Synthesis of ultrahigh molecular weight bottlebrush block copolymers of ω-end-norbornyl polystyrene and polymethacrylate macromonomers
Well-controlled polystyrene-polymethacrylate bottlebrush block copolymers (BBCPs) of ultrahigh molecular weight using ω-end-norbornyl polystyrene as the macromonomer for the first block were synthesized by combining living anionic polymerization (LAP) and ring-opening metathesis polymerization (ROMP...
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Veröffentlicht in: | Polymer (Guilford) 2019-08, Vol.177, p.241-249 |
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creator | Seo, Ho-Bin Yu, Yong-Guen Chae, Chang-Geun Kim, Myung-Jin Lee, Jae-Suk |
description | Well-controlled polystyrene-polymethacrylate bottlebrush block copolymers (BBCPs) of ultrahigh molecular weight using ω-end-norbornyl polystyrene as the macromonomer for the first block were synthesized by combining living anionic polymerization (LAP) and ring-opening metathesis polymerization (ROMP). The ω-end-norbornyl polystyrene (NB-PSt), poly(tert-butyl methacrylate) (NB-PtBMA), poly(methyl methacrylate) (NB-PMMA), and poly(benzyl methacrylate) (NB-PBzMA) macromonomers (MMs) were synthesized by the LAP. The ROMP of the MMs led to poly(NB-g-St) (molecular weight, Mn = 1515 kDa, and dispersity, Ð = 1.12), poly(NB-g-tBMA) (Mn = 1470 kDa, Ð = 1.49), poly(NB-g-MMA) (Mn = 1128 kDa, Ð = 1.42), and poly(NB-g-BzMA) (Mn = 941 kDa, Ð = 1.16) bottlebrush homopolymers at degree of polymerization (DP) of 500. Synthesis of the BBCP, P(NB-g-St)-b-P(NB-g-tBMA) was well-controlled with high molecular weight and a low dispersity (Mn = 3002 kDa, Ð = 1.17) with a total DP of 976. The self-assembly of the resulting BBCP films revealed periodic lamellar morphologies with characteristic photonic crystal properties.
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•Ultrahigh molecular weight BBCPs based on polystyrene and polymethylacrylates are synthesized for the first time.•The ROMP for NB-PSt as the first block led to facile and well-controlled ROMP of norbornyl-functionalized polymethacrylates.•The resulting BBCPs showed the characteristic photonic crystal properties except those of PSt and PBzMA. |
doi_str_mv | 10.1016/j.polymer.2019.06.009 |
format | Article |
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[Display omitted]
•Ultrahigh molecular weight BBCPs based on polystyrene and polymethylacrylates are synthesized for the first time.•The ROMP for NB-PSt as the first block led to facile and well-controlled ROMP of norbornyl-functionalized polymethacrylates.•The resulting BBCPs showed the characteristic photonic crystal properties except those of PSt and PBzMA.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2019.06.009</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Anionic polymerization ; Block copolymers ; Bottlebrush block copolymers ; Chemical synthesis ; Copolymers ; Degree of polymerization ; Dispersion ; Metathesis ; Molecular weight ; Morphology ; Photonic crystals ; Physical characteristics ; Polymerization ; Polymethyl methacrylate ; Polymethylmethacrylate ; Polystyrene ; Polystyrene resins ; Ring-opening metathesis polymerization ; Self-assembly</subject><ispartof>Polymer (Guilford), 2019-08, Vol.177, p.241-249</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright Elsevier BV Aug 26, 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c337t-effe977e9b66a79ab922f6607191c1d81834c45084e93e31b9af187292b3574c3</citedby><cites>FETCH-LOGICAL-c337t-effe977e9b66a79ab922f6607191c1d81834c45084e93e31b9af187292b3574c3</cites><orcidid>0000-0002-6611-2801</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0032386119305178$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids></links><search><creatorcontrib>Seo, Ho-Bin</creatorcontrib><creatorcontrib>Yu, Yong-Guen</creatorcontrib><creatorcontrib>Chae, Chang-Geun</creatorcontrib><creatorcontrib>Kim, Myung-Jin</creatorcontrib><creatorcontrib>Lee, Jae-Suk</creatorcontrib><title>Synthesis