Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide

Detalhes bibliográficos
Autor(a) principal: Mendes, Paulo J.
Data de Publicação: 2016
Outros Autores: Ramalho, João P. Prates, Nogueira, Guilherme, Favrelle, Audrey, Bria, Marc, Valente, Andreia, Zinck, Philippe
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10174/19752
https://doi.org/10.1039/C6RE00061D
Resumo: Nucleobase-functionalized polymers are widely used in the fields of supramolecular chemistry and self-assembly, and their development for biomedical applications is also an area of interest. They are usually synthesized by tedious multistep procedures. In this study, we assess adenine as an organoinitiator/organocatalyst for the ring-opening polymerization of lactide. L-Lactide can be quantitatively polymerized in the presence of adenine. Reaction conditions involving short reaction times and relatively low temperatures enable the access to adenine end-capped polylactide in a simple one-step procedure, in bulk, without additional catalyst. DFT calculations show that the polymerization occurs via hydrogen bond catalysis. The mechanism involves (i) a hydrogen bond between the NH9 of adenine and the carbonyl moiety of lactide, leading to an electron deficient carbon atom, and (ii) a second hydrogen bond between the N3 of adenine and the NH2 of a second adenine molecule, followed by a nucleophilic attack of the latter activated amine on the former electron deficient carbon on the monomer. For longer reaction times and higher temperatures, macrocyclic species are formed, and a mechanism involving the imidazole ring of adenine is proposed based on literature studies. Depending on the reaction conditions, adenine can thus be considered as an organoinitiator or an organocatalyst for the ring-opening polymerization of lactide.
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spelling Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactidering-opening polymerizationorganocatalystAdeninepolylactideNucleobase-functionalized polymers are widely used in the fields of supramolecular chemistry and self-assembly, and their development for biomedical applications is also an area of interest. They are usually synthesized by tedious multistep procedures. In this study, we assess adenine as an organoinitiator/organocatalyst for the ring-opening polymerization of lactide. L-Lactide can be quantitatively polymerized in the presence of adenine. Reaction conditions involving short reaction times and relatively low temperatures enable the access to adenine end-capped polylactide in a simple one-step procedure, in bulk, without additional catalyst. DFT calculations show that the polymerization occurs via hydrogen bond catalysis. The mechanism involves (i) a hydrogen bond between the NH9 of adenine and the carbonyl moiety of lactide, leading to an electron deficient carbon atom, and (ii) a second hydrogen bond between the N3 of adenine and the NH2 of a second adenine molecule, followed by a nucleophilic attack of the latter activated amine on the former electron deficient carbon on the monomer. For longer reaction times and higher temperatures, macrocyclic species are formed, and a mechanism involving the imidazole ring of adenine is proposed based on literature studies. Depending on the reaction conditions, adenine can thus be considered as an organoinitiator or an organocatalyst for the ring-opening polymerization of lactide.Royal Society of Chemistry2017-01-12T17:09:02Z2017-01-122016-07-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/19752http://hdl.handle.net/10174/19752https://doi.org/10.1039/C6RE00061DengReact. Chem. Eng., 2016, 1, 508-520http://pubs.rsc.org/en/content/articlelanding/2016/re/c6re00061d#!divAbstractQUIpjgm@uevora.ptjpcar@uevora.ptguilherme.nogueira91@gmail.comaudrey.favrelle@ensc-lille.frMarc.Bria@univ-lille1.framvalente@fc.ul.ptphilippe.zinck@ensc-lille.fr307Mendes, Paulo J.Ramalho, João P. PratesNogueira, GuilhermeFavrelle, AudreyBria, MarcValente, AndreiaZinck, Philippeinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-01-03T19:09:12Zoai:dspace.uevora.pt:10174/19752Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:11:24.151199Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide
title Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide
spellingShingle Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide
Mendes, Paulo J.
ring-opening polymerization
organocatalyst
Adenine
polylactide
title_short Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide
title_full Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide
title_fullStr Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide
title_full_unstemmed Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide
title_sort Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide
author Mendes, Paulo J.
author_facet Mendes, Paulo J.
Ramalho, João P. Prates
Nogueira, Guilherme
Favrelle, Audrey
Bria, Marc
Valente, Andreia
Zinck, Philippe
author_role author
author2 Ramalho, João P. Prates
Nogueira, Guilherme
Favrelle, Audrey
Bria, Marc
Valente, Andreia
Zinck, Philippe
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mendes, Paulo J.
Ramalho, João P. Prates
Nogueira, Guilherme
Favrelle, Audrey
Bria, Marc
Valente, Andreia
Zinck, Philippe
dc.subject.por.fl_str_mv ring-opening polymerization
organocatalyst
Adenine
polylactide
topic ring-opening polymerization
organocatalyst
Adenine
polylactide
description Nucleobase-functionalized polymers are widely used in the fields of supramolecular chemistry and self-assembly, and their development for biomedical applications is also an area of interest. They are usually synthesized by tedious multistep procedures. In this study, we assess adenine as an organoinitiator/organocatalyst for the ring-opening polymerization of lactide. L-Lactide can be quantitatively polymerized in the presence of adenine. Reaction conditions involving short reaction times and relatively low temperatures enable the access to adenine end-capped polylactide in a simple one-step procedure, in bulk, without additional catalyst. DFT calculations show that the polymerization occurs via hydrogen bond catalysis. The mechanism involves (i) a hydrogen bond between the NH9 of adenine and the carbonyl moiety of lactide, leading to an electron deficient carbon atom, and (ii) a second hydrogen bond between the N3 of adenine and the NH2 of a second adenine molecule, followed by a nucleophilic attack of the latter activated amine on the former electron deficient carbon on the monomer. For longer reaction times and higher temperatures, macrocyclic species are formed, and a mechanism involving the imidazole ring of adenine is proposed based on literature studies. Depending on the reaction conditions, adenine can thus be considered as an organoinitiator or an organocatalyst for the ring-opening polymerization of lactide.
publishDate 2016
dc.date.none.fl_str_mv 2016-07-01T00:00:00Z
2017-01-12T17:09:02Z
2017-01-12
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10174/19752
http://hdl.handle.net/10174/19752
https://doi.org/10.1039/C6RE00061D
url http://hdl.handle.net/10174/19752
https://doi.org/10.1039/C6RE00061D
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv React. Chem. Eng., 2016, 1, 508-520
http://pubs.rsc.org/en/content/articlelanding/2016/re/c6re00061d#!divAbstract
QUI
pjgm@uevora.pt
jpcar@uevora.pt
guilherme.nogueira91@gmail.com
audrey.favrelle@ensc-lille.fr
Marc.Bria@univ-lille1.fr
amvalente@fc.ul.pt
philippe.zinck@ensc-lille.fr
307
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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