Abstract

Nylons 8 10 and 10 12 have been synthesized and crystallized as chain-folded lamellae from 1,4-butanediol and the results compared with previous studies on Nylons 4 6 and 6 8. In 2N 2(N + 1) Nylons, the lengths of the two alkane segments are equal and two different hydrogen-bonded sheet schemes are possible: progressive or alternating shear. At room temperature, Nylons 8 10 and 10 12 adopt the progressive scheme and the adjacent re-entry folds in the crystals must be in the alkane chain segments. In contrast, Nylons 4 6 and 6 8 lamellae, crystallized from the same solvent, exhibit the alternating hydrogen bonding scheme and each adjacent re-entry fold must contain an amide group. The transition in the chemical nature of the lamellar surface, from the amide fold to the alkane fold, occurs in passing from Nylon 6 8 to 8 10. Thus, the progressive hydrogen-bonded sheet/alkane fold structure is energetically more favorable, provided the alkane-folding geometry is sufficiently relaxed; this comes with increasi...

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