found that the polymer properties are easily adjustable via copolymerization.

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Publication Details

Journal
Macromolecular Rapid Communications
Published
2025-03-26
DOI
https://doi.org/10.1002/marc.202500166
Primary Topic
Luminescence and Fluorescent Materials
Type
article
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article

A Novel Synthesis Strategy for Poly(Arylene‐Vinylene) Derivatives by Elemental Sulfur‐Mediated Polyolefination

Peter Conen, Michaël A. R. Meier, Florian J. O. Niedermaier, Sophia Abou El Mirate
Macromolecular Rapid Communications
Luminescence and Fluorescent Materials
article

A Novel Synthesis Strategy for Poly(Arylene‐Vinylene) Derivatives by Elemental Sulfur‐Mediated Polyolefination

Peter Conen, Michaël A. R. Meier, Florian J. O. Niedermaier, Sophia Abou El Mirate
article en

Abstract

Herein, a new synthetic access to poly(arylene-1,2-diarylvinylene) (PAV-DA) derivatives is presented by a novel polyolefination of bifunctional N-tosylhydrazones using base-activated elemental sulfur. PAV-DAs are particularly interesting due to their aggregation-induced emission (AIE) properties, resulting in high solid-state photoluminescence quantum yields. The presented procedure allows the successful synthesis of eight homopolymers and two copolymers with different arylene backbones and aryl side chains from easily accessible monomers, not requiring the use of expensive or highly hazardous materials. The polymers are obtained in good yields and number average molecular weights up to 26.9 kDa. Thermal analysis reveals exceptionally high thermal stability with degradation temperatures as high as 541 °C and glass transition temperatures of up to 263 °C. Furthermore, it is found that the polymer properties are easily adjustable via copolymerization.

Macromolecular Rapid CommunicationsVol. 46(23)
Karlsruhe Institute of Technology (DE)
Openalex Percentile: Top 96%
Luminescence and Fluorescent Materials
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A Novel Synthesis Strategy for Poly(Arylene‐Vinylene) Derivatives by Elemental Sulfur‐Mediated Polyolefination — Peter Conen, Michaël A. R. Meier, et al. · Macromolecular Rapid Communications (2025) | TGRS Research Map | TGRS