Evidence for complexation-induced micro-extension of poly(vinyl alcohol) chains in interphase and amorphous domains from solid-state NMR

The three-phase structure of poly(vinyl alcohol) (PVA)-iodine complexes was elucidated by solid-state NMR (SSNMR), of which the micro-extension of the PVA segment in the interphase and amorphous domains was directly confirmed. The three-phase structure of the PVA-iodine complex was decomposed by the inverse C-13 T-1-filter, where C-13 NMR resonance lines of a C(H) triplet were observed in all three phases. The chain axis of similar to 26% extended chains in the interphase deviates 35 degrees-50 degrees relative to the stretching direction, while there is only a 1 degrees deviation for the extended chains in the crystalline domain. The increasing iodine concentration results in the increment of hydrogen-bonded C(H) fractions in both the amorphous and interphase domains, while the distribution of different C(H) fractions remains almost constant in the crystalline domain. Such an increment results from the locally extended PVA chains induced by polyiodine species (I-3(-)/I-5(-)), since the hydrogen bond(s) (HBs) required a specific direction. Direct evidence for this comes from the similar C-13 CP/MAS spectra of C(H) in the three phases between unoriented iodine-doped PVA and highly oriented pure PVA. This supports the aggregation model for the formation mechanism of PVA-iodine complexes, where the PVA chain takes an extended zig-zag conformation.

Automated summary

The three-phase structure of poly(vinyl alcohol) (PVA)-iodine complexes was studied using solid-state NMR. The micro-extension of the PVA segment in the interphase and amorphous domains was confirmed, and it was found that the increasing iodine concentration led to an increment in the hydrogen-bonded C(H) fractions in both the amorphous and interphase domains. The results provide evidence for the aggregation model for the formation mechanism of PVA-iodine complexes.