Green Synthesis, Formulation and Test Field of L. (Lepidoptera: Lymantriidae) Sex Pheromone in East European Region.

The nun moth, L. (Linnaeus, 1758), is one of the most important defoliators of coniferous forests in Europe and Asia. In sexual communication, females produce three epoxides and an alkene: (-)-disparlure [(7,8)--7,8-epoxy-2-methyloctadecane], (+)-monachalure [(7,8)--7,8-epoxyoctadecane], (-)-monachalure [(7,8)--7,8-epoxyoctadecane], and their corresponding olefins.

Alkenyl pheromones: Raman spectroscopic analysis, DFT modeling, and machine learning for stereoisomerism evaluation.

Alkenyl pheromones are a class of insect sex pheromones that are characterized by the presence of one or more double bonds, which can be either in the E(trans) or Z(cis) configuration. This structural variation is essential in mating, as it influences reproductive behavior and provides a potential method for insect control. As a base for rapid and in-situ screening of synthetic pheromones or pheromone-based products, this study explores the potential of Raman spectroscopy to differentiate between the two geometrical isomers, E(trans) and Z(cis), of the alkenyl pheromones.