Dialkoxy derivatives of anthraquinone (AQ), dicyano-anthraquinone (DCAQ) and tetracyanoanthraquinone (TCAQ) were synthesized and their associated electrochemical, optical and self-assembling properties were investigated as candidates for n-type materials. AQ shows UV absorption features, whereas both DCAQ and TCAQ exhibit bathochromic and hyperchromic electronic transitions into the visible region. The electron accepting strength of the three compounds was established by cyclic voltammetry as -1.52 V, -1.3 V and -0.9 V vs. ferrocene/ferricenium for AQ, DCAQ and TCAQ, respectively. All three quinones displayed quasireversible, two sequential one-electron transfer redox reactions. DFT calculations of DCAQ and TCAQ demonstrate structural changes upon reduction, which is supported by spectroelectrochemical experiments. Furthermore, the structural changes result in different absorption profiles and show potential as electrochromic materials. Finally, both AQ and DCAQ show liquid crystalline phases and importantly, DCAQ exhibits both a smectic liquid crystalline and a soft crystal phase between -6 °C and 85 °C, which offers promise as a self-assembling n-type material.

The syntheses of six room-temperature discotic liquid crystals based on an alkoxy-anthraquinone (AQ) framework is described. Differential scanning calorimetry, X-ray diffraction (XRD), and cross-polarized microscopy were used to identify phases and confirm phase-transition temperatures. Cross-polarized microscopy results suggest columnar discotic structures at room temperature. However, the AQ derivatives also undergo mesophase-to-mesophase transitions, which are attributed to rectangular- to hexagonal-columnar discotic transitions based on XRD analysis. Furthermore, some of the compounds display remarkable liquid crystalline phase stability that spans from -50 to 150 degrees C, a useful temperature range for organic materials applications. The different AQ derivatives did not exhibit electronic perturbations, as all compounds have absorption onsets of approximately 400 nm. Finally, solution cyclic voltammetry of the AQ derivatives was carried out to determine the redox potentials, diffusion coefficients, and electron transfer rate constants. All AQ derivatives had E(1/2) values that ranged between -1.52 and -1.70 V vs Fc/Fc(+). Diffusion coefficients and electron transfer rates for all AQ derivatives ranged between 0.4 and 7.1 x 10(-6) cm(2) x s(-1) and 0.9 and 5.2 x 10(-3) cm x s(-1), respectively.