Thermal Behavior of New Polymaleamides

Găină, Constantin; Ursache, Oana; Gaina, Viorica

doi:10.1080/03602559.2013.844248

Cited by 2 publications

(1 citation statement)

References 31 publications

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“…Polycondensation by fmDA reaction using bifunctional linear monomers (bis-furans and bis-maleimides) or polymerization of maleimide-substituted furans was applied in the development of various linear dynamers [85][86][87][88], including polymers with switchable optical properties [89,90] or magnetically active conjugates [91]. A significant limitation of this approach is the low degrees of polymerization by fmDA reaction (Table 4).…”

Section: Synthesis Of Dynamic Linear Polymers Using the Fmda "Click" Reactionmentioning

confidence: 99%

Diels–Alder Cycloadditions of Bio-Derived Furans with Maleimides as a Sustainable «Click» Approach towards Molecular, Macromolecular and Hybrid Systems

2021

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This mini-review highlights the recent research trends in designing organic or organic-inorganic hybrid molecular, biomolecular and macromolecular systems employing intermolecular Diels–Alder cycloadditions of biobased, furan-containing substrates and maleimide dienophiles. The furan/maleimide Diels–Alder reaction is a well-known process that may proceed with high efficiency under non-catalytic and solvent-free conditions. Due to the simplicity, 100% atom economy and biobased nature of many furanic substrates, this type of [4+2]-cycloaddition may be recognized as a sustainable “click” approach with high potential for application in many fields, such as fine organic synthesis, bioorganic chemistry, material sciences and smart polymers development.

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