Abstract
A one-pot multistep growth melt procedure utilizing multistep feeding has been developed to enable the synthesis of thermoplastic polymers based on 4-hydroxybenzoic acid (HBA) and 6-hydroxy-2-naphthoic acid (HNA)with greater numbers of alternating units in their backbone chains. The decreased melting point (Tm) and glass transition temperature (Tg) indicated that the multistep feeding procedure helped to enhance the flexibility of the backbone chain due to the increasing number of alternating blocks, due to a reduction in the stacking between different main-chains, thus enabling the formation of liquid crystalline polyester (LCP) fibers with oriented structures. The covalent incorporation of rigid cage-like silsesquioxane groups led to a significant reduction of the melting point, resulting from the inevitable transformation of the original symmetrical backbone structure to a less ordered structure, due to the steric effect and hybrid feature of silsesquioxane. The presentation of silsesquioxane groups also enhanced the aggregation of ultrafine fibers with well-aligned orientation in the molten state and produce stronger fiber bundles.
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