Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
  • C08F214/18—Monomers containing fluorine
  • C08F214/22—Vinylidene fluoride
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2/00—Processes of polymerisation
  • C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
  • C08F214/18—Monomers containing fluorine
  • C08F214/28—Hexyfluoropropene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F4/00—Polymerisation catalysts
  • C08F4/28—Oxygen or compounds releasing free oxygen
  • C08F4/30—Inorganic compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/04—Reduction, e.g. hydrogenation
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/12—Hydrolysis
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/02—Halogenated hydrocarbons
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/13—Phenols; Phenolates
  • C08K5/136—Phenols containing halogens
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/16—Nitrogen-containing compounds
  • C08K5/34—Heterocyclic compounds having nitrogen in the ring
  • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
  • C08K5/3477—Six-membered rings
  • C08K5/3492—Triazines
  • C08K5/34922—Melamine; Derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
  • C08K5/37—Thiols
  • C08K5/372—Sulfides, e.g. R-(S)x-R'
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/54—Silicon-containing compounds
  • C08K5/541—Silicon-containing compounds containing oxygen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
  • C08L27/22—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers modified by chemical after-treatment
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
  • C08F2800/10—Copolymer characterised by the proportions of the comonomers expressed as molar percentages
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2810/00—Chemical modification of a polymer
  • C08F2810/40—Chemical modification of a polymer taking place solely at one end or both ends of the polymer backbone, i.e. not in the side or lateral chains

Definitions

• the present invention relates to functional fluorinated copolymers obtained from vinylidene fluoride (VDF) monomers and tetrafluoropropene, as well as processes for the preparation of these polymers.
• VDF vinylidene fluoride
• Fluoropolymers are a class of compounds with outstanding properties for a wide range of applications, from paint and specialty coatings to seals, optics, microelectronics, separators, bonding agents, and more. electrodes and electrolytes for lithium ion batteries, and membrane technology.
• the vinylidene fluoride-based copolymers are particularly interesting because of their diversity, their morphology, their exceptional properties and their versatility.
• US 3,085,996 discloses the preparation of copolymers based on 2,3,3,3-tetrafluoropropene (1234yf) and VDF or various other fluorinated monomers, according to an aqueous emulsion polymerization process.
• the document WO 2013/160621 describes the manufacture of copolymers by controlled radical copolymerization based on trifluoroethylene (TrFE).
• TrFE trifluoroethylene
• the synthesis of a block polymer comprising a PVDF block and a terpolymer block based on VDF, TrFE and 1234yf, with an iodinated or xanthate terminus, is described; as is the synthesis of a block polymer comprising a copolymer block of VDF and TrFE and a terpolymer block based on VDF, TrFE and 1234yf.
• US 8,138,274 relates to a process for preparing a crosslinked fluorinated polymer from an iodinated oligomer and a vinyl silane compound.
• the invention relates first of all to a copolymer comprising:
• polymer chains comprising units of vinylidene fluoride and tetrafluoropropene
• terminal functional groups comprising at least one alcohol, acetate, vinyl, azide, amine, acid function carboxylic acid, (meth) acrylate, epoxide, cyclocarbonate, alkoxysilane or vinyl ether.
• said polymer chains comprise units of vinylidene fluoride and 2,3,3,3-tetrafluoropropene.
• said polymer chains are statistical polymer chains.
• each said polymer chain has a number-average molecular weight of from 500 to 300,000 g / mol, preferably from 1,000 to 100,000 g / mol, and more particularly preferably from 2,000 to 50,000 g / mol. .
• the terminal functional group or groups are chosen from:
• o-Si (OR) x (CH 3) 3-x where x is an integer of 1 to 3, and each R is independently an alkyl group having 1 to 10 carbon atoms;
• the copolymer is a linear copolymer of formula (I) Rf 1 -AX, in which X is a terminal functional group, A is a said polymer chain and Rf 1 represents a halogenated end group.
• Rf 1 represents a fluorinated alkyl chain F- (CF2) 2n, n representing an integer ranging from 1 to 6.
• the copolymer is a linear copolymer of formula (II) XA-Rf 2 -A'-X, in which each X represents a said terminal functional group, A and A 'represent each a said polymer chain, and Rf 2 represents a halogenated linkage group.
• Rf 2 represents a fluorinated alkylene chain (CF2) 2n, n representing an integer from 1 to 6.
• Rf 2 represents B-Rf'-B ', with Rf' a fluorinated alkylene chain (CF2) 2n, n representing an integer ranging from 1 to 6, and B and B 'each representing a compound copolymer chain halogenated patterns.
• CF2 fluorinated alkylene chain
• B and B 'each represent a polymer chain composed of units selected from the units derived from monomers of vinylidene fluoride, trifluoroethylene, tetrafluoroethylene, 2,3,3,3-tetrafluoropropene, fluoride of vinyl, 2-chloro-1, 1-difluoroethylene, chlorofluoro-1, 1-ethylene, chlorofluoro-1,2-ethylene, chlorotrifluoroethylene of 2-bromo-1,1-difluoroethylene, hexafluoropropene, 3 3,3,3-trifluoro-2-chloropropene, 3,3,3-tetrafluoropropene, 3,3,3-trifluoro-2-bromopropene, 1H-pentafluoropropene, 3,3-trifluoropropene, 3,3,3-trifluoro-1-chloropropene, bromotrifluoroethylene and 2H-pentafluoropropene.
• B and B 'each have a number-average molecular weight of from 500 to 300,000 g / mol, preferably from 1,000 to 100,000 g / mol, and more preferably from 2,000 to 50,000 g / mol. mol.
• the copolymer is a star-shaped copolymer of formula: wherein each X represents a said terminal functional group, A, A 'and A "each represent a said polymer chain, and Rf 3 represents a halogenated linkage group.
• the copolymer is a copolymer having one of the formulas (IIIa) to (IIIh):
• n is an integer from 1 to 6 and p is an integer of 1 or 2.
• the copolymer a star-shaped copolymer of formula:
• each X represents a said terminal functional group
• A, A ', A "and A'” each represent a said polymer chain
• Rf 4 represents a halogenated linkage group
• the copolymer is a copolymer having one of the following formulas:
• the invention also relates to a process for preparing a copolymer according to the invention, comprising:
• said supplying step comprises a step of controlled radical copolymerization of a vinylidene fluoride monomer and a tetrafluoropropene monomer, in the presence of an initiator and an iodized compound as transfer agent. of chain.
• the chain transfer agent is chosen from compounds of formulas:
• CYiY 2 CY3Y4, wherein Y1, Y 2 , Ys and Y 4 are selected from H, F, Cl, Br, CF 3 , C 2 F 5 and C 3 F 7 , at least one of which is an atom of fluorine, and even more preferably a polymer chain composed of units selected from the units of vinylidene fluoride, trifluoroethylene, tetrafluoroethylene, 2,3,3,3-tetrafluoropropene, vinyl fluoride, 2-chloro, 1, 1-difluoroethylene, 2-bromo-1,1-difluoroethylene, hexafluoropropene, 3,3,3-trifluoropropene, 3,3,3-
• n represents an integer of 1 to 6 and p represents an integer of 2 or 3.
• the present invention makes it possible to meet the needs expressed above. It provides more particularly new fluorinated copolymers obtained by controlled radical copolymerization, which are functionalized and thus allow to implement subsequent reactions, for example chain extension (for block copolymers), grafting, crosslinking.
• FIG. 1 represents the 19 F NMR spectrum of an example of a di-iodinated poly (VDF-co-1234yf) copolymer according to the invention (see Example 2).
• FIG. 2 represents the IR spectrum of an example of di-iodinated poly (VDF-co-1234yf) copolymer according to the invention (see Example 2).
• the wavelength in cm -1 is represented on the abscissa, and the transmittance in% is represented on the ordinate.
• FIG. 3 represents the 1 H NMR spectrum of an example of a poly (VDF-co-1234yf) diol copolymer according to the invention (see Example 3).
• FIG. 4 shows the NMR spectrum F 19 of an example of poly (VDF-co-1234yf) diol according to the invention (see Example 3).
• FIG. 5 represents the IR spectrum of an example of a poly (VDF-co-1234yf) diol copolymer according to the invention (see Example 3). The wavelength in cm -1 is represented on the abscissa, and the transmittance in% is represented on the ordinate.
• copolymers according to the invention comprise one or more polymer chains comprising units of vinylidene fluoride (VDF) and tetrafluoropropene, having one or more functionalized terminations.
• VDF vinylidene fluoride
• unit is meant a unit resulting from the polymerization of a monomer of VDF or tetrafluoropropene respectively.
• said polymer chains consist of VDF and tetrafluoropropene units.
• at least one additional unit preferably derived from an additional hydrohaloolefin monomer, such as a hydrofluoroolefin, hydrochloro-olefin, hydrobromoolefin or hydrofluorochloroolefin monomer.
• said at least one additional unit may be chosen from units derived from trifluoroethylene, tetrafluoroethylene, vinyl fluoride, 2-chloro-1, 1-difluoroethylene, chlorofluoro-l, 1 ethylene, chlorofluoro-1,2-ethylene, chlorotrifluoroethylene, 2-bromo-1,1-difluoroethylene, hexafluoropropene, 3,3,3-trifluoropropene, 3,3,3-trifluoro-2-chloropropene 3,3,3-trifluoro-1-chloropropene, bromotrifluoroethylene, 3,3,3-trifluoro-2-bromopropene, 1H-pentafluoropropene and 2H-pentafluoropropene.
• the tetrafluoropropene units are preferably 1234yf units (that is to say from 2,3,3,3-tetrafluoropropene or 1234yf monomer). However, alternatively, it may be provided that these units are derived from one or more other isomers of tetrafluoropropene, and in particular the 1234ze (unit derived from monomer 1, 3,3,3-tetrafluoropropene or 1234ze) in the form of cis or preferably trans. Mixtures of tetrafluoropropene units from different isomers can also be used.
• copolymers according to the invention can be manufactured by a preparation process in at least two stages:
• the chain transfer agent is an iodinated compound, in which case the controlled radical copolymerization step is a ITP (lodine transfer polymerization) step, that is to say, transfer polymerization. 'iodine).
• ITP molecular transfer polymerization
• a mono-iodinated chain transfer agent is of general formula:
• FV represents a halogenated end group.
• FV is a fluorinated group.
• FV has the same meaning as above and A represents a polymer chain comprising VDF and tetrafluoropropene units, as defined above.
• Rf 1 group represents a partially or totally fluorinated alkyl chain.
• the first reaction may for example be carried out as follows: in a pressure reactor equipped with inlet and outlet valves, a pressure gauge, a stirring anchor and a rupture disk, it is possible to introduce the reagents (1- (CF2) 2n-1, tert-butanol, biscyclohexylperoxy-dicarbonate), then after 3 empty / nitrogen cycles, the reactor can be cooled to -80 ° C before transferring ethylene (in proportion equimolar with I- (CF2) 2n-1). The reaction can last 8-10 hours at 60 ° C with an increase in pressure as the reactor is heated, then a drop related to the consumption of ethylene; the di-iodinated derivative obtained can be distilled. It can be characterized by 1 H and 19 F NMR spectroscopy. This first reaction is described in detail in the article by Barthommemy et al., In Org. Lett. 1: 1689-1692 (2000).
• the first reaction is for example described in the publications of Cirkva et al., In J. Fluorine Chem., 74: 97-105 (1995), Ameduri et al., In J. Fluorine Chem., 74: 191- 197 (1995), Guyot et al. in J. Fluorine Chem., 74: 233-240 (1995) and Manseri et al. in J. Fluorine Chem., 73: 151-158 (1995).
• the second reaction may for example be carried out as follows: zinc (activated by ultrasound, or by a catalytic amount of bromine or acetic acid / acetic anhydride in methanol) may be first introduced into a flask two-pipe in which may be added dropwise the compound AcO-CH2-CHI-CH2- (CF2) 2n-1 in equimolar amount (relative to zinc) in methanol. After reaction, the reaction medium can be boiled with methanol for 4 hours.
• n 1, or 2, or 3, or 4 or 5, or 6 and A has the meaning above;
• CH 2 CH- (CF 2) 2n-Al, wherein n is 1, or 2 or 3 or 4 or 5 or 6 and A has the above meaning;
• CH 2 CH-CH 2 - (CF 2) 2n-Al, wherein n is 1, or 2 or 3 or 4 or 5 or 6 and A has the above meaning.
• n 1, or 2, or 3, or 4 or 5, or 6 and A has the meaning above;
• CH2 CH- (CF2) 2n-A-X, wherein n is 1, or 2, or 3, or 4 or 5, or 6 and A has the meaning above;
• CH2 CH-CH2- (CF 2) 2n-AX, wherein n is 1, or 2, or 3, or
• a di-iodinated chain transfer agent is of general formula:
• Rf 2 represents a halogenated linkage group.
• Rf 2 is a fluorinated group.
• Rf 2 has the same meaning as above, and A and A 'each represent a polymer chain comprising VDF and 1234 units as defined above.
• Rf 2 , A and A ' have the same meaning as above, and X represents a terminal functional group, as described in more detail below.
• the Rf 2 group represents an alkylene chain partially or fully fluorinated.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• n 1, or 2, or 3, or 4 or 5, or 6 and A and A 'have the meaning above.
• n 1, or 2, or 3, or 4 or 5, or 6 and A and A 'have the meaning above.
• n 1, or 2, or 3, or 4 or 5, or 6 and B and B 'each represents a copolymer chain composed of halogenated units (preferably B and B' having the same halogenated units).
• n 1, or 2, or 3, or 4 or 5, or 6 and A, A ', B and B' have the meaning above.
• the polymer chains B and B ' are preferably random polymer chains. They preferably each have a number-average molar mass of 500 to 300,000 g / mol, preferably from 1,000 to 100,000 g / mol and more preferably from 2,000 to 50,000 g / mol.
• a tri-iodinated chain transfer agent is of general formula:
• Rf 3 represents a halogenated linkage group.
• Rf 3 is a fluorinated, aliphatic or aromatic group.
• Rf 3 has the same meaning as above, and A, A 'and A "each represent a polymer chain comprising VDF and tetrafluoropropene units, as defined above.
• Rf 3 , A, A 'and A have the same meaning as above, and X represents a terminal functional group, as described in more detail below.
• the Rf 3 group comprises an aromatic ring of the benzene or triazine type, or an isocyanurate ring, or a phosphorus atom.
• the tri-iodinated compound is of formula:
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6 and Z is a linking group, preferably having a saturated or aromatic ring, substituted or unsubstituted, or comprising a phosphorus atom.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• This compound can be prepared in the following manner: supply of the di-iodinated compound of formula I-CH 2 -CH 2 - (CF 2) 2n-1, the preparation of which has already been described above;
• This reaction is a nucleophilic substitution of a triphenol on the compound 1-CH 2 -CH 2 - (CF 2) n-1 , which can for example be implemented as follows.
• a triphenate can first be obtained by the addition of NaH or K 2 CO 3 (in this case, the mixture is stirred under nitrogen for for example 2 hours) or sodium hydroxide on phloroglucinol; then this triphenate can be added for example dropwise at room temperature on the I-CH2-CH2- (CF2) n -l solubilized in dry methanol. After total addition, the mixture is heated at 40 ° C and then at reflux of methanol for five hours. The monitoring is performed by gas chromatography until phloroglucinol disappears. After reaction, the crude is purified by column chromatography.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• the reaction can for example be implemented as follows.
• the reaction may be a radical reaction initiated either photochemically at room temperature, or in the presence of radical initiators (azobisisobutyronitrile or AIBN type preferably at about 80 ° C, terbutyl peroxypivalate preferably at about 74 ° C, peroxypivalate of terf-amyl preferably at about 65 ° C, or bis (tert-butylcyclohexyl) peroxydicarbonate preferably at about 60 ° C, other peroxides, at temperatures at which their half-life is preferably about one hour ), or transition metal salts, or sodium dithionite / NaHCO3 / water / acetonitrile at 0 to 60 ° C (as described by Zhang et al in Chem Rev S, 41: 4536-4559, 2012).
• radical initiators azobisisobutyronitrile or AIBN type preferably at about 80 ° C, terbutyl peroxyp
• the mixture can be stirred under nitrogen for 2 hours.
• the TAC may be solubilized in previously degassed dry acetonitrile, and the di-iodinated perfluoroalkane derivative 1 (CF 2) n 1, solubilized in degassed dry acetonitrile, may be added dropwise at the required temperature.
• the reaction mixture can be stirred at the same temperature for at least 6 hours and the monitoring can be carried out by gas chromatography until the di-iodine compound disappears. After reaction, the crude may be purified by column chromatography to yield the desired derivative.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• This reaction may for example be carried out in the presence of Cu °, Fe °, CuBr, CuC; ligands such as 4'-nonafluorobutylacetophenone, 2,2'-bipyridine, N, N, N ", N", N ", N" '- hexamethyltriethylenetetramine (HMTETA), N, N, N', N ", N” -pentamethyldiethylenetriamine (PMDETA); and dimethylsulfoxide (DMSO) or ⁇ , ⁇ -dimethylformamide (DMF) as a solvent.
• ligands such as 4'-nonafluorobutylacetophenone, 2,2'-bipyridine, N, N, N ", N", N ", N" '- hexamethyltriethylenetetramine (HMTETA), N, N, N', N ", N” -pentamethyldiethylenetriamine (PMDETA); and dimethylsulfoxide (DM
• a good initial di-iodinated / triiodobenzene / ligand / metal / solvent molar ratio is approximately 1: 1.
• the temperature can be from about 50 to 140 ° C, more precisely from about 80 to 130 ° C, and the reaction time from about 12 to 24 hours.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• the reaction can for example be implemented as follows.
• the reaction may be a radical reaction initiated either photochemically at room temperature, or in the presence of free-radical initiators (of AIBN type preferably at about 80 ° C., terbutyl peroxypivalate, preferably at about 74 ° C., terp-peroxypivalate).
• the TAIC can be solubilized in acetonitrile and the di-iodine derivative 1 (CF 2) n 1 solubilized in acetonitrile is added dropwise at the required temperature.
• the reaction mixture can be stirred at the same temperature for at least 6 hours and the monitoring can be carried out by gas chromatography until the di-iodine compound disappears.
• the crude can be purified by column chromatography.
• the reaction can for example be implemented as follows.
• the reaction may be a radical reaction initiated either photochemically at room temperature, or in the presence of free-radical initiators (of AIBN type preferably at about 80 ° C., terbutyl peroxypivalate, preferably at about 74 ° C., terp-peroxypivalate). preferably at about 65 ° C or bis (tert-butyl cyclohexyl) peroxydicarbonate, preferably at about 60 ° C, other peroxides, at temperatures at which their half-life is preferably about one hour).
• free-radical initiators of AIBN type preferably at about 80 ° C., terbutyl peroxypivalate, preferably at about 74 ° C., terp-peroxypivalate.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• the first reaction may for example be implemented as follows. Propen-3-ol can be solubilized in dry acetonitrile in which NaH may be added and the mixture may be stirred under nitrogen for about 2 hours. Then 1,3,5-trifluorobenzene (in proportion 3 times smaller than propen-3-ol, solubilized in dry acetonitrile) can be added dropwise at room temperature. The reaction mixture can be heated at 40 and then 60 ° C. with stirring for at least 6 hours and the follow-up can be carried out by IR spectroscopy until the frequency of the OH vibration disappears towards 3200-3500 cm -1 .
• the second reaction consists of the radical addition of 1,6-diiodoperfluorohexane to the 1,3,5-triallyloxybenzene previously described; it may for example be a radical reaction initiated either photochemically at room temperature, or in the presence of free-radical initiators (of AIBN type preferably at about 80 ° C., tert-butyl peroxide, preferably at about 74 ° C., terf peroxypivalate. preferably at about 65 ° C or bis (tert-butylcyclohexyl) peroxydicarbonate, preferably at about 60 ° C, other peroxides preferably at temperatures at which their half-life times are about one hour).
• free-radical initiators of AIBN type preferably at about 80 ° C., tert-butyl peroxide, preferably at about 74 ° C., terf peroxypivalate. preferably at about 65 ° C or bis (tert-butylcyclohexy
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6, and p is an integer of 1 or 2.
• This compound may be prepared as follows:
• the reaction may for example be carried out using at least four times more fluorinated vinyl or allyl derivative, in the presence of AIBN preferably at about 80 ° C or terbutyl peroxypivalate preferably at about 74 ° C, or terf-amyl peroxypivalate preferably at about 65 ° C, or bis (tert-butyl cyclohexyl) peroxydicarbonate preferably at about 60 ° C, or other peroxides, preferably at temperatures at which their half-time life is about an hour.
• AIBN preferably at about 80 ° C or terbutyl peroxypivalate preferably at about 74 ° C
• terf-amyl peroxypivalate preferably at about 65 ° C
• bis (tert-butyl cyclohexyl) peroxydicarbonate preferably at about 60 ° C, or other peroxides, preferably at temperatures at which their half-time life is about an hour.
• This compound can be prepared from the corresponding tri-boro compound (in which the iodine atoms are replaced by boron atoms), which commercial product is supplied by the American company Tetramers LLC.
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, p is 1 or 2, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, p is 1 or 2, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, p is 1 or 2, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A 'and A "have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, p is 1 or 2, and
• a tetra-iodinated chain transfer agent is of general formula:
• Rf 4 represents a halogenated linkage group.
• Rf 4 is a fluorinated group.
• Rf 4 has the same meaning as above, and A, A ', A "and A'” each represent a polymer chain comprising VDF and 1234 units as defined above.
• Rf 4 , A, A ', A "and A'” have the same meaning as above, and X represents a terminal functional group, as described in more detail below.
• the tetra-iodinated compound is of formula: (IVb l S ')
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6 and Z 'is a linking group.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6 and p is an integer of 2 or 3.
• This compound may be prepared as follows:
• the first step and the second step may for example be carried out as described in the Ameduri et al. Publication, in J. Fluorine Chem., 74: 191-197 (1995).
• the first step can be carried out in the presence of FbPtCle at 80-120 ° C or terf-butyl peroxide at 130-145 ° C for at least 6 hours.
• the third step can be carried out in a basic medium, in the presence of a phase transfer catalyst of sodium tetrabutylhydrogen sulphate (TBAH) type.
• TBAH sodium tetrabutylhydrogen sulphate
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• the reaction can for example be implemented as follows.
• the reaction may be a radical reaction initiated either photochemically at room temperature, or in the presence of radical initiators (azobisisobutyronitrile type or AIBN preferably at about 80 ° C, terf-butyl peroxypivalate preferably about 74 ° C, or peroxypivalate terf-amyl preferably at about 65 ° C or bis (tert-butylcyclohexyl) peroxydicarbonate, preferably at about 60 ° C, other peroxides, at temperatures at which their half-life is preferably about one hour ).
• radical initiators azobisisobutyronitrile type or AIBN preferably at about 80 ° C, terf-butyl peroxypivalate preferably about 74 ° C, or peroxypivalate terf-amyl preferably at about 65 ° C or bis (tert-butylcyclohexyl) peroxydicarbonate, preferably at about 60
• a nitrogen or argon flask with two tubes, equipped with a refrigerant, containing HS-C2H 4 - (CF 2) 2n-1 in large excess and the C (CH 2 -O-CH 2) derivative.
• -CH CH2
• the initiator can then be added.
• the mixture can be brought to the required temperature and stirred at the same temperature for at least 6 hours.
• the excess of derivative HS-C2H 4 - (CF 2) 2n-1 can be removed by flash chromatography.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6 and p is an integer of 1 or 2.
• This compound may be prepared as follows:
• the first preparation is based on an esterification which can be catalyzed by methanesulfonic acid, for example with a Dean-Stark toluene / water system and an initial thiol / pentaerythritol molar ratio of 4-6.
• the second reaction can for example be implemented as follows.
• the reaction may be a radical reaction initiated either photochemically at room temperature or even in the presence of sunlight, or in the presence of radical initiators (azobisisobutyronitrile or AIBN type preferably at about 80 ° C, terf-butyl peroxypivalate preferably at About 74 ° C., terf-amyl peroxypivalate preferably at about 65 ° C. or bis (tert-butyl cyclohexyl) peroxydicarbonate, preferably at about 60 ° C., other peroxides, at temperatures at which their half-life times are preferably about one hour).
• radical initiators azobisisobutyronitrile or AIBN type preferably at about 80 ° C, terf-butyl peroxypivalate preferably at About 74 ° C., terf-amyl peroxypivalate preferably at about 65 ° C. or bis (tert-butyl cyclohex
• the initiator is then added.
• the mixture can be brought to the required temperature and stirred at this same temperature for at least 6 hours and the monitoring can be carried out by 1 H NMR spectroscopy until the total disappearance of the signals to 1.5 ppm attributed to the characteristic group SH of the tetrathiol . After reaction, the excess vinyl or allyl derivative can be removed by flash chromatography.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• the compound 1-CH 2 -CH 2 - (CF 2) 2n-1 can be prepared, for example, by ethylenation of 1- (CF 2) 2n-1, as described in the article by Bartheursmy et al., In Org. Lett. 1: 1689-1692 (2000).
• Pentaerythritol C (CH 2 -OH) 4 can be dissolved in dry methanol, into which either NaH or K 2 CO 3 or 40% sodium hydroxide can be added. The mixture can be stirred at room temperature for 2 hours, then a solution containing 1-CH 2 -CH 2 - (CF 2) 2n-1 dissolved in dry acetonitrile can be added dropwise.
• the initial molar ratio [1-CH 2 -CH 2 - (CF 2 ) 2n-1] o / [C (CH 2 -OH) 4 ] o may be 4-5, for example.
• n is an integer of 1 or 2 or 3 or 4 or 5 or 6.
• IA "'(CF 2 ) 2n (CH 2 ) p wherein n is an integer which is 1, or 2, or 3, or 4 or 5, or 6, p is 1 or 2, and A, A ', A "and A'" have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A ', A "and A'" have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, p is 1 or 2, and A, A ', A "and A'" have the meaning above;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A ', A "and A'" have the meaning above; -
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A ', A "and A'" have the meaning above.
• n 1, or 2, or 3, or 4 or 5, or 6, p is 1 or 2, and A, A ', A "and A'" have the above meaning, X being further defined detail below;
• n 1, or 2, or 3, or 4 or 5, or 6, and A, A ', A "and A'" have the above meaning, X being defined in more detail below.
• the controlled radical polymerization reaction is carried out starting from at least two monomers VDF and tetrafluoropropene (and optionally additional monomers if they are present), in the presence of a chain transfer agent as described above, and of an initiator.
• the initiator may be, for example, tert-butyl peroxypivalate, tere-amyl peroxypivalate, bis (4-tert-butylcyclohexyl) peroxydicarbonate, sodium, ammonium or potassium persulfates, benzoyl peroxide, terf-butyl hydroxy peroxide, terbutyl peroxide, cumyl peroxide or 2,5-bis (tert-butylperoxy) -2,5-dimethylhexane.
• the reaction is carried out in a solvent, which is for example chosen from 1, 1, 1, 3,3-pentafluorobutane, acetonitrile, methyl ethyl ketone, 2,2,2-trifluoroethanol, hexafluoroisopropanol, dimethylcarbonate, methyl acetate, ethyl acetate, cyclohexanone, water and mixtures thereof.
• a solvent which is for example chosen from 1, 1, 1, 3,3-pentafluorobutane, acetonitrile, methyl ethyl ketone, 2,2,2-trifluoroethanol, hexafluoroisopropanol, dimethylcarbonate, methyl acetate, ethyl acetate, cyclohexanone, water and mixtures thereof.
• the reaction is preferably carried out at a maximum temperature (after temperature rise) of 10 to 200 ° C, preferably 40 to 170 ° C, and a pressure of 10 to 120 bar,
• the molar ratio of the amount of initiator to the amount of monomers ranges from 0.0005 to 0.02 and preferably from 0.001 to 0.01.
• the molar ratio of the amount of chain transfer agent to the amount of monomers makes it possible to control the molar mass of the copolymer.
• this ratio is from 0.001 to 0.1, more preferably from 0.005 to 0.02.
• the initial molar ratio of the amount of the VDF monomer to the amount of the monomer (s) 1234 may be, for example, from 0.01 to 0.99, preferably from 0.05 to 0.90.
• the polymer chains obtained are of the random copolymer type.
• the number-average molar mass of each polymer chain A, A ', A ", A'” of the copolymer obtained is preferably from 700 to 400,000 g / mol, more preferably from 2,000 to 150,000 g / mol.
• the polymolecularity index of each polymer chain A, A ', A ", A'” of the copolymer obtained is preferably from 1.1 to 1.8, more preferably from 1.2 to 1.6.
• each iodinated termination at the end of a polymer chain A, A ', A ", A'” comprising VDF and tetrafluoropropene units may be converted into a terminal functional group X by a functionalization step.
• the terminal functional group X comprises an alcohol, acetate, vinyl, azide, amine, carboxylic acid, (meth) acrylate, epoxide, cyclocarbonate, alkoxysilane or vinyl ether function.
• the iodinated copolymer is reacted with allyl acetate.
• This makes it possible to convert the iodinated terminator (s) (- I) of the copolymer into -Ch-CHI-Ch -OAc terminations (OAc representing the acetate function).
• the reaction may for example be initiated with benzoyl peroxide at 90 ° C for 30 minutes to 2 hours. This reaction can be exothermic with a rise in temperature up to 170 ° C (the stoichiometry with respect to the number of iodine atoms should preferably be respected).
• the reaction may for example be carried out as follows: the copolymer may be dissolved beforehand in a solvent such as DMF or dry dimethylactamide and then added dropwise to a solution composed of activated zinc (by a few drops of bromine). or ultrasonic) and the same solvent (the molar ratio [Zinc] o / [iodoacetate copolymer] 0 being 2.5 to 4). After addition, the mixture can be brought to 80-140 ° C. for at least 3 hours and the reaction can be monitored by 1 H NMR with the disappearance of the signals to 4.5 ppm attributed to the CHI group and the presence of signals between 5 and 6.5 ppm assigned to the allylic end.
• the iodinated copolymer can be reacted with propen-3-ol.
• This makes it possible to convert the terminus (I) of the copolymer to -CH 2 -CHI-CH 2 -OH termini.
• this reaction can be carried out in the presence of AIBN with addition every 30 minutes at a temperature of 75-85 ° C.
• iodohydrin can be solubilized in a dry polar solvent and then added dropwise into a mixture of AIBN and tributyltin hydride at 10 ° C.
• the reaction mixture can be brought to room temperature for one hour and then at 40 ° C and finally 60 ° C for at least 3 hours and the reaction can be monitored by 1 H NMR with the disappearance of the signals to 4.5 ppm assigned to the CHI group and the presence of the signal to 1. 8 ppm assigned to the central CH of the CH2CH2CH2OH end.
• the iodinated copolymer can be reacted with ethylene. This makes it possible to convert the terminus (I) of the copolymer into -CH 2 -CH 2 -I termini.
• the reaction may for example be implemented as follows.
• the reagents (copolymer, tert-butanol, bis (terf-peroxydicarbonate) butyl cyclohexyl)) can be introduced, then after 3 cycles under vacuum / nitrogen, the reactor is cooled to -80 ° C before transferring ethylene (in equimolar proportion with the iodinated functions of the copolymer).
• tert-butyl peroxypivalate may also be used as an initiator at about 74 ° C or terf-amyl peroxypivalate at about 65 ° C.
• azide termini -CH 2 -CH 2 -N 3 can in turn be converted into amino termini -CH 2 -CH 2 -NH 2 by reaction with hydrazine;
• the conversion reaction to alcohol endings may for example be implemented as follows.
• the poly (VDF-co-1234) bis (ethylenated) copolymer can be dissolved in DMF. Water can be added and bubbled with nitrogen for 30 minutes.
• the reaction mixture can be heated to 100-110 ° C with stirring for at least 12 hours.
• the reaction crude can be cooled to room temperature and a mixture of H 2 SO 4 (25 g) in methanol (70 g) can be added dropwise. This mixture can be stirred at room temperature for 24 hours. Then the gross
• the reaction mixture can be washed with distilled water (3 ⁇ 100 ml), a solution of Na 2 S 2 O 5 and ethyl acetate (200 ml).
• the organic phase can be dried over MgSO 4 and sintered.
• the ethyl acetate and traces of DMF can be removed by rotary evaporation (40 ° C / 20 mm Hg).
• the viscous oil or solid, depending on the proportions of VDF in the poly (VDF-co-1234) copolymer, can be dried at 40 ° C under 0.01 mbar to constant weight.
• the copolymer can thus be obtained in a yield of about 65-80% and characterized by 1 H NMR and 19 F.
• the conversion reaction to acrylate termini can be implemented, for example, as follows.
• the copolymer can be dissolved in dry THF and stirred with poly (4-vinylpyridine).
• the reaction mixture can be cooled to 0 ° C and saturated with nitrogen (by bubbling and holding under a stream of nitrogen) and 20 mg of hydroquinone can be added thereto.
• An excess of acryloyl chloride (about 3 times relative to the OH ends) can be added to the syringe through a septum in four doses over a 4 hour interval.
• the reaction mixture can be heated to 40 ° C.
• poly (4-vinylpyridine) can be removed by filtration.
• the conversion reaction to methacrylate termini can be carried out as the previous reaction, using either methacryloyl chloride or methacrylic anhydride as reagent.
• the yield can vary from 65 to 85%.
• the conversion reaction to azide termini can be implemented, for example, as follows.
• the copolymer in a schenk tube, can be solubilized in a mixture of DMSO and water (in a volume ratio of DMSO / water of about 25) and then stirred with an excess of sodium azide (in a ratio of ).
• the solution may be stirred at 50 ° C for 48 hours.
• the crude reaction product After having returned to room temperature, the crude reaction product can be poured into a large excess of water and then extracted with a mixture of diethyl ether / dimethyl carbonate. This protocol can be repeated twice.
• the organic phase can be washed twice with water, 10% sulphite sodium (2 times), water (3 times), sodium hydroxide, and finally dried over MgSO 4 , and filtered.
• the solvent can be evaporated under reduced pressure and lead to a greenish product with an azide-terminated copolymer yield ranging from 60 to 75%.
• the conversion reaction to carboxylic acid terminations may for example be carried out as follows.
• the copolymer can be solubilized in a mixture of acetone (7 parts) and diethyl ether (3 parts).
• Jones catalyst (composed of 25 ml of pure sulfuric acid in a mixture of 25 g of chromium oxide and 70 ml of water) can be added dropwise at room temperature until a brown-orange color becomes persistent.
• the crude reaction product can be treated with two washings with water and the fluorinated organic phase can then be extracted with diethyl ether, dried over MgSO 4 , filtered and concentrated. If the VDF content is greater than 85 mol%, the solid product can be purified by precipitation in cold pentane.
• the acid terminated copolymer can be characterized by 1 H NMR spectroscopy (showing the absence of center signal at 3.8 ppm attributed to methylene groups CH 2 OH). The yield can be about 60 to 75%.
• the iodinated copolymer can be reacted with allyl glycidyl ether by photochemical initiation or in the presence of radical initiators mentioned above.
• the reaction can for example be implemented as follows. An excess of allyl glycidyl ether (depending on the number of iodine atoms) can be stirred in the presence of benzoyl peroxide and the iodinated copolymer at 90 ° C for 30 minutes to 3 hours. The resulting Iodoepoxide -CF2-CH2CHICH2OCH2-epoxide end copolymer is obtained in a yield of 80-85%.
• This reaction can be exothermic with a rise in temperature up to 170 ° C if the initiator addition is carried out at 90 ° C.
• the reduction of the iodine atoms can be carried out in the presence of SnBusH and AIBN as previously described for obtaining the alcohol endings.
• a carbonation of the epoxy endings can be carried out, so as to convert the -O-CH 2 -terminals.
• the reaction can for example be implemented as follows.
• the copolymer can be filtered.
• contents in units 1234 greater than 20% amorphous waxes sticking to the walls of the Erlenmeyer flask can generally be obtained.
• the excess of pentane can be removed and the wall-bonding copolymer can be solubilized in acetone and then re-precipitated in an excess of pentane, dried to constant weight and finally characterized by 1 H NMR and 19 F NMR. .
• This conversion can for example be implemented as follows. Palladium acetate and 1,10-phenanthroline (in slight excess) can be dissolved separately in dichloromethane and mixed in a Schlenk tube at 20 ° C for 15 minutes. This solution, the alcohol-terminated poly (VDF-co-1234) copolymer described above and a large excess of vinyloxyethane (or ethyl vinyl ether, 20 times more) can be placed in a pressurized reactor. This autoclave can be closed and the reaction mixture heated with stirring at 60 ° C for 48 hours. Volatile reagents can be removed on a rotary evaporator.
• the alcohol endings described above are converted into alkoxysilane endings, for example trialkoxysilane endings (for example tri (m) ethoxysilanes) or dialkoxymethylsilane (for example di (m) ethoxymethylsilane), or alkoxydimethylsilanes (for example ( m) éthoxydiméthylsilane).
• trialkoxysilane endings for example tri (m) ethoxysilanes
• dialkoxymethylsilane for example di (m) ethoxymethylsilane
• alkoxydimethylsilanes for example ( m) éthoxydiméthylsilane
• This conversion can for example be implemented as follows.
• An excess of vinyl thalkoxysilane (or vinyl dialkoxymethylsilane or vinyl alkoxydimethylsilane) such as vinyl triethoxysilane (or vinyl diethoxymethylsilane or vinyl ethoxydimethylsilane) can be stirred in the presence of benzoyl peroxide and iodinated copolymer at 90 ° C or peroxypivalate. tert-butyl preferably at about 74 ° C for 1 to 5 hours.
• the excess can be adjusted according to the number of iodine atoms: for example an excess of 3 for 2 iodine atoms, 4 for 2 iodine atoms and 5-6 for 4 iodine atoms).
• This reaction can be exothermic with a rise in temperature up to 170 ° C if the initiator addition is carried out at 90 ° C.
• Preferred terminal functional groups are therefore the following groups:
• copolymers according to the invention thanks to their terminal functions, make it possible to manufacture more complex polymers of higher molar mass, or crosslinked networks.
• acrylate or methacrylate terminations make it possible to manufacture crosslinked copolymers by exposing the copolymers of the invention to free radicals.
• the source of free radicals may be, for example, a photoinitiator (initiator sensitive to UV radiation) or the thermal decomposition of an organic peroxide.
• photoinitiators are the compounds Darocur® 1,173, Irgacure® 819 and Irgacure® 807 from Ciba Specialty Chemicals.
• T-butyl peroxypivalate is an example of a suitable organic peroxide.
• copolymers of the invention the source of free radicals and optionally fillers (carbon black, fluoropolymer powders, mineral fillers, etc.), dyes and other adjuvants may be mixed, and the crosslinking initiated by exposure to radiation UV or heat, as appropriate.
• fillers carbon black, fluoropolymer powders, mineral fillers, etc.
• dyes and other adjuvants may be mixed, and the crosslinking initiated by exposure to radiation UV or heat, as appropriate.
• copolymers according to the invention with amino terminations can be used to manufacture 1) polyamides, in a manner known per se, or 2) polyurethanes from telechelic products. bis (cyclocarbonate) (and preferably with respect to isocyanate reactants), or 3) epoxy resins.
• the azide-terminated copolymers according to the invention can be used to carry out polycondensation, crosslinking or polyaddition reactions with alkynes or cyano derivatives.
• copolymers according to the invention with triaikoxysilane endings can be used to carry out crosslinking reactions by a sol-gel process via an acid activation (hydrochloric acid, sulfonic acid or methanesulfonic acid type).
• TPPI Terf-butyl peroxypivalate
• tert-amyl peroxypivalate bis (tert-butylcyclohexyl) peroxydicarbonate: Akzo Nobel (Compiègne, France);
• C6F13I 1-iodoperfluorohexane (C6F13I) (purity of 99%): Elf Atochem; the product is treated with sodium thiosulfate, dried over magnesium sulfate and distilled before use;
• potassium persulfate K2S2O8 (99% purity), allyl alcohol, tributyltin hydride (BusSnH), azobisisobutyronitrile (AIBN), dimethyl carbonate (DMC), pentane, acetone (analytical grade), acetonitrile (analytical grade), methanol (grade) analytical), methyl ethyl ketone (MEK), tetrahydrofuran (THF, analytical grade) and calcium hydride (99% powder): Sigma-Aldrich (Saint Quentin-Fallavier, France);
• NMR specttra are recorded on a Bruker AC 400 instrument. Deuterated chloroform, d6-N, N-dimethylsulfoxide and d6-acetone are used as solvents. Tetramethylsilane (TMS) or CFCI3 are used as references for 1 H and 19 F nuclei. Coupling constants and chemical shifts are given in Hz and ppm, respectively.
• the experimental conditions for the recording of the 1 H and 13 C spectra are as follows: tilt angle of 90 ° (resp 30 °), acquisition time of 4.5 s (respectively 0.7 s) ), pulse delay of 2 s (respectively 2 s), number of scans of 128 (respectively 512), and pulse width of 5 s for 19 F NMR.
• Size Exclusion Chromatography size exclusion chromatograms (SEC) or gel permeation chromatograms (GPC) are obtained with Agilent Technologies multi-sensing GPC 50 instrument with its software (Cirrus). Two PL1 1 13-6300 ResiPore 300 x 7.5 mm columns (200 ⁇ Mw ⁇ 20,000,000 gmol-1) were used with THF as eluent, with a flow rate of 1.0 mL.min -1 at room temperature. Viscosimetric capillary detectors (PL0390-06034) with refractive index (390-LC PL0390-0601) and light scattering (PL0390-0605390 LC with 2 scattering angles: 15 ° and 90 °) were used. Calibration is carried out either with polystyrene or with polymethyl methacrylate (PMMA) standards if the copolymers contain a high proportion of VDF and in the latter case the eluent used is DMF. 1% by mass.
• Thermogravimetric Analysis is performed on a T Instruments instrument 105 51 from TA Instruments, in air, with a heating rate of 10 ° C.nnin ⁇ 1 from room temperature to a maximum of 550 ° C .
• the sample mass is 10 to 15 mg.
• Differential Scanning Calorimetry Differential scanning calorimetry (DSC) analyzes are performed on a Netzsch 200F3 instrument equipped with Proteus software under a nitrogen atmosphere with a heating rate of 20 ° C / min. The temperature range is -50 to + 200 ° C. The system is temperature calibrated using indium and n-hexane. The sample mass is about 10 mg. The second pass leads to a glass transition temperature defined as the point of inflection in the increase in heat capacity while the melting temperature is determined by the maximum of the exothermic signal.
• the autoclave Before the reaction, the autoclave is pressurized with 30 bar of nitrogen to check for possible leaks. The autoclave is then vacuum conditioned (10 -2 mbar) for 40 minutes to remove all traces of oxygen. The liquid phases (with dissolved solids) are introduced by a funnel, then the gases (1234 yf and then VDF) are transferred with double weighing (measurement of the difference in weight before and after the introduction of the gases in the autoclave). The reaction mixture is then mechanically stirred and heated at 74 ° C or 80 ° C for at least 4-6 hours.
• the autoclave is cooled in ice and degassed to release the unreacted gases.
• the product is dissolved in acetone, concentrated with a rotary evaporator, precipitated in cold pentane (or water) and filtered. If necessary, a second precipitation is performed.
• the product is then dried under vacuum (10 mbar) at 60 ° C for 12 hours to constant weight and is characterized by SEC and 1 H NMR spectroscopy and 19 F.
• the autoclave After 14 hours of reaction, the autoclave is placed in an ice bath for about 60 minutes, and unreacted VDF and 1234yf are released. After opening the autoclave, the product is extracted with MEK and then precipitated in ice cold pentane, filtered and dried under vacuum. A white powder (20.7 g) is obtained with a yield of 78-80%.
• the poly (VDF-co-1234yf) copolymer is soluble in various polar solvents, such as acetone, DMF, THF, MEK, and DMSO.
• TBPPI is used instead of K2S2O8 as a starter, and the concentrations of VDF, 1234yf, initiator and iodinated agent are modified.
• the composition of the copolymer is determined by NMR, the molar mass is determined by SEC calibrated with PS or PMMA (which also makes it possible to determine the polymolecularity index), the degradation temperature (10% ) is determined by TGA in air at 10 ° C / min, and the glass transition, melting and crystallization temperatures are determined by DSC.
• the 19 F NMR spectrum of the copolymer of the test 5 is illustrated in FIG. 1.
• the IR spectrum of this copolymer is illustrated in FIG.
• Example 3 Preparation of Functionalized P (VDF-Co-1234vf) Functionalized bis (iodohydrin)
• the poly (VDF-co-1234yf) oligomer was introduced.
• di-iodine of Example 2 5.0 g, 8.0 mmol
• allyl alcohol 2.78 g, 47.8 mmol
• dry acetonitrile 50 mL
• the flask is heated to 80 ° C.
• AIBN 0.262 g, 1.6 mmol
• the reaction is carried out under a nitrogen atmosphere at 80 ° C for about 20 h. After cooling to room temperature, the reaction mixture is filtered with cotton, and the excess solvent is removed by rotary evaporator (40 ° C / 20 mmHg). A yellowish viscous liquid is obtained which is dried (40 ° C / 0.01 mbar) to constant weight.
• the poly (VDF-co-1234yf) telechelic bis (iodohydrin) copolymer is obtained with a yield of 90%.
• the mixture is kept at 4 ° C for 12 h, then the pentane is decanted from the precipitate. The remaining solvent is evaporated under vacuum and the yellowish viscous liquid obtained is dried (40 ° C / 0.01 mbar) to constant weight. The product is obtained with an overall yield of 82%.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• General Chemical & Material Sciences (AREA)
• Inorganic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Graft Or Block Polymers (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=55299622

Family Applications (1)

Country Status (7)

Families Citing this family (5)

Family Cites Families (11)

• 2015
  • 2015-10-19 FR FR1559945A patent/FR3042502B1/fr not_active Expired - Fee Related
• 2016
  • 2016-10-18 JP JP2018538953A patent/JP2018530662A/ja not_active Withdrawn
  • 2016-10-18 CN CN201680060954.9A patent/CN108137724A/zh active Pending
  • 2016-10-18 WO PCT/FR2016/052686 patent/WO2017068276A1/fr active Application Filing
  • 2016-10-18 EP EP16798242.0A patent/EP3365377A1/fr not_active Withdrawn
  • 2016-10-18 US US15/769,263 patent/US20180305483A1/en not_active Abandoned
  • 2016-10-18 KR KR1020187011815A patent/KR20180068991A/ko unknown

Also Published As

Similar Documents

Legal Events