RAFT synthesis of well-defined PVDF-b-PVAc block copolymers
Résumé
RAFT polymerization of vinylidene fluoride (VDF), leading to relatively well defined poly(vinylidene
fluoride) (PVDF), is negatively affected by chain inversion resulting in less easily reactivatable PVDFT-XA
dormant chains (terminated with the tail end of an inversely added VDF unit; XA = xanthate moiety).
Although slow reactivation of these chains by PVDF• radicals (in contrast to general belief) was recently
demonstrated, slow radical exchange leads to progressive loss of chain growth control. This article deals
with the possibility of synthesizing block copolymers from PVDF-XA macroCTAs by sequential addition.
The investigations show that only PVDFH-XA (chains terminated with the head end of regularly added
VDF) can be reactivated by PNVP• (poly(N-vinylpyrrolidone)) radicals and that PVDFT-XA chains are completely
unreactive in the presence of PNVP•, PB• (poly(butylacrylate)) or PDM• (poly(N,N’-dimethylacrylamide)).
However, both PVDFH-XA and PVDFT-XA can be reactivated by PVAc• (poly(vinyl acetate))
radicals. The reactivation of the PVDFT-XA, albeit slower than that of the PVDFH-XA, is sufficiently fast to
allow the synthesis of unprecedented well-defined PVDF-b-PVAc block copolymers with relatively high
end-group fidelity. DFT calculations rationalize this behavior on the basis of faster radical exchange in the
order PVDFH-XA/VAc > PVDFH-XA/NVP > PVDFT-XA/VAc ≫ PVDFT-XA/NVP. The success of the chain
extension also relies on faster activation relative to homopropagation of the chain extending monomer, as
well as fast addition of the released PVDF•
H and PVDF•
T to the monomer.
Domaines
Polymères
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