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Synthesis of Cis,syndiotactic A-alt-B Copolymers from Two Enantiomerically Pure Trans-2,3-Disubstituted-5,6-Norbornenes

[Image: see text] Cis,syndiotacticA-alt-B copolymers, where A and B are two enantiomerically pure trans-2,3-disubstituted-5,6-norbornenes with “opposite” chiralities, can be prepared with stereogenic-at-metal initiators of the type M(NR)(CHR′)(OR”)(pyrrolide). Formation of a high percentage of alter...

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Autores principales: Jang, Eun Sil, John, Jeremy M., Schrock, Richard R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043441/
https://www.ncbi.nlm.nih.gov/pubmed/27725961
http://dx.doi.org/10.1021/acscentsci.6b00200
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author Jang, Eun Sil
John, Jeremy M.
Schrock, Richard R.
author_facet Jang, Eun Sil
John, Jeremy M.
Schrock, Richard R.
author_sort Jang, Eun Sil
collection PubMed
description [Image: see text] Cis,syndiotacticA-alt-B copolymers, where A and B are two enantiomerically pure trans-2,3-disubstituted-5,6-norbornenes with “opposite” chiralities, can be prepared with stereogenic-at-metal initiators of the type M(NR)(CHR′)(OR”)(pyrrolide). Formation of a high percentage of alternating AB copolymer linkages relies on an inversion of chirality at the metal with each propagating step and a relatively fast formation of an AB sequence as a consequence of a preferred diastereomeric relationship between the chirality at the metal and the chirality of the monomer. This approach to formation of an alternating AB copolymer contrasts dramatically with the principle of forming AB copolymers from achiral monomers and catalysts.
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spelling pubmed-50434412016-10-10 Synthesis of Cis,syndiotactic A-alt-B Copolymers from Two Enantiomerically Pure Trans-2,3-Disubstituted-5,6-Norbornenes Jang, Eun Sil John, Jeremy M. Schrock, Richard R. ACS Cent Sci [Image: see text] Cis,syndiotacticA-alt-B copolymers, where A and B are two enantiomerically pure trans-2,3-disubstituted-5,6-norbornenes with “opposite” chiralities, can be prepared with stereogenic-at-metal initiators of the type M(NR)(CHR′)(OR”)(pyrrolide). Formation of a high percentage of alternating AB copolymer linkages relies on an inversion of chirality at the metal with each propagating step and a relatively fast formation of an AB sequence as a consequence of a preferred diastereomeric relationship between the chirality at the metal and the chirality of the monomer. This approach to formation of an alternating AB copolymer contrasts dramatically with the principle of forming AB copolymers from achiral monomers and catalysts. American Chemical Society 2016-09-06 2016-09-28 /pmc/articles/PMC5043441/ /pubmed/27725961 http://dx.doi.org/10.1021/acscentsci.6b00200 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Jang, Eun Sil
John, Jeremy M.
Schrock, Richard R.
Synthesis of Cis,syndiotactic A-alt-B Copolymers from Two Enantiomerically Pure Trans-2,3-Disubstituted-5,6-Norbornenes
title Synthesis of Cis,syndiotactic A-alt-B Copolymers from Two Enantiomerically Pure Trans-2,3-Disubstituted-5,6-Norbornenes
title_full Synthesis of Cis,syndiotactic A-alt-B Copolymers from Two Enantiomerically Pure Trans-2,3-Disubstituted-5,6-Norbornenes
title_fullStr Synthesis of Cis,syndiotactic A-alt-B Copolymers from Two Enantiomerically Pure Trans-2,3-Disubstituted-5,6-Norbornenes
title_full_unstemmed Synthesis of Cis,syndiotactic A-alt-B Copolymers from Two Enantiomerically Pure Trans-2,3-Disubstituted-5,6-Norbornenes
title_short Synthesis of Cis,syndiotactic A-alt-B Copolymers from Two Enantiomerically Pure Trans-2,3-Disubstituted-5,6-Norbornenes
title_sort synthesis of cis,syndiotactic a-alt-b copolymers from two enantiomerically pure trans-2,3-disubstituted-5,6-norbornenes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043441/
https://www.ncbi.nlm.nih.gov/pubmed/27725961
http://dx.doi.org/10.1021/acscentsci.6b00200
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