Mommer, Stefan; Keul, Helmut; Moeller, Martin published an article in 2014, the title of the article was Tailored Thiol-Functional Polyamides: Synthesis and Functionalization.Electric Literature of 6038-19-3 And the article contains the following content:
In this article, a synthetic concept for the preparation of polyamides with functional side groups is described. First, the synthesis of a bis(thiolactone) monomer is shown in a concise three-step route from itaconic acid and DL-homocysteine thiolactone. The reactivity of the resulting bis(thiolactone) toward hexyl amine is examined Next, the bis(thiolactone) is reacted as A,A-type monomer with different B,B-type comonomers (1,12-diaminododecane and 1,3-bis(aminopropyl)tetramethyldisiloxane). Ring opening of the thiolactones by the diamines leads to polyamides with pendant thiol groups. Using two diamines in different ratios, the properties of the resulting polyamides are tuned (thermal properties are determined) and different mol. weights are acquired. Subsequently, the thiol groups are reacted with Me acrylate via Michael addition to functionalize the polyamides. Functionalization of thiol-functional polyamides using poly(ethylene glycol) monomethyl ether (mPEG) acrylates (Mn = 480 and 1700 g mol-1) results in water-soluble amphiphilic poly-amides with mol. weights higher than 10 000 g mol-1. The experimental process involved the reaction of 3-Aminodihydrothiophen-2(3H)-one hydrochloride(cas: 6038-19-3).Electric Literature of 6038-19-3
The Article related to synthesis functionalization thiol functional polyamide, michael addition, polyamides, postpolymerization modification, thermal properties, thiols, Chemistry of Synthetic High Polymers: Ring-Opening and Other Polymerizations and other aspects.Electric Literature of 6038-19-3
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