《Chiral stimuli-responsive metallo-supramolecular assembly induced by CuII/CuI redox change》 was published in Chemical Communications (Cambridge, United Kingdom) in 2020. These research results belong to Marinova, Maya; Bonnefont, Antoine; Achard, Thierry; Maisse-Francois, Aline; Bellemin-Laponnaz, Stephane. Synthetic Route of C8H14O4 The article mentions the following:
Authors investigated the selective formation of homoleptic and heteroleptic metal complexes controlled by the chiral mol. instruction of the ligand and the coordination geometry of the metal. The results showed that chiral self-recognition or self-discrimination may be induced by the CuI/CuII redox transition using cyclic voltammetry. The further use of chiral ditopic ligands led to metallo-supramol. copolymers with stimuli-responsive controlled arrangement. In the experiment, the researchers used many compounds, for example, Diethyl 2-methylmalonate(cas: 609-08-5Synthetic Route of C8H14O4)
Diethyl 2-methylmalonate(cas: 609-08-5) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Synthetic Route of C8H14O4
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics