FR3071502B1 - Copolymeres hydrocarbones liquides a deux groupements terminaux ester cyclocarbonate - Google Patents

Copolymeres hydrocarbones liquides a deux groupements terminaux ester cyclocarbonate Download PDF

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Publication number
FR3071502B1
FR3071502B1 FR1759008A FR1759008A FR3071502B1 FR 3071502 B1 FR3071502 B1 FR 3071502B1 FR 1759008 A FR1759008 A FR 1759008A FR 1759008 A FR1759008 A FR 1759008A FR 3071502 B1 FR3071502 B1 FR 3071502B1
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cyclocarbonate
butadiene
poly
terminal groups
ester
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FR3071502A1 (fr
Inventor
Guillaume Michaud
Stephane Fouquay
Frederic Simon
Sophie Guillaume
Jean-Francois Carpentier
Cyril Chauveau
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Centre National de la Recherche Scientifique CNRS
Universite de Rennes 1
Bostik SA
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Centre National de la Recherche Scientifique CNRS
Universite de Rennes 1
Bostik SA
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Priority to FR1759008A priority Critical patent/FR3071502B1/fr
Priority to EP18792974.0A priority patent/EP3688040A1/fr
Priority to PCT/FR2018/052380 priority patent/WO2019063945A1/fr
Priority to US16/651,839 priority patent/US11414516B2/en
Publication of FR3071502A1 publication Critical patent/FR3071502A1/fr
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    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
    • C08G61/025—Polyxylylenes
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    • C08G61/04—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
    • C08G61/06—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds
    • C08G61/08—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
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    • C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
    • C08C19/34—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups
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    • C08C19/34—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups
    • C08C19/40—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups with epoxy radicals
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    • C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
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Abstract

1)Copolymère hydrocarboné comprenant 2 groupements terminaux précédés par une fonction ester et choisis parmi un 2-oxo-1,3-dioxolan-4-yl (ou cyclocarbonate), un dithiocyclocarbonate, un exo-vinylène cyclocarbonate, un 2-oxo-1,3-dioxolen-4-yl, dont la chaîne principale comprend les motifs (I) et (II) où R0 est notamment le radical méthyle ; et dont la masse moléculaire moyenne en nombre Mn est comprise entre 400 et 100 000 g/mol. 2) Procédé de préparation dudit copolymère comprenant : (i) une étape de chauffage d'un bipolymère A statistique choisi parmi un poly(butadiène-isoprène), un poly(butadiène-myrcène) et un poly(butadiène-farnésène ) ; puis (ii) une étape de chauffage du produit formé, en présence d'un agent de transfert de chaîne 3) Utilisation comme adhésif, en mélange avec un composé aminé comprenant au moins deux groupements amines.
FR1759008A 2017-09-28 2017-09-28 Copolymeres hydrocarbones liquides a deux groupements terminaux ester cyclocarbonate Active FR3071502B1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
FR1759008A FR3071502B1 (fr) 2017-09-28 2017-09-28 Copolymeres hydrocarbones liquides a deux groupements terminaux ester cyclocarbonate
EP18792974.0A EP3688040A1 (fr) 2017-09-28 2018-09-27 Copolymeres hydrocarbones liquides a deux groupements terminaux ester cyclocarbonate
PCT/FR2018/052380 WO2019063945A1 (fr) 2017-09-28 2018-09-27 Copolymeres hydrocarbones liquides a deux groupements terminaux ester cyclocarbonate
US16/651,839 US11414516B2 (en) 2017-09-28 2018-09-27 Liquid hydrocarbon-based copolymers bearing two cyclocarbonate ester end groups

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FR1759008 2017-09-28
FR1759008A FR3071502B1 (fr) 2017-09-28 2017-09-28 Copolymeres hydrocarbones liquides a deux groupements terminaux ester cyclocarbonate

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FR3071502B1 true FR3071502B1 (fr) 2020-06-19

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EP (1) EP3688040A1 (fr)
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GB1495555A (en) * 1974-12-03 1977-12-21 Petrov G Method of preparing polyurethanes
JPS5874677A (ja) * 1981-10-30 1983-05-06 Kanebo Ltd 臭素化１，３−ジオキソレン−２−オン類の製造法
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CN102757409B (zh) 2012-07-19 2014-07-16 湖南罗比特化学材料有限公司 一种丙烯酸缩水甘油酯的制备方法
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FR3034770B1 (fr) * 2015-04-10 2017-05-12 Bostik Sa Polymeres hydrocarbones comprenant deux groupements terminaux exo-vinylene cyclocarbonate
JP6748112B2 (ja) 2015-04-23 2020-08-26 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ 環状カーボネート
FR3036399B1 (fr) 2015-05-20 2017-06-16 Bostik Sa Polymeres hydrocarbones comprenant deux groupements terminaux (2-thione-1,3-oxathiolan-4-yl)alkyloxycarbonyle
CA2989696A1 (fr) * 2015-06-18 2016-12-22 Basf Se Copolymeres composes d'exo-vinylene carbonatacrylates cycliques
PL3317324T3 (pl) 2015-06-30 2021-11-02 Evonik Operations Gmbh Wolne od izocyjanianów reaktywne kompozycje poliuretanowe

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FR3071502A1 (fr) 2019-03-29

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