Synthesis of a Macromonomer Library from High-Temperature Acrylate Polymerization
The auto‐initiated high temperature acrylate polymerization represents a versatile route for the synthesis of macromonomer building blocks. Various macromonomers were synthesized via this route based on methyl, ethyl, n‐butyl, t‐butyl, 2‐ethylhexyl, isobornyl and 2‐[[(butylamino)carbonyl]oxy]ethyl a...
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Veröffentlicht in: | Macromolecular rapid communications. 2009-12, Vol.30 (23), p.2028-2035 |
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creator | Zorn, Anna-Marie Junkers, Thomas Barner-Kowollik, Christopher |
description | The auto‐initiated high temperature acrylate polymerization represents a versatile route for the synthesis of macromonomer building blocks. Various macromonomers were synthesized via this route based on methyl, ethyl, n‐butyl, t‐butyl, 2‐ethylhexyl, isobornyl and 2‐[[(butylamino)carbonyl]oxy]ethyl acrylate. The synthesis requires a temperature of 140 °C and is carried out in a 5 wt.‐% solution of hexyl acetate. The macromonomer library is fully characterized via electrospray ionization mass spectrometry (ESI‐MS). The amount of macromonomers containing the geminal double bond lies in between 82 and 95%, depending on the monomer type. The achievable molecular weight of the macromonomers is located between 800 and 2 000 g·mol−1 with a polydispersity of close to 1.6. In addition, it is demonstrated that radical initiators are useful add‐ons (to circumvent the inhibition time observed during initiator‐free synthesis) without interfering in the actual polymerization as no initiator‐fragment containing products are identified via high resolution mass spectrometry.
A library of acrylate based macromonomers is synthesized via a facile high temperature one pot – on step procedure. The purity of the obtained macromonomers is assessed via electrospray ionization mass spectrometry (ESI‐MS) and shown to be close to 90% in all cases. |
doi_str_mv | 10.1002/marc.200900536 |
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A library of acrylate based macromonomers is synthesized via a facile high temperature one pot – on step procedure. The purity of the obtained macromonomers is assessed via electrospray ionization mass spectrometry (ESI‐MS) and shown to be close to 90% in all cases.</description><identifier>ISSN: 1022-1336</identifier><identifier>EISSN: 1521-3927</identifier><identifier>DOI: 10.1002/marc.200900536</identifier><identifier>PMID: 21638491</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Acrylates ; Bonding ; Libraries ; macromonomers ; Mass spectrometry ; Monomers ; Polymerization ; radical polymerization ; Radicals ; self-initiated polymerization ; Synthesis ; β-scission</subject><ispartof>Macromolecular rapid communications., 2009-12, Vol.30 (23), p.2028-2035</ispartof><rights>Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4156-58f0c95db06e79ca75db46a1ec8b5545be7d75f3fcd84326fdca9e827ef333683</citedby><cites>FETCH-LOGICAL-c4156-58f0c95db06e79ca75db46a1ec8b5545be7d75f3fcd84326fdca9e827ef333683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmarc.200900536$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmarc.200900536$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21638491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zorn, Anna-Marie</creatorcontrib><creatorcontrib>Junkers, Thomas</creatorcontrib><creatorcontrib>Barner-Kowollik, Christopher</creatorcontrib><title>Synthesis of a Macromonomer Library from High-Temperature Acrylate Polymerization</title><title>Macromolecular rapid communications.</title><addtitle>Macromol. Rapid Commun</addtitle><description>The auto‐initiated high temperature acrylate polymerization represents a versatile route for the synthesis of macromonomer building blocks. Various macromonomers were synthesized via this route based on methyl, ethyl, n‐butyl, t‐butyl, 2‐ethylhexyl, isobornyl and 2‐[[(butylamino)carbonyl]oxy]ethyl acrylate. The synthesis requires a temperature of 140 °C and is carried out in a 5 wt.‐% solution of hexyl acetate. The macromonomer library is fully characterized via electrospray ionization mass spectrometry (ESI‐MS). The amount of macromonomers containing the geminal double bond lies in between 82 and 95%, depending on the monomer type. The achievable molecular weight of the macromonomers is located between 800 and 2 000 g·mol−1 with a polydispersity of close to 1.6. In addition, it is demonstrated that radical initiators are useful add‐ons (to circumvent the inhibition time observed during initiator‐free synthesis) without interfering in the actual polymerization as no initiator‐fragment containing products are identified via high resolution mass spectrometry.
