Organocatalyzed chemoselective ring-opening polymerizations
نویسندگان
چکیده
منابع مشابه
Photoswitchable NHC-promoted ring-opening polymerizations.
The UV-induced photocyclization of a dithienylethene-annulated N-heterocyclic carbene precatalyst enabled photoswitchable ring-opening polymerizations of ε-caprolactone and δ-valerolactone. The polymerizations proceeded efficiently in ambient light, however UV irradiation attenuated the reaction rate (k(amb)/k(UV) = 59). Subsequent visible light exposure reversed the photocyclization and restor...
متن کاملPreparation of enantiomerically pure open calcocene and strontocene complexes and their application in ring opening polymerizations of rac-lactide.
The synthesis of C2 symmetric enantiomerically pure open Ca and Sr metallocenes, [(η(5)-pdl*)2Ca(thf)] (1) and [(η(5)-pdl*)2Sr(thf)2] (2) (pdl* = dimethylnopadienyl) is described and these complexes were fully characterized. The solid state structures confirm that the pdl* ligands coordinate exclusively with the less sterically demanding site to the Ca and Sr atoms. These complexes are active c...
متن کاملOrganocatalytic ring-opening polymerization.
Modern synthetic methods have revolutionized polymer chemistry through the development of new and powerful strategies for the controlled synthesis of complex polymer architectures.1-5 Many of these developments were spawned by new classes of transition metal catalysts for the synthesis of new polyolefin microstructures,5 the design of highly efficient families of “living” polymerization strateg...
متن کاملEnantioselective Ring-Opening
Ever since Nugent first reported a practical, catalytic method for the enantioselective opening of meso-epoxides with trimethylsilyl azide (TMSN3), [1] such desymmetrization reactions of epoxides and aziridines using a variety of nucleophiles have been the subject of extensive research. The less developed ring-opening reactions, those of meso-aziridines by carbon and nitrogen nucleophiles, give...
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ژورنال
عنوان ژورنال: Scientific Reports
سال: 2018
ISSN: 2045-2322
DOI: 10.1038/s41598-018-22171-6