of ultrahigh molecular weight bottlebrush block copolymers of ω-end-norbornyl polystyrene and polymethacrylate macromonomers</title><title>Polymer (Guilford)</title><description>Well-controlled polystyrene-polymethacrylate bottlebrush block copolymers (BBCPs) of ultrahigh molecular weight using ω-end-norbornyl polystyrene as the macromonomer for the first block were synthesized by combining living anionic polymerization (LAP) and ring-opening metathesis polymerization (ROMP). The ω-end-norbornyl polystyrene (NB-PSt), poly(tert-butyl methacrylate) (NB-PtBMA), poly(methyl methacrylate) (NB-PMMA), and poly(benzyl methacrylate) (NB-PBzMA) macromonomers (MMs) were synthesized by the LAP. The ROMP of the MMs led to poly(NB-g-St) (molecular weight, Mn = 1515 kDa, and dispersity, Ð = 1.12), poly(NB-g-tBMA) (Mn = 1470 kDa, Ð = 1.49), poly(NB-g-MMA) (Mn = 1128 kDa, Ð = 1.42), and poly(NB-g-BzMA) (Mn = 941 kDa, Ð = 1.16) bottlebrush homopolymers at degree of polymerization (DP) of 500. Synthesis of the BBCP, P(NB-g-St)-b-P(NB-g-tBMA) was well-controlled with high molecular weight and a low dispersity (Mn = 3002 kDa, Ð = 1.17) with a total DP of 976. The self-assembly of the resulting BBCP films revealed periodic lamellar morphologies with characteristic photonic crystal properties.
[Display omitted]
•Ultrahigh molecular weight BBCPs based on polystyrene and polymethylacrylates are synthesized for the first time.•The ROMP for NB-PSt as the first block led to facile and well-controlled ROMP of norbornyl-functionalized polymethacrylates.•The resulting BBCPs showed the characteristic photonic crystal properties except those of PSt and PBzMA.</description><subject>Anionic polymerization</subject><subject>Block copolymers</subject><subject>Bottlebrush block copolymers</subject><subject>Chemical synthesis</subject><subject>Copolymers</subject><subject>Degree of polymerization</subject><subject>Dispersion</subject><subject>Metathesis</subject><subject>Molecular weight</subject><subject>Morphology</subject><subject>Photonic crystals</subject><subject>Physical characteristics</subject><subject>Polymerization</subject><subject>Polymethyl methacrylate</subject><subject>Polymethylmethacrylate</subject><subject>Polystyrene</subject><subject>Polystyrene resins</subject><subject>Ring-opening metathesis polymerization</subject><subject>Self-assembly</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkM1q3TAQhUVpIbdJHiEg6NqufmzLWpUS-hMIZJFkLWR5HPtWlm4lucVPUPJ0eaXKuXeflUbMOWdmPoSuKCkpoc3nfXnwdp0hlIxQWZKmJES-QzvaCl4wJul7tCOEs4K3DT1DH2PcE0JYzaod-ne_ujRCnCL2A15sCnqcnkY8ewtmsTrgv5D_CXc-JQtdWOKIO-vNL2z8aeyr9eW5ANcXzofOB7davDVjWgM4wNr1-ChOozZhtToBnnPlZ-_8FnGBPgzaRrg8vefo8fu3h-ufxe3dj5vrr7eF4VykAoYBpBAgu6bRQupOMjY0DRFUUkP7lra8MlVN2gokB047qYeMgUnW8VpUhp-jT8fcQ_C_F4hJ7f0SXB6pNlIVFUzUWVUfVXnDGAMM6hCmWYdVUaI25mqvTserjbkijcrMs-_L0Qf5hD9T7kYzgTPQTwFMUr2f3kj4D02Wki4</recordid><startdate>20190826</startdate><enddate>20190826</enddate><creator>Seo, Ho-Bin</creator><creator>Yu, Yong-Guen</creator><creator>Chae, Chang-Geun</creator><creator>Kim, Myung-Jin</creator><creator>Lee, Jae-Suk</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0002-6611-2801</orcidid></search><sort><creationdate>20190826</creationdate><title>Synthesis of ultrahigh molecular weight bottlebrush block copolymers of ω-end-norbornyl polystyrene and polymethacrylate macromonomers</title><author>Seo, Ho-Bin ; Yu, Yong-Guen ; Chae, Chang-Geun ; Kim, Myung-Jin ; Lee, Jae-Suk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-effe977e9b66a79ab922f6607191c1d81834c45084e93e31b9af187292b3574c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anionic polymerization</topic><topic>Block copolymers</topic><topic>Bottlebrush block copolymers</topic><topic>Chemical synthesis</topic><topic>Copolymers</topic><topic>Degree of polymerization</topic><topic>Dispersion</topic><topic>Metathesis</topic><topic>Molecular weight</topic><topic>Morphology</topic><topic>Photonic crystals</topic><topic>Physical characteristics</topic><topic>Polymerization</topic><topic>Polymethyl methacrylate</topic><topic>Polymethylmethacrylate</topic><topic>Polystyrene</topic><topic>Polystyrene resins</topic><topic>Ring-opening metathesis polymerization</topic><topic>Self-assembly</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seo, Ho-Bin</creatorcontrib><creatorcontrib>Yu, Yong-Guen</creatorcontrib><creatorcontrib>Chae, Chang-Geun</creatorcontrib><creatorcontrib>Kim, Myung-Jin</creatorcontrib><creatorcontrib>Lee, Jae-Suk</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seo, Ho-Bin</au><au>Yu, Yong-Guen</au><au>Chae, Chang-Geun</au><au>Kim, Myung-Jin</au><au>Lee, Jae-Suk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of ultrahigh molecular weight bottlebrush block copolymers of ω-end-norbornyl polystyrene and polymethacrylate macromonomers</atitle><jtitle>Polymer (Guilford)</jtitle><date>2019-08-26</date><risdate>2019</risdate><volume>177</volume><spage>241</spage><epage>249</epage><pages>241-249</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><abstract>Well-controlled polystyrene-polymethacrylate bottlebrush block copolymers (BBCPs) of ultrahigh molecular weight using ω-end-norbornyl polystyrene as the macromonomer for the first block were synthesized by combining living anionic polymerization (LAP) and ring-opening metathesis polymerization (ROMP). The ω-end-norbornyl polystyrene (NB-PSt), poly(tert-butyl methacrylate) (NB-PtBMA), poly(methyl methacrylate) (NB-PMMA), and poly(benzyl methacrylate) (NB-PBzMA) macromonomers (MMs) were synthesized by the LAP. The ROMP of the MMs led to poly(NB-g-St) (molecular weight, Mn = 1515 kDa, and dispersity, Ð = 1.12), poly(NB-g-tBMA) (Mn = 1470 kDa, Ð = 1.49), poly(NB-g-MMA) (Mn = 1128 kDa, Ð = 1.42), and poly(NB-g-BzMA) (Mn = 941 kDa, Ð = 1.16) bottlebrush homopolymers at degree of polymerization (DP) of 500. Synthesis of the BBCP, P(NB-g-St)-b-P(NB-g-tBMA) was well-controlled with high molecular weight and a low dispersity (Mn = 3002 kDa, Ð = 1.17) with a total DP of 976. The self-assembly of the resulting BBCP films revealed periodic lamellar morphologies with characteristic photonic crystal properties.
[Display omitted]
•Ultrahigh molecular weight BBCPs based on polystyrene and polymethylacrylates are synthesized for the first time.•The ROMP for NB-PSt as the first block led to facile and well-controlled ROMP of norbornyl-functionalized polymethacrylates.•The resulting BBCPs showed the characteristic photonic crystal properties except those of PSt and PBzMA.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2019.06.009</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6611-2801</orcidid></addata></record> |
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subjects | Anionic polymerization Block copolymers Bottlebrush block copolymers Chemical synthesis Copolymers Degree of polymerization Dispersion Metathesis Molecular weight Morphology Photonic crystals Physical characteristics Polymerization Polymethyl methacrylate Polymethylmethacrylate Polystyrene Polystyrene resins Ring-opening metathesis polymerization Self-assembly |
title | Synthesis of ultrahigh molecular weight bottlebrush block copolymers of ω-end-norbornyl polystyrene and polymethacrylate macromonomers |
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