Bio-based aliphatic primary amines from alcohols through the ‘Nitrile route’ towards non-isocyanate polyurethanes

Abstract : Bio-based primary amines obtained from the corresponding alcohols via nitrile intermediates and their subsequent polymerizations with cyclic carbonates are described. Nitrile compounds were synthesized under mild aerobic oxidation of primary aliphatic alcohols. CuI, bipyridine and TEMPO were used as a catalytic system, in the presence of aqueous ammonia and O2. A series of bio-sourced alcohols were successfully oxidized into nitriles using this catalytic system. The so-formed bio-based dinitriles were subsequently reduced into primary diamines under H2 in the presence of Ni Raney. The latter were polymerized with fatty acid-based bis-cyclic carbonates for the design of fully bio-based poly(hydroxyurethane)s.
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https://hal.archives-ouvertes.fr/hal-01373151
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Submitted on : Wednesday, September 28, 2016 - 11:18:24 AM
Last modification on : Thursday, January 11, 2018 - 6:28:10 AM

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Geoffrey Hibert, Oceane Lamarzelle, Lise Maisonneuve, Etienne Grau, Henri Cramail. Bio-based aliphatic primary amines from alcohols through the ‘Nitrile route’ towards non-isocyanate polyurethanes. European Polymer Journal, Elsevier, 2016, 82, pp.114-121. ⟨10.1016/j.eurpolymj.2016.07.007⟩. ⟨hal-01373151⟩

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