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Even though we fully understood that such an optically active helical polymer leads to a further macroscopic chirality in the liquid crystal state, it seemed to be appropriate to conduct the research with PDMB because this polymer is very stiff and its liquid crystalline phase behavior is well understood.3
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The molecular weights of the samples used for the AFM observations were much higher than those used in the SR-SAXS measurements because the bandings observed in the samples with the molecular weight of 10- 30k were too narrow and barely recognizable by our AFM apparatus
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