A library of acrylate based macromonomers is synthesized via a facile high temperature one pot – on step procedure. The purity of the obtained macromonomers is assessed via electrospray ionization mass spectrometry (ESI‐MS) and shown to be close to 90% in all cases.</description><subject>Acrylates</subject><subject>Bonding</subject><subject>Libraries</subject><subject>macromonomers</subject><subject>Mass spectrometry</subject><subject>Monomers</subject><subject>Polymerization</subject><subject>radical polymerization</subject><subject>Radicals</subject><subject>self-initiated polymerization</subject><subject>Synthesis</subject><subject>β-scission</subject><issn>1022-1336</issn><issn>1521-3927</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v1DAQhq0KRD_gyhHlBpcsYzu2k-NqoR_qbqFfqsTFcpwxNSSbxc6qTX89Xm1ZcYLTjEbP-0rzEPKWwoQCsI-dCXbCACoAweUeOaCC0ZxXTL1IOzCWU87lPjmM8QcAlAWwV2SfUcnLoqIH5PJ6XA73GH3MepeZbGFs6Lt-2XcYsrmvgwlj5tIpO_Xf7_Mb7FYYzLAOmE1tGFszYPa1b8eE-ycz-H75mrx0po345nkekdvjzzez03z-5eRsNp3ntqBC5qJ0YCvR1CBRVdaotBbSULRlLUQhalSNEo4725QFZ9I11lRYMoWOp49KfkTeb3tXof-1xjjozkeLbWuW2K-jLhWwKonYkB_-SVKpaAEF5yyhky2aLMQY0OlV8MnxqCnojXC9Ea53wlPg3XP3uu6w2eF_DCeg2gIPvsXxP3V6Mb2a_V2eb7M-Dvi4y5rwU0vFldB3Fyf6_Pru4tvi01yf89_6rJzX</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Zorn, Anna-Marie</creator><creator>Junkers, Thomas</creator><creator>Barner-Kowollik, Christopher</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20091201</creationdate><title>Synthesis of a Macromonomer Library from High-Temperature Acrylate Polymerization</title><author>Zorn, Anna-Marie ; Junkers, Thomas ; Barner-Kowollik, Christopher</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4156-58f0c95db06e79ca75db46a1ec8b5545be7d75f3fcd84326fdca9e827ef333683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acrylates</topic><topic>Bonding</topic><topic>Libraries</topic><topic>macromonomers</topic><topic>Mass spectrometry</topic><topic>Monomers</topic><topic>Polymerization</topic><topic>radical polymerization</topic><topic>Radicals</topic><topic>self-initiated polymerization</topic><topic>Synthesis</topic><topic>β-scission</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zorn, Anna-Marie</creatorcontrib><creatorcontrib>Junkers, Thomas</creatorcontrib><creatorcontrib>Barner-Kowollik, Christopher</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Macromolecular rapid communications.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zorn, Anna-Marie</au><au>Junkers, Thomas</au><au>Barner-Kowollik, Christopher</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of a Macromonomer Library from High-Temperature Acrylate Polymerization</atitle><jtitle>Macromolecular rapid communications.</jtitle><addtitle>Macromol. Rapid Commun</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>30</volume><issue>23</issue><spage>2028</spage><epage>2035</epage><pages>2028-2035</pages><issn>1022-1336</issn><eissn>1521-3927</eissn><abstract>The auto‐initiated high temperature acrylate polymerization represents a versatile route for the synthesis of macromonomer building blocks. Various macromonomers were synthesized via this route based on methyl, ethyl, n‐butyl, t‐butyl, 2‐ethylhexyl, isobornyl and 2‐[[(butylamino)carbonyl]oxy]ethyl acrylate. The synthesis requires a temperature of 140 °C and is carried out in a 5 wt.‐% solution of hexyl acetate. The macromonomer library is fully characterized via electrospray ionization mass spectrometry (ESI‐MS). The amount of macromonomers containing the geminal double bond lies in between 82 and 95%, depending on the monomer type. The achievable molecular weight of the macromonomers is located between 800 and 2 000 g·mol−1 with a polydispersity of close to 1.6. In addition, it is demonstrated that radical initiators are useful add‐ons (to circumvent the inhibition time observed during initiator‐free synthesis) without interfering in the actual polymerization as no initiator‐fragment containing products are identified via high resolution mass spectrometry.
A library of acrylate based macromonomers is synthesized via a facile high temperature one pot – on step procedure. The purity of the obtained macromonomers is assessed via electrospray ionization mass spectrometry (ESI‐MS) and shown to be close to 90% in all cases.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>21638491</pmid><doi>10.1002/marc.200900536</doi><tpages>8</tpages></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete |
subjects | Acrylates Bonding Libraries macromonomers Mass spectrometry Monomers Polymerization radical polymerization Radicals self-initiated polymerization Synthesis β-scission |
title | Synthesis of a Macromonomer Library from High-Temperature Acrylate Polymerization |
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