The application of the Diels-Alder reaction to polymers bearing furan moieties .1. Reactions with maleimides
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Laita, H
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INST NATL POLYTECH GRENOBLE,ECOLE FRANCAISE PAPETERIE & IND GRAPH,F-38402 ST MARTIN DHER,FRANCEINST NATL POLYTECH GRENOBLE,ECOLE FRANCAISE PAPETERIE & IND GRAPH,F-38402 ST MARTIN DHER,FRANCE
Laita, H
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Boufi, S
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INST NATL POLYTECH GRENOBLE,ECOLE FRANCAISE PAPETERIE & IND GRAPH,F-38402 ST MARTIN DHER,FRANCEINST NATL POLYTECH GRENOBLE,ECOLE FRANCAISE PAPETERIE & IND GRAPH,F-38402 ST MARTIN DHER,FRANCE
Boufi, S
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Gandini, A
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INST NATL POLYTECH GRENOBLE,ECOLE FRANCAISE PAPETERIE & IND GRAPH,F-38402 ST MARTIN DHER,FRANCEINST NATL POLYTECH GRENOBLE,ECOLE FRANCAISE PAPETERIE & IND GRAPH,F-38402 ST MARTIN DHER,FRANCE
Gandini, A
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[1] INST NATL POLYTECH GRENOBLE,ECOLE FRANCAISE PAPETERIE & IND GRAPH,F-38402 ST MARTIN DHER,FRANCE
Two types of furan-containing polymers, namely polyurethanes and acrylic copolymers, were used as reactive substrates for Diels-Alder cycloadditions with mono- and bis-maleimides. The role of the specific position of the heterocycle in the macromolecular chains, as well as its frequency along them, was studied in order to assess the ease with which the coupling occurred. Both the simple adducts derived from the monofunctional dienophiles and the crosslinked products arising from the coupling of the furanic polymers with the bisdienophiles were fully characterized. Attempts to return to linear structures by heating the latter materials, cia the retro Diels-Alder reaction, were not successful. (C) 1997 Elsevier Science Ltd.
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Tokyo Denki Univ, Dept Mat & Life Sci, Grad Sch Adv Sci & Technol, Chiyoda Ku, Tokyo 1018457, JapanTokyo Denki Univ, Dept Mat & Life Sci, Grad Sch Adv Sci & Technol, Chiyoda Ku, Tokyo 1018457, Japan
Xawkat, Ahmat
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Ablajan, Keyume
Hiraku, Shinozaki
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Tokyo Denki Univ, Dept Mat & Life Sci, Grad Sch Adv Sci & Technol, Chiyoda Ku, Tokyo 1018457, JapanTokyo Denki Univ, Dept Mat & Life Sci, Grad Sch Adv Sci & Technol, Chiyoda Ku, Tokyo 1018457, Japan