4.7 Article

Room-temperature Barbier single-atom polymerization induced emission as a versatile approach for the utilization of monofunctional carboxylic acid resources

Journal

POLYMER CHEMISTRY
Volume 13, Issue 5, Pages 592-599

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1py01493e

Keywords

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Funding

  1. NSFC [21971236, 21922112, 21672213, 21871258]
  2. State Key Laboratory of Molecular Engineering of Polymers (Fudan University) [K2020-27]
  3. National Key R&D Program of China [2017YFA0700103]
  4. Haixi Institute of CAS [CXZX-2017-P01]

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This study demonstrates a versatile approach, called Barbier single-atom polymerization, for the utilization of monofunctional carboxylic acid resources to prepare polymers with specific luminescent properties. The synthesized polymers have potential applications in material science, artificial light-harvesting systems, and explosive detection.
Carboxylic acids are widely available from both biomass and fossil sources on the Earth. In comparison with multifunctional carboxylic acid containing chemicals that have been comprehensively used as building blocks of polymer materials, monofunctional carboxylic acid resources exhibit broader availability but are rarely utilized as monomers for polymerization, attributed to their monofunctionality. Here, we demonstrate a Barbier single-atom polymerization (SAP) as a versatile approach for the utilization of monofunctional carboxylic acid resources, where they act as a carbon source to contribute only one carbon atom for the construction of the polymer main chain. The key point for the polymerization of the monofunctional carboxylic acid resource is to difunctionalize it, which is realized through two Barbier additions between bifunctional aromatic halides and monofunctional peroxyester in the presence of Mg. Prior to the Barbier SAP, monofunctional phenylcarboxylic acid is converted into dibenzoyl peroxide (BPO) with higher reactivity. Through the Barbier SAP of BPO at room temperature, a series of nonconjugated polytriphenylmethanols (PTPMs) were prepared as polymerization-induced emission luminogens (PIEgens) with structure-specific nonconjugated luminescence including aggregation-caused quenching (ACQ) and aggregation induced emission (AIE) characteristics, where starting monomers and repeating units are nonemissive. Further applications of PIEgens were carried out for an artificial light-harvesting system with an antenna effect of over 18.5 and explosive detection at the ppm level in solution and ng level on test paper. This work therefore opens a new avenue for the design of nonconjugated luminescence by utilizing Earth's monofunctional carboxylic acid resources sufficiently.

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