ABC and ABAB Block Copolymers by Electrochemically Controlled Ring-Opening Polymerization
An electrochemically controlled synthesis of multiblock copolymers by alternating the redox states of (salfan)Zr(OtBu)2 (salfan = 1,1′-di(2-tert-butyl-6-N-methylmethylenephenoxy)ferrocene) is reported. Aided by electrochemistry with a glassy carbon working electrode, an in situ potential switch...
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Veröffentlicht in: | Journal of the American Chemical Society 2021-12, Vol.143 (47), p.19802-19808 |
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container_end_page | 19808 |
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container_issue | 47 |
container_start_page | 19802 |
container_title | Journal of the American Chemical Society |
container_volume | 143 |
creator | Hern, Zachary C Quan, Stephanie M Dai, Ruxi Lai, Amy Wang, Yihang Liu, Chong Diaconescu, Paula L |
description | An electrochemically controlled synthesis of multiblock copolymers by alternating the redox states of (salfan)Zr(OtBu)2 (salfan = 1,1′-di(2-tert-butyl-6-N-methylmethylenephenoxy)ferrocene) is reported. Aided by electrochemistry with a glassy carbon working electrode, an in situ potential switch alters the catalyst’s oxidation state and its subsequent monomer (l-lactide, β-butyrolactone, or cyclohexene oxide) selectivity in one pot. Various multiblock copolymers were prepared, including an ABAB tetrablock copolymer, poly(cyclohexene oxide-b-lactide-b-cyclohexene oxide-b-lactide), and an ABC triblock copolymer, poly(hydroxybutyrate-b-cyclohexene oxide-b-lactide). The polymers produced using this technique are similar to those produced via a chemical redox reagent method, displaying moderately narrow dispersities (1.1–1.5) and molecular weights ranging from 7 to 26 kDa. |
doi_str_mv | 10.1021/jacs.1c08648 |
format | Article |
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Aided by electrochemistry with a glassy carbon working electrode, an in situ potential switch alters the catalyst’s oxidation state and its subsequent monomer (l-lactide, β-butyrolactone, or cyclohexene oxide) selectivity in one pot. Various multiblock copolymers were prepared, including an ABAB tetrablock copolymer, poly(cyclohexene oxide-b-lactide-b-cyclohexene oxide-b-lactide), and an ABC triblock copolymer, poly(hydroxybutyrate-b-cyclohexene oxide-b-lactide). 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Am. Chem. Soc</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>143</volume><issue>47</issue><spage>19802</spage><epage>19808</epage><pages>19802-19808</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>An electrochemically controlled synthesis of multiblock copolymers by alternating the redox states of (salfan)Zr(OtBu)2 (salfan = 1,1′-di(2-tert-butyl-6-N-methylmethylenephenoxy)ferrocene) is reported. Aided by electrochemistry with a glassy carbon working electrode, an in situ potential switch alters the catalyst’s oxidation state and its subsequent monomer (l-lactide, β-butyrolactone, or cyclohexene oxide) selectivity in one pot. Various multiblock copolymers were prepared, including an ABAB tetrablock copolymer, poly(cyclohexene oxide-b-lactide-b-cyclohexene oxide-b-lactide), and an ABC triblock copolymer, poly(hydroxybutyrate-b-cyclohexene oxide-b-lactide). The polymers produced using this technique are similar to those produced via a chemical redox reagent method, displaying moderately narrow dispersities (1.1–1.5) and molecular weights ranging from 7 to 26 kDa.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>34792339</pmid><doi>10.1021/jacs.1c08648</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-5546-3852</orcidid><orcidid>https://orcid.org/0000-0003-2732-4155</orcidid></addata></record> |
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title | ABC and ABAB Block Copolymers by Electrochemically Controlled Ring-Opening Polymerization |
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