Photochemical behaviour and toxicity evolution of phenylbenzoate liquid crystal monomers in water

Liquid crystal monomers (LCMs) are a group of emerging pollutants that pose potential environmental risks because of their ubiquitous occurrence and toxicity. Understanding their environmental transformation is essential for assessing the ecological risk. In this study, we investigated the photochemical transformation kinetics, mechanism, and photo-induced toxicity of three phenylbenzoate LCMs in water. Their apparent photolytic rate constants were within (0.023 - 0.058) min(-1), and the half-lives were < 30.0 min, showing lower persistence in water. Dissolved organic matter significantly inhibited their photolysis because of light-shielding effect and quenching of excited triplet states of LCMs. Their photolysis mainly occurred through excited triplet states, and the reactive oxygen species (i.e., & sdot;OH, O-1(2) and & sdot;O-2-) contributed to their degradation. The main photolysis pathways were ester bond cleavage, & sdot;OH substitution/addition, and defluorination. Experiments and computational simulation revealed that some <middle dot>OH addition/substitution products have similar toxicity with LCMs. Additionally, the center dot OH reaction rate constants (k(OH)) of LCMs were determined to be > 1 x 10(9) M-1 s(-1), evidence for their high reactivity toward & sdot;OH. We have further developed reliable methods to estimate k(OH) of other phenylbenzoate-like LCMs with quantum chemical calculations. These results are useful for understanding the transformation and fate of LCMs in aquatic environments.