82971-57-1Relevant academic research and scientific papers
A ring to rule them all: A cyclic ketene acetal comonomer controls the nitroxide-mediated polymerization of methacrylates and confers tunable degradability
Delplace, Vianney,Guégain, Elise,Harrisson, Simon,Gigmes, Didier,Guillaneuf, Yohann,Nicolas, Julien
, p. 12847 - 12850 (2015)
2-Methylene-4-phenyl-1,3-dioxolane (MPDL) was successfully used as a controlling comonomer in NMP with oligo(ethylene glycol) methyl ether methacrylate (MeOEGMA) to prepare well-defined and degradable PEG-based P(MeOEGMA-co-MPDL) copolymers. The level of
Polyesters by a Radical Pathway: Rationalization of the Cyclic Ketene Acetal Efficiency
Gigmes, Didier,Gil, Noémie,Guillaneuf, Yohann,Lefay, Catherine,Plummer, Christopher M.,Siri, Didier,Tardy, Antoine
supporting information, p. 14517 - 14526 (2020/07/13)
Radical ring-opening polymerization (rROP) of cyclic ketene acetals (CKAs) combines the advantages of both ring-opening polymerization and radical polymerization thereby allowing the robust production of polyesters coupled with the mild polymerization conditions of a radical process. rROP was recently rejuvenated by the possibility to copolymerize CKAs with classic vinyl monomers leading to the insertion of cleavable functionality into a vinyl-based copolymer backbone and thus imparting (bio)degradability. Such materials are suitable for a large scope of applications, particularly within the biomedical field. The competition between the ring-opening and ring-retaining propagation routes is a major complication in the development of efficient CKA monomers, ultimately leading to the use of only four monomers that are known to completely ring-open under all experimental conditions. In this article we investigate the radical ring-opening polymerization of model CKA monomers and demonstrate by the combination of DFT calculations and kinetic modeling using PREDICI software that we are now able to predict in silico the ring-opening ability of CKA monomers.
Preparation of racemic and enantiomerically pure cyclic ketene acetals
Diaz-Ortiz,Diez-Barra,De La Hoz,Prieto
, p. 1935 - 1942 (2007/10/02)
Cyclic ketene acetals have been prepared from a-haloaldehyde dimethylacetals by transacetalization and subsequent elimination in PTC without solvent conditions. No racemization has been observed when an enantiomerically pure diol has been used. Stability and storage conditions have been studies.
