Non-classical temperature-dependent phase sequence: long-lived metastable piezoelectric helical columnar liquid crystalline polymorph

Polymorphism is an intriguing research topic, because multiple functionalities can be accessed from a single material. Herein, we report the unusual polymorphic behavior of a liquid crystalline (LC) naphthalene derivative (1) based on 1,2,3-triazolyl linkages. Two individual polymorphs corresponding to metastable helical columnar (Col(hel)) LC and thermodynamically stable monoclinic crystalline (Cry) phases can be obtained at room temperature by mild thermal treatments. According to the thermal, dynamic, and structural analyses of 1, the triazolyl H-bonded network along the columnar axis plays a key role in the formation of the polar helical columnar order and its longevity. As a consequence of the remarkable stability of the metastable Col(hel), a non-classical phase sequence, that is, Col(hel)-liquid-cry-liquid upon heating, was observed for the first time, although it was also predicted theoretically in monotropic LC polymorphism. Interestingly, piezoelectric measurement of the poled Col(hel) polymorph showed a noticeable increase in open-circuit voltage upon the application of force, which was more than five times greater than the measured voltage of the Cry polymorph.

Automated summary

The study of a liquid crystalline naphthalene derivative unveiled its unusual polymorphic behavior, leading to the formation of polar helical columnar structures and influencing thermal stability. Additionally, the poled Col(hel) polymorph exhibited a significant increase in open-circuit voltage under force application, surpassing the Cry polymorph by more than five times.