Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization

A series of polyethylenes containing 21-carbon alkyl branches have been synthesized by acyclic diene metathesis (ADMET) polymerization. These 21-carbon alkyl branches are precisely placed on every 15th, 19th, 21st, 23rd, and 39th carbon along the polymer backbone. Precision of primary structures of...

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Autores:
Rojas Jiménez, Giovanni
Wagener, Kenneth Boone
Li, Hong
Tipo de recurso:
Article of investigation
Fecha de publicación:
2015
Institución:
Universidad ICESI
Repositorio:
Repositorio ICESI
Idioma:
eng
OAI Identifier:
oai:repository.icesi.edu.co:10906/81448
Acceso en línea:
https://www.scopus.com/record/display.uri?eid=2-s2.0-84947219803&origin=inward&txGid=BDF84BF6519D351F136F42A23D9C086E.wsnAw8kcdt7IPYLO0V48gA%3a2
http://hdl.handle.net/10906/81448
Palabra clave:
Polietileno
Metátesis
Carbono
Química orgánica
Métodos de investigación en bioquímica
Biochemistry research
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
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oai_identifier_str oai:repository.icesi.edu.co:10906/81448
network_acronym_str ICESI2
network_name_str Repositorio ICESI
repository_id_str
dc.title.spa.fl_str_mv Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization
title Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization
spellingShingle Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization
Polietileno
Metátesis
Carbono
Química orgánica
Métodos de investigación en bioquímica
Biochemistry research
title_short Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization
title_full Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization
title_fullStr Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization
title_full_unstemmed Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization
title_sort Precision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerization
dc.creator.fl_str_mv Rojas Jiménez, Giovanni
Wagener, Kenneth Boone
Li, Hong
dc.contributor.author.spa.fl_str_mv Rojas Jiménez, Giovanni
Wagener, Kenneth Boone
Li, Hong
dc.subject.spa.fl_str_mv Polietileno
Metátesis
Carbono
Química orgánica
Métodos de investigación en bioquímica
Biochemistry research
topic Polietileno
Metátesis
Carbono
Química orgánica
Métodos de investigación en bioquímica
Biochemistry research
description A series of polyethylenes containing 21-carbon alkyl branches have been synthesized by acyclic diene metathesis (ADMET) polymerization. These 21-carbon alkyl branches are precisely placed on every 15th, 19th, 21st, 23rd, and 39th carbon along the polymer backbone. Precision of primary structures of all polymers is verified by 1H and 13C NMR spectroscopy. All polymers present well-defined melting profiles, even at a high branch incorporation (13.3% mol). The melting temperature increases as the branch frequency decreases, similar to what we observed for short-chain branched polyethylenes. These observations together with a good linear relationship derived from Flory's theory suggest the exclusion of 21-carbon side chains from polyethylene crystal units.
publishDate 2015
dc.date.issued.none.fl_str_mv 2015-10-21
dc.date.accessioned.none.fl_str_mv 2017-05-18T02:37:56Z
dc.date.available.none.fl_str_mv 2017-05-18T02:37:56Z
dc.type.spa.fl_str_mv info:eu-repo/semantics/article
dc.type.coar.none.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.local.spa.fl_str_mv Artículo
dc.type.version.spa.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.none.fl_str_mv 10.1021/acsmacrolett.5b00641
dc.identifier.issn.none.fl_str_mv 2161-1653
dc.identifier.other.none.fl_str_mv https://www.scopus.com/record/display.uri?eid=2-s2.0-84947219803&origin=inward&txGid=BDF84BF6519D351F136F42A23D9C086E.wsnAw8kcdt7IPYLO0V48gA%3a2
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10906/81448
dc.identifier.instname.none.fl_str_mv instname: Universidad Icesi
dc.identifier.reponame.none.fl_str_mv reponame: Biblioteca Digital
dc.identifier.repourl.none.fl_str_mv repourl: https://repository.icesi.edu.co/
identifier_str_mv 10.1021/acsmacrolett.5b00641
2161-1653
instname: Universidad Icesi
reponame: Biblioteca Digital
repourl: https://repository.icesi.edu.co/
url https://www.scopus.com/record/display.uri?eid=2-s2.0-84947219803&origin=inward&txGid=BDF84BF6519D351F136F42A23D9C086E.wsnAw8kcdt7IPYLO0V48gA%3a2
http://hdl.handle.net/10906/81448
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv ACS Macro Letters, Vol. 4, No. 11 -2015
dc.rights.uri.none.fl_str_mv https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.accessrights.spa.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.license.none.fl_str_mv Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
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rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/4.0/
Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.extent.spa.fl_str_mv 3 páginas
dc.format.medium.spa.fl_str_mv Digital
dc.coverage.spatial.spa.fl_str_mv Washington de Lat: 45 33 00 N degrees minutes Lat: 45.5500 decimal degrees Long: 122 05 00 W degrees minutes Long: -122.0833 decimal degrees
dc.publisher.spa.fl_str_mv American Chemical Society -
dc.publisher.faculty.spa.fl_str_mv Facultad de Ciencias Naturales
dc.publisher.program.spa.fl_str_mv Química con énfasis en Bioquimica
dc.publisher.department.spa.fl_str_mv Departamento de Ciencias Químicas
dc.publisher.place.spa.fl_str_mv Washington
institution Universidad ICESI
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spelling Rojas Jiménez, GiovanniWagener, Kenneth BooneLi, Honggrojas@icesi.edu.coWashington de Lat: 45 33 00 N degrees minutes Lat: 45.5500 decimal degrees Long: 122 05 00 W degrees minutes Long: -122.0833 decimal degrees2017-05-18T02:37:56Z2017-05-18T02:37:56Z2015-10-2110.1021/acsmacrolett.5b006412161-1653https://www.scopus.com/record/display.uri?eid=2-s2.0-84947219803&origin=inward&txGid=BDF84BF6519D351F136F42A23D9C086E.wsnAw8kcdt7IPYLO0V48gA%3a2http://hdl.handle.net/10906/81448instname: Universidad Icesireponame: Biblioteca Digitalrepourl: https://repository.icesi.edu.co/A series of polyethylenes containing 21-carbon alkyl branches have been synthesized by acyclic diene metathesis (ADMET) polymerization. These 21-carbon alkyl branches are precisely placed on every 15th, 19th, 21st, 23rd, and 39th carbon along the polymer backbone. Precision of primary structures of all polymers is verified by 1H and 13C NMR spectroscopy. All polymers present well-defined melting profiles, even at a high branch incorporation (13.3% mol). The melting temperature increases as the branch frequency decreases, similar to what we observed for short-chain branched polyethylenes. These observations together with a good linear relationship derived from Flory's theory suggest the exclusion of 21-carbon side chains from polyethylene crystal units.3 páginasDigitalengAmerican Chemical Society -Facultad de Ciencias NaturalesQuímica con énfasis en BioquimicaDepartamento de Ciencias QuímicasWashingtonACS Macro Letters, Vol. 4, No. 11 -2015EL AUTOR, expresa que la obra objeto de la presente autorización es original y la elaboró sin quebrantar ni suplantar los derechos de autor de terceros, y de tal forma, la obra es de su exclusiva autoría y tiene la titularidad sobre éste. PARÁGRAFO: en caso de queja o acción por parte de un tercero referente a los derechos de autor sobre el artículo, folleto o libro en cuestión, EL AUTOR, asumirá la responsabilidad total, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos, la Universidad Icesi actúa como un tercero de buena fe. Esta autorización, permite a la Universidad Icesi, de forma indefinida, para que en los términos establecidos en la Ley 23 de 1982, la Ley 44 de 1993, leyes y jurisprudencia vigente al respecto, haga publicación de este con fines educativos Todo persona que consulte ya sea la biblioteca o en medio electrónico podrá copiar apartes del texto citando siempre la fuentes, es decir el título del trabajo y el autor.https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessAtribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)http://purl.org/coar/access_right/c_abf2PolietilenoMetátesisCarbonoQuímica orgánicaMétodos de investigación en bioquímicaBiochemistry researchPrecision Long-Chain Branched Polyethylene via Acyclic Diene Metathesis Polymerizationinfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_2df8fbb1Artículoinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85Comunidad Universidad Icesi - Investigadores41112251228ORIGINALdocumento.htmldocumento.htmltext/html323http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/81448/6/documento.html53353cb78a8be3f2d8297e3fecec841eMD56CC-LICENSElicense_urllicense_urltext/plain49http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/81448/2/license_url4afdbb8c545fd630ea7db775da747b2fMD52license_textlicense_textapplication/octet-stream0http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/81448/3/license_textd41d8cd98f00b204e9800998ecf8427eMD53license_rdflicense_rdfapplication/octet-stream0http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/81448/4/license_rdfd41d8cd98f00b204e9800998ecf8427eMD54LICENSElicense.txtlicense.txttext/plain1783http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/81448/5/license.txta9bf6c9d51cc761c4b473f39f5bcb2eaMD5510906/81448oai:repository.icesi.edu.co:10906/814482018-10-17 17:53:46.422Biblioteca Digital - Universidad icesicdcriollo@icesi.edu.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