Synthesis of 4-Chloro-1,3-Diazobenzene Bent-Cores Liquid Crystals and Characterizations of Their Mesogenic Behaviors and Photoisomerization Phenomena

<p></p><p>Azobenzene-based bent-core liquid crystals demonstrate a variety of mesomorphic behaviors and photochromic properties which are desirable for optical switching. Nowadays azobenzene-based bent-core liquid crystal (ABLC) compounds usually exhibit at least one of the following traits which are unfavorable for practical applications: (1) narrow temperature windows of nematic phases, (2) high phase transition temperature, and (3) long period of light stimulation to reach photostationary states. In this study, a series of ABLC compounds <b>4a–4g</b> were synthesized by adding azo functional groups and chlorine substituent to the central bent-cores to form 4-chloro-1,3-dizaophenylene bent-cores. These ABLC compounds were characterized by i. fourier-transform infrared spectroscopy (FTIR), ¹H and ¹³C nuclear magnetic resonance (NMR), and mass spectrometry (MS) for their structures, ii. differential scanning calorimetry (DSC) and polarized optical microscopy (POM) for their mesogenic properties, and iii. ultraviolet–visible spectroscopy (UV-Vis) and POM for their photosensitivity. The experimental results show that all compounds exhibited broad temperature windows of mesogenic phases. In particular, compound <b>4c</b> showed a broad temperature window of 63.8 °C for nematic phase. Molecular simulations indicate that the molecular dipole moments of compounds <b>4a–4g</b> are closely associated with the temperatures of Sm – N phase transition and temperature ranges of nematic phases. In addition, simulation results reveal that the terminal alkyl chains exhibit a diphasic effect on the molecular polarity: extending the terminal chain can initially reduce and then increase the molecular dipole moments due to the severe structural disorder of overly extended terminal chain. These findings indicate that the intermolecular forces play a vital role in shaping the mesogenic behavior of ABLCs. Comprehensive characterizations of photochromatic properties show that <b>4c</b> was highly photosensitive and displayed rapid photoisomerization processes. At room temperature, compound <b>4c </b>dissolved in ethyl acetate solution can reach photostationary state in 10 seconds. At 95 °C, compound <b>4c</b> in nematic phase became isotropic liquid under UV-irradiation in 3 seconds due to the forward <i>trans – cis</i> photoisomerization and can be restored to be nematic under natural visible light in 5 seconds because of the backward <i>cis – trans</i> photoisomerization. This study linking the mechanistic details with mesogenic properties provides valuable insights to improve future design of azobenzene bent-core liquid crystals for practical applications especially in photonic applications.</p><p><br></p><p>Pertinent molecular structure files (mol2) can be downloaded from</p><p><a href="https://github.com/er1czz/ABLC">https://github.com/er1czz/ABLC</a><br></p><p></p>