Abstract
Dimeric hydrazide derivatives with nitro, phenyl, and methyl terminal subsistents were synthesized. The liquid crystalline properties were investigated by differential scanning calorimetry, polarizing optical microscopy and wide angle X‐ray diffraction. Interestingly, intercalated smectic phases were observed in these symmetric liquid crystal dimers. The effect of the substituents and the length of the spacer on the mesophase is discussed, confirming that intermolecular hydrogen bonding between the hydrazide groups was the driving force for the formation of the intercalated structures.
Acknowledgements
The authors are grateful to the National Science Foundation Committee of China (project No. 50373016), Program for New Century Excellent Talents in Universities of China Ministry of Education, Special Foundation for PhD Program in Universities of China, Ministry of Education (Project No. 20050183057), and Project 985‐Automotive Engineering of Jilin University for their financial support of this work.