“…For example, p -substitution of azobenzene with functional groups including F, Cl, Br, I, CN, and NO 2 result in the formation of solid phase for both E and Z isomers, due to the facile crystallization of twisted Z structures. Out of a large series of arylazopyrazole derivatives p -substituted on the aryl ring with various alkoxy groups (OC n H 2 n +1 and OC n H 2 n –1 ; n = 1–12), only one compound (OC 8 H 15 ) displays a liquid phase as Z isomer (i.e., melting point below room temperature), while the rest of the compounds with shorter or longer chains are solids as both E and Z isomers. The phase of Z isomer is also impacted by the o -substituents on azobenzene core; for example, azobenzenes o -substituted with halides (F and Cl) undergo solid–liquid phase transition, while the o -MeO-substituted azobenzene exhibits solid phases for both E and Z , despite bearing an identical p -tridecanoate group.…”