“…[41] In the third report, the high price of O-perfluorocyclopentenyl substrate limits its application as a starting material for the coupling agent. [42] Taking into account the relatively low toxicity of eugenol, low cost caused by its natural abundance, high thermal stability, and chemical reactivity, this compound has recently been considered as a sustainable alternative for the preparation of high-performance epoxy thermosets, [43] self-healing polymers, [44] flame retardants, [45] coatings, [46] adhesives, [47] or electrode materials for batteries. [48] In this article, we would like to present a simple approach to the synthesis of a new family of biogenic SCAs based on an alkyl-aryl eugenol core, which is obtained by a two-step procedure that involves hydrosilylation of eugenol and its derivatives, and a series of nucleophilic substitution reactions with acyl and alkyl chlorides possessing different groups capable of interacting with polymer chains (i. e., alkenyl, epoxide, thiirane, thiocarbamoyl, thioether, and thioester moieties).…”