Chemoselective Polymerizations from Mixtures of Epoxide, Lactone, Anhydride, and Carbon Dioxide
Author(s) -
Charles Romain,
Yunqing Zhu,
Paul Dingwall,
Shyeni Paul,
Henry S. Rzepa,
Antoine Buchard,
Charlotte K. Williams
Publication year - 2016
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.5b13070
Subject(s) - chemistry , epoxide , monomer , cyclohexene oxide , phthalic anhydride , copolymer , polymerization , polymer chemistry , propylene oxide , catalysis , polymer , ring opening polymerization , reactivity (psychology) , selectivity , lactone , organic chemistry , ethylene oxide , medicine , alternative medicine , pathology
Controlling polymer composition starting from mixtures of monomers is an important, but rarely achieved, target. Here a single switchable catalyst for both ring-opening polymerization (ROP) of lactones and ring-opening copolymerization (ROCOP) of epoxides, anhydrides, and CO2 is investigated, using both experimental and theoretical methods. Different combinations of four model monomers-ε-caprolactone, cyclohexene oxide, phthalic anhydride, and carbon dioxide-are investigated using a single dizinc catalyst. The catalyst switches between the distinct polymerization cycles and shows high monomer selectivity, resulting in block sequence control and predictable compositions (esters and carbonates) in the polymer chain. The understanding gained of the orthogonal reactivity of monomers, specifically controlled by the nature of the metal-chain end group, opens the way to engineer polymer block sequences.
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