UV-radiation curing of acrylate/epoxide systems was written by Decker, C.;Nguyen Thi Viet, T.;Decker, D.;Weber-Koehl, E.. And the article was included in Polymer in 2001.Synthetic Route of C30H56N2O4 This article mentions the following:
Interpenetrating polymer networks (IPNs) have been synthesized by light-induced crosslinking polymerization of a mixture of acrylate and epoxide monomers. The consumption of each monomer upon UV-irradiation in the presence of radical and cationic-type photoinitiators was monitored in situ by real-time IR spectroscopy. The acrylate monomer was shown to polymerize faster and more extensively than the epoxy monomer, which was further consumed upon storage of the sample in the dark, due to the living character of cationic polymerization Curing experiments carried out in the presence of air and under air diffusion-free conditions indicate that the radical polymerization of the acrylate monomer is hardly affected by the oxygen inhibition effect, while the cationic polymerization of the epoxy monomer is enhanced by the atm. humidity. The addition of a photosensitizer, like isopropylthioxanthone, was shown to speed up substantially the polymerization of the epoxide, with formation within seconds of two fully cured IPNs. In the experiment, the researchers used many compounds, for example, Bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate (cas: 41556-26-7Synthetic Route of C30H56N2O4).
Bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate (cas: 41556-26-7) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Piperidine derivatives bearing a masked aldehyde function in the ε-position are easily transformed into quinolizidine compounds through intramolecular reductive amination.Synthetic Route of C30H56N2O4
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem