Synthesis of a Hyperbranched Polymer with Perfect Branching Based on Piperidine-4-one
A new class of a hyperbranched polymer with 100% degree of branching has been successfully prepared by using 1-(3-phenoxypropyl)piperidine-4-one as an AB2 monomer in the presence of methanesulfonic acid. This hyperbranched polymer is based upon a piperidine-4-one ring and is designed to react with a...
Gespeichert in:
Veröffentlicht in: | Macromolecules 2009-02, Vol.42 (4), p.994-1001 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1001 |
---|---|
container_issue | 4 |
container_start_page | 994 |
container_title | Macromolecules |
container_volume | 42 |
creator | Sinananwanich, Warapon Higashihara, Tomoya Ueda, Mitsuru |
description | A new class of a hyperbranched polymer with 100% degree of branching has been successfully prepared by using 1-(3-phenoxypropyl)piperidine-4-one as an AB2 monomer in the presence of methanesulfonic acid. This hyperbranched polymer is based upon a piperidine-4-one ring and is designed to react with aromatic nucleophiles to give an irreversibly formed diarylated compound. The electrophilicity of piperidine-4-one is enhanced by through-space electrostatic repulsion and an inductive effect. The kinetics of the model reaction between 1-ethylpiperidine-4-one and anisole was examined. The reaction followed second-order kinetics, indicating that the first reaction, that is, the formation of the intermediate from the reaction between 1-ethylpiperidine-4-one and anisole, is considerably slower than the second one, that is, the reaction of the generated intermediate with anisole. On the basis of this observation, a new monomer, which was expected to produce a 100% branched hyperbranched polymer, was designed and synthesized. The obtained polymer was characterized by 1H and 13C NMR spectroscopy, which affirmed the 100% degree of branching of the hyperbranched polymer. |
doi_str_mv | 10.1021/ma802516a |
format | Article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_ma802516a</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>d255128321</sourcerecordid><originalsourceid>FETCH-LOGICAL-a333t-1dcd09df77644c8d11622e41a8cb0d9ca55c45f7dc7c4154744230de1911001b3</originalsourceid><addsrcrecordid>eNptkDtPAzEQhC0EEiFQ8A_cUFAYdv3I3ZUkAoIUiUiQ-uT4QRwlvsg-hO7fcyEoNFRbzDejnSHkGuEOgeP9VpfAFY70CRmg4sBUKdQpGQBwySpeFefkIuc1AKKSYkAWb11sVy6HTBtPNZ12O5eWSUezcpbOm023dYl-hXZF5y55Z1o6_lFD_KBjnXuoiXQeelewITomWRPdJTnzepPd1e8dksXT4_tkymavzy-ThxnTQoiWoTUWKuuLYiSlKS3iiHMnUZdmCbYyWikjlS-sKYzs_y2k5AKswwqxb7AUQ3J7yDWpyTk5X-9S2OrU1Qj1fo_6uEfP3hzYnc5Gb_y-RchHA0cOCgT8cdrket18ptg3-CfvG3Pmar4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of a Hyperbranched Polymer with Perfect Branching Based on Piperidine-4-one</title><source>ACS Publications</source><creator>Sinananwanich, Warapon ; Higashihara, Tomoya ; Ueda, Mitsuru</creator><creatorcontrib>Sinananwanich, Warapon ; Higashihara, Tomoya ; Ueda, Mitsuru</creatorcontrib><description>A new class of a hyperbranched polymer with 100% degree of branching has been successfully prepared by using 1-(3-phenoxypropyl)piperidine-4-one as an AB2 monomer in the presence of methanesulfonic acid. This hyperbranched polymer is based upon a piperidine-4-one ring and is designed to react with aromatic nucleophiles to give an irreversibly formed diarylated compound. The electrophilicity of piperidine-4-one is enhanced by through-space electrostatic repulsion and an inductive effect. The kinetics of the model reaction between 1-ethylpiperidine-4-one and anisole was examined. The reaction followed second-order kinetics, indicating that the first reaction, that is, the formation of the intermediate from the reaction between 1-ethylpiperidine-4-one and anisole, is considerably slower than the second one, that is, the reaction of the generated intermediate with anisole. On the basis of this observation, a new monomer, which was expected to produce a 100% branched hyperbranched polymer, was designed and synthesized. The obtained polymer was characterized by 1H and 13C NMR spectroscopy, which affirmed the 100% degree of branching of the hyperbranched polymer.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma802516a</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Polycondensation ; Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><ispartof>Macromolecules, 2009-02, Vol.42 (4), p.994-1001</ispartof><rights>Copyright © 2009 American Chemical Society</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a333t-1dcd09df77644c8d11622e41a8cb0d9ca55c45f7dc7c4154744230de1911001b3</citedby><cites>FETCH-LOGICAL-a333t-1dcd09df77644c8d11622e41a8cb0d9ca55c45f7dc7c4154744230de1911001b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma802516a$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma802516a$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21205030$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Sinananwanich, Warapon</creatorcontrib><creatorcontrib>Higashihara, Tomoya</creatorcontrib><creatorcontrib>Ueda, Mitsuru</creatorcontrib><title>Synthesis of a Hyperbranched Polymer with Perfect Branching Based on Piperidine-4-one</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>A new class of a hyperbranched polymer with 100% degree of branching has been successfully prepared by using 1-(3-phenoxypropyl)piperