2002•Polymer InternationalRequires access

Photoinitiated alternating copolymerization of vinyl ethers with chlorotrifluoroethylene

Manuel Gaboyard, Yves Hervaud, Bernard Boutevin

Open publisher page 31 citations

Abstract

Abstract The photoinitiated copolymerization of chlorotrifluoroethylene (CTFE) with several vinyl ethers [ethyl vinyl ether (EVE), 2‐chloroethyl vinyl ether (CEVE), cyclohexyl vinyl ether (CHVE), 4‐hydroxybutyl vinyl ether (HBVE)] was studied. CTFE is an acceptor monomer (e ∼ 1.5) whereas vinyl ethers are donor monomers (e ∼ −1.5), and therefore their copolymerization led to alternating copolymers, as indicated by elementary analysis. The equilibrium constant (KF) of the charge‐transfer complex formation (CTC) was determined by 19F NMR spectroscopy. Under our experimental conditions, KF was low for CHVE/CTFE and HBVE/CTFE systems, 0.058 and 0.013 l mol−1 respectively. It can be assumed that the copolymerization involves the free monomers rather than propagation via the donor–acceptor complex. The alternating structure arises from the great difference in polarity between the two types of monomers. Several functional copolymers were prepared in good yield and with molecular weight close to 15 000 g mol−1. © 2002 Society of Chemical Industry

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What this paper is about

Abstract The photoinitiated copolymerization of chlorotrifluoroethylene (CTFE) with several vinyl ethers [ethyl vinyl ether (EVE), 2‐chloroethyl vinyl ether (CEVE), cyclohexyl vinyl ether (CHVE), 4‐hydroxybutyl vinyl ether (HBVE)] was studied. CTFE is an acceptor monomer (e ∼ 1.5) whereas vinyl ethers are donor monomers (e ∼ −1.5), and therefore their copolymerization led to alternating copolymers, as indicated by elementary analysis. The equilibrium constant (KF) of the charge‐transfer complex formation (CTC) was determined by 19F NMR spectroscopy. Under our experimental conditions, KF was low for CHVE/CTFE and HBVE/CTFE systems, 0.058 and 0.013 l mol−1 respectively. It can be assumed that the copolymerization involves the free monomers rather than propagation via the donor–acceptor complex. The alternating structure arises from the great difference in polarity between the two types of monomers. Several functional copolymers were prepared in good yield and with molecular weight close to 15 000 g mol−1. © 2002 Society of Chemical Industry

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Available abstract

Abstract The photoinitiated copolymerization of chlorotrifluoroethylene (CTFE) with several vinyl ethers [ethyl vinyl ether (EVE), 2‐chloroethyl vinyl ether (CEVE), cyclohexyl vinyl ether (CHVE), 4‐hydroxybutyl vinyl ether (HBVE)] was studied. CTFE is an acceptor monomer (e ∼ 1.5) whereas vinyl ethers are donor monomers (e ∼ −1.5), and therefore their copolymerization led to alternating copolymers, as indicated by elementary analysis. The equilibrium constant (KF) of the charge‐transfer complex formation (CTC) was determined by 19F NMR spectroscopy. Under our experimental conditions, KF was low for CHVE/CTFE and HBVE/CTFE systems, 0.058 and 0.013 l mol−1 respectively. It can be assumed that the copolymerization involves the free monomers rather than propagation via the donor–acceptor complex. The alternating structure arises from the great difference in polarity between the two types of monomers. Several functional copolymers were prepared in good yield and with molecular weight close to 15 000 g mol−1. © 2002 Society of Chemical Industry

Key concepts: Chlorotrifluoroethylene, Copolymer, Vinyl ether, Monomer, Polymer chemistry, Vinyl polymer, Ether, Chemistry

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