On September 27, 2022, Duss, Michael; Soto, Miguel A.; Patrick, Brian O.; MacLachlan, Mark J. published an article.Safety of 1,3-Diphenylurea The title of the article was A Supramolecular Strategy for the Synthesis of Cyclic Oligomers and Polymers by Ring Expansion. And the article contained the following:
Ring-opening metathesis polymerization (ROMP) of strained macrocycles is a key method to prepare diverse polymers. However, lack of ring strain in most macrocycles is an impediment to polymerization In this paper, the polymerization/oligomerization of unstrained macrocycles was achieved using a supramol. approach, leading selectively to cyclic products. Di-Ph thiourea and other guest mols. were used as additives to the ROMP reaction of unstrained macrocycles. An intermediate host-guest complex leads to the stabilization of the open form of the macrocycle after treatment with Grubbs catalysts, thereby favoring polymerization by inhibiting the ring-closing reaction back to the monomer. This proof-of-concept enables ring-expansion polymerization of unstrained macrocycles leading to cyclic polymers with mol. weights up to 6700 Da. The experimental process involved the reaction of 1,3-Diphenylurea(cas: 102-07-8).Safety of 1,3-Diphenylurea
The Article related to supramol cyclic oligomer polymer ring expansion, cyclic polymers, host-guest chemistry, macrocycle, olefin metathesis, supramolecular chemistry, Chemistry of Synthetic High Polymers: Other and other aspects.Safety of 1,3-Diphenylurea
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Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics