Synthesis of High χ–Low N Diblock Copolymers by Polymerization‐Induced Self‐Assembly

Polymerization‐induced self‐assembly (PISA) enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. Herein we exploit this versatile technique to produce so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid sta...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Angewandte Chemie International Edition 2020-06, Vol.59 (27), p.10848-10853
Hauptverfasser: Jennings, James, Cornel, Erik J., Derry, Matthew J., Beattie, Deborah L., Rymaruk, Matthew J., Deane, Oliver J., Ryan, Anthony J., Armes, Steven P.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 10853
container_issue 27
container_start_page 10848
container_title Angewandte Chemie International Edition
container_volume 59
creator Jennings, James
Cornel, Erik J.
Derry, Matthew J.
Beattie, Deborah L.
Rymaruk, Matthew J.
Deane, Oliver J.
Ryan, Anthony J.
Armes, Steven P.
description Polymerization‐induced self‐assembly (PISA) enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. Herein we exploit this versatile technique to produce so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid state to produce sub‐10 nm surface features. By varying the degree of polymerization of the stabilizer and core‐forming blocks, PISA provides rapid access to a wide range of diblock copolymers, and enables fundamental thermodynamic parameters to be determined. In addition, the pre‐organization of copolymer chains within sterically‐stabilized nanoparticles that occurs during PISA leads to enhanced phase separation relative to that achieved using solution‐cast molecularly‐dissolved copolymer chains. Polymerization‐induced self‐assembly enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. This versatile technique is exploited to prepare so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid state to produce sub‐10 nm domains.
doi_str_mv 10.1002/anie.202001436
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7317809</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2387656458</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4686-1930c6058cbe444ade0256721fabb4fe83e9d058474c4d6411eca0fa90b0f01c3</originalsourceid><addsrcrecordid>eNqFkb9uFDEQhy0EIiGhpUSWaNLs4X9rexuk0xGSk04BKVBRWF7vbM5hd32sbxNtqnS0SDwY75AnwacLR6Ch8ljz-dOMfwi9oGRCCWGvbedhwggjhAouH6F9mjOacaX441QLzjOlc7qHnsV4mXitiXyK9jhjUpE830efz8duvYToIw41PvUXS_zz293tj0W4xmf4rS-b4L7gWViFZmyhj7gc8Ydt7W_s2ofu7vb7vKsGBxU-h6ZO12mM0JbNeIie1LaJ8Pz-PECf3h1_nJ1mi_cn89l0kTkhtcxowYmTJNeuBCGErYCwXCpGa1uWogbNoahSWyjhRCUFpeAsqW1BSlIT6vgBerP1roayhcpBt-5tY1a9b20_mmC9-bvT-aW5CFdGcao0KZLg6F7Qh68DxLVpfXTQNLaDMETDuFYylyLXCX31D3oZhr5L6xkmNn9PCeeJmmwp14cYe6h3w1BiNrmZTW5ml1t68PLhCjv8d1AJKLbAtW9g_I_OTM_mx3_kvwA6uqiC</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2415211033</pqid></control><display><type>article</type><title>Synthesis of High χ–Low N Diblock Copolymers by Polymerization‐Induced Self‐Assembly</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Jennings, James ; Cornel, Erik J. ; Derry, Matthew J. ; Beattie, Deborah L. ; Rymaruk, Matthew J. ; Deane, Oliver J. ; Ryan, Anthony J. ; Armes, Steven P.</creator><creatorcontrib>Jennings, James ; Cornel, Erik J. ; Derry, Matthew J. ; Beattie, Deborah L. ; Rymaruk, Matthew J. ; Deane, Oliver J. ; Ryan, Anthony J. ; Armes, Steven P.</creatorcontrib><description>Polymerization‐induced self‐assembly (PISA) enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. Herein we exploit this versatile technique to produce so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid state to produce sub‐10 nm surface features. By varying the degree of polymerization of the stabilizer and core‐forming blocks, PISA provides rapid access to a wide range of diblock copolymers, and enables fundamental thermodynamic parameters to be determined. In addition, the pre‐organization of copolymer chains within sterically‐stabilized nanoparticles that occurs during PISA leads to enhanced phase separation relative to that achieved using solution‐cast molecularly‐dissolved copolymer chains. Polymerization‐induced self‐assembly enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. This versatile technique is exploited to prepare so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid state to produce sub‐10 nm domains.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202001436</identifier><identifier>PMID: 32267055</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Assembly ; Block copolymers ; Chemical synthesis ; Communication ; Communications ; Copolymers ; Degree of polymerization ; Morphology ; nanolithography ; nanoparticle processing ; Nanoparticles ; Phase separation ; Polymerization ; polymerization-induced self-assembly ; solid-state morphology</subject><ispartof>Angewandte Chemie International Edition, 2020-06, Vol.59 (27), p.10848-10853</ispartof><rights>2020 The Authors. Published by Wiley-VCH Verlag GmbH &amp; Co. KGaA.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4686-1930c6058cbe444ade0256721fabb4fe83e9d058474c4d6411eca0fa90b0f01c3</citedby><cites>FETCH-LOGICAL-c4686-1930c6058cbe444ade0256721fabb4fe83e9d058474c4d6411eca0fa90b0f01c3</cites><orcidid>0000-0002-8289-6351 ; 0000-0003-1213-4607</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.202001436$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.202001436$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,778,782,883,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32267055$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jennings, James</creatorcontrib><creatorcontrib>Cornel, Erik J.</creatorcontrib><creatorcontrib>Derry, Matthew J.</creatorcontrib><creatorcontrib>Beattie, Deborah L.</creatorcontrib><creatorcontrib>Rymaruk, Matthew J.</creatorcontrib><creatorcontrib>Deane, Oliver J.</creatorcontrib><creatorcontrib>Ryan, Anthony J.</creatorcontrib><creatorcontrib>Armes, Steven P.</creatorcontrib><title>Synthesis of High χ–Low N Diblock Copolymers by Polymerization‐Induced Self‐Assembly</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>Polymerization‐induced self‐assembly (PISA) enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. Herein we exploit this versatile technique to produce so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid state to produce sub‐10 nm surface features. By varying the degree of polymerization of the stabilizer and core‐forming blocks, PISA provides rapid access to a wide range of diblock copolymers, and enables fundamental thermodynamic parameters to be determined. In addition, the pre‐organization of copolymer chains within sterically‐stabilized nanoparticles that occurs during PISA leads to enhanced phase separation relative to that achieved using solution‐cast molecularly‐dissolved copolymer chains. Polymerization‐induced self‐assembly enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. This versatile technique is exploited to prepare so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid state to produce sub‐10 nm domains.</description><subject>Assembly</subject><subject>Block copolymers</subject><subject>Chemical synthesis</subject><subject>Communication</subject><subject>Communications</subject><subject>Copolymers</subject><subject>Degree of polymerization</subject><subject>Morphology</subject><subject>nanolithography</subject><subject>nanoparticle processing</subject><subject>Nanoparticles</subject><subject>Phase separation</subject><subject>Polymerization</subject><subject>polymerization-induced self-assembly</subject><subject>solid-state morphology</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNqFkb9uFDEQhy0EIiGhpUSWaNLs4X9rexuk0xGSk04BKVBRWF7vbM5hd32sbxNtqnS0SDwY75AnwacLR6Ch8ljz-dOMfwi9oGRCCWGvbedhwggjhAouH6F9mjOacaX441QLzjOlc7qHnsV4mXitiXyK9jhjUpE830efz8duvYToIw41PvUXS_zz293tj0W4xmf4rS-b4L7gWViFZmyhj7gc8Ydt7W_s2ofu7vb7vKsGBxU-h6ZO12mM0JbNeIie1LaJ8Pz-PECf3h1_nJ1mi_cn89l0kTkhtcxowYmTJNeuBCGErYCwXCpGa1uWogbNoahSWyjhRCUFpeAsqW1BSlIT6vgBerP1roayhcpBt-5tY1a9b20_mmC9-bvT-aW5CFdGcao0KZLg6F7Qh68DxLVpfXTQNLaDMETDuFYylyLXCX31D3oZhr5L6xkmNn9PCeeJmmwp14cYe6h3w1BiNrmZTW5ml1t68PLhCjv8d1AJKLbAtW9g_I_OTM_mx3_kvwA6uqiC</recordid><startdate>20200626</startdate><enddate>20200626</enddate><creator>Jennings, James</creator><creator>Cornel, Erik J.</creator><creator>Derry, Matthew J.</creator><creator>Beattie, Deborah L.</creator><creator>Rymaruk, Matthew J.</creator><creator>Deane, Oliver J.</creator><creator>Ryan, Anthony J.</creator><creator>Armes, Steven P.</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8289-6351</orcidid><orcidid>https://orcid.org/0000-0003-1213-4607</orcidid></search><sort><creationdate>20200626</creationdate><title>Synthesis of High χ–Low N Diblock Copolymers by Polymerization‐Induced Self‐Assembly</title><author>Jennings, James ; Cornel, Erik J. ; Derry, Matthew J. ; Beattie, Deborah L. ; Rymaruk, Matthew J. ; Deane, Oliver J. ; Ryan, Anthony J. ; Armes, Steven P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4686-1930c6058cbe444ade0256721fabb4fe83e9d058474c4d6411eca0fa90b0f01c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Assembly</topic><topic>Block copolymers</topic><topic>Chemical synthesis</topic><topic>Communication</topic><topic>Communications</topic><topic>Copolymers</topic><topic>Degree of polymerization</topic><topic>Morphology</topic><topic>nanolithography</topic><topic>nanoparticle processing</topic><topic>Nanoparticles</topic><topic>Phase separation</topic><topic>Polymerization</topic><topic>polymerization-induced self-assembly</topic><topic>solid-state morphology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jennings, James</creatorcontrib><creatorcontrib>Cornel, Erik J.</creatorcontrib><creatorcontrib>Derry, Matthew J.</creatorcontrib><creatorcontrib>Beattie, Deborah L.</creatorcontrib><creatorcontrib>Rymaruk, Matthew J.</creatorcontrib><creatorcontrib>Deane, Oliver J.</creatorcontrib><creatorcontrib>Ryan, Anthony J.</creatorcontrib><creatorcontrib>Armes, Steven P.</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jennings, James</au><au>Cornel, Erik J.</au><au>Derry, Matthew J.</au><au>Beattie, Deborah L.</au><au>Rymaruk, Matthew J.</au><au>Deane, Oliver J.</au><au>Ryan, Anthony J.</au><au>Armes, Steven P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of High χ–Low N Diblock Copolymers by Polymerization‐Induced Self‐Assembly</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2020-06-26</date><risdate>2020</risdate><volume>59</volume><issue>27</issue><spage>10848</spage><epage>10853</epage><pages>10848-10853</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>Polymerization‐induced self‐assembly (PISA) enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. Herein we exploit this versatile technique to produce so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid state to produce sub‐10 nm surface features. By varying the degree of polymerization of the stabilizer and core‐forming blocks, PISA provides rapid access to a wide range of diblock copolymers, and enables fundamental thermodynamic parameters to be determined. In addition, the pre‐organization of copolymer chains within sterically‐stabilized nanoparticles that occurs during PISA leads to enhanced phase separation relative to that achieved using solution‐cast molecularly‐dissolved copolymer chains. Polymerization‐induced self‐assembly enables the scalable synthesis of functional block copolymer nanoparticles with various morphologies. This versatile technique is exploited to prepare so‐called “high χ–low N” diblock copolymers that undergo nanoscale phase separation in the solid state to produce sub‐10 nm domains.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32267055</pmid><doi>10.1002/anie.202001436</doi><tpages>6</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0002-8289-6351</orcidid><orcidid>https://orcid.org/0000-0003-1213-4607</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1433-7851
ispartof Angewandte Chemie International Edition, 2020-06, Vol.59 (27), p.10848-10853
issn 1433-7851
1521-3773
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7317809
source Wiley Online Library Journals Frontfile Complete
subjects Assembly
Block copolymers
Chemical synthesis
Communication
Communications
Copolymers
Degree of polymerization
Morphology
nanolithography
nanoparticle processing
Nanoparticles
Phase separation
Polymerization
polymerization-induced self-assembly
solid-state morphology
title Synthesis of High χ–Low N Diblock Copolymers by Polymerization‐Induced Self‐Assembly
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T13%3A09%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20High%20%CF%87%E2%80%93Low%20N%20Diblock%20Copolymers%20by%20Polymerization%E2%80%90Induced%20Self%E2%80%90Assembly&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Jennings,%20James&rft.date=2020-06-26&rft.volume=59&rft.issue=27&rft.spage=10848&rft.epage=10853&rft.pages=10848-10853&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.202001436&rft_dat=%3Cproquest_pubme%3E2387656458%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2415211033&rft_id=info:pmid/32267055&rfr_iscdi=true