The polymorphism of poly(vinylidene fluoride). I. The effect of head-to-head structure

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Abstract
The phenomenon of polymorphism in poly(vinylidene fluoride) has been observed recently by several authors. It has also been reported that high-resolution NMR measurements demonstrate the presence in this polymer of head-to-head linkages, resulting from the “backward” addition of from 5-6% of the monomer units. Since the van der Waals radii of fluorine (1.35 Å) and hydrogen (1.1-1.2 Å) are similar, the cocrystallization in a polymer chain of units that differ only by the substitution of fluorine atoms for hydrogen atoms is not unexpected. The two polymorphic forms of poly(vinylidene fluoride), examined in this investigation, have different chain conformations. Chains in phase I have a planar zigzag conformation, while chains in phase II are assumed to exhibit a 21 helical conformation. The incorporation into the polymer chain of small amounts of tetrafluoroethylene or trifluoroethylene comonomer favored the crystallization of phase I. This is in accord with the relative abilities, deduced from consideration of atomic size, of these comonomers to cocrystallize with vinylidene fluoride units in the two indicated chain conformations of the polymer. Since tetrafluoroethylene units are present in the head-to-head structure in the homopolymer, it can be concluded that the elimination of the head-to-head structure will eliminate or restrict crystallization in phase I.

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