Stereokontrolowana polimeryzacja chiralnych monomerów heterocyklicznych

A. Duda

Published : 2022-09-01

Vol. 49 No. 7-8 (2004)

Stereocontrolled polymerization of chiral heterocydic monomers

A. Duda

Abstract

A review with 80 references deals with stereoselective (race-mate-forming chirogenic) and stereoelective (asymmetric enantiomer-differentiating) ring-opening polymerizations of chiral oxiranes, thiiranes, lactones, dilactides, and N-carboxyanhydrides of alpha-aminoacids. These enantiocontrolled polymerizations are analyzed in terms of the chain-end control or site control mechanisms (CEM or SCM, respectively). Possibility of formation of highly ordered structures by the resulting izotactic and optically active macromolecules is also discussed.

Keywords

chiralne monomery heterocykliczne ; monomery heterocykliczne ; dilaktydy ; N-karboksybezwodniki alfa-aminokwasów ; laktony ; tiirany ; oksirany ; polimeryzacja z otwarciem pierścienia ; polimeryzacja stereoelektywna ; polimeryzacja stereoselektywna chiral heterocyclic monomers ; chiral polymers ; dilactides ; alpha-aminoacid N-carboxyanhydrides ; lactones ; thiiranes ; oxiranes ; ring opening polymerization ; stereoelective polymerization ; stereoselective polymerization

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Duda, A. (2022). Stereocontrolled polymerization of chiral heterocydic monomers. Polimery, 49(7-8), 469–478. Retrieved from https://polimery.ichp.vot.pl/index.php/p/article/view/1773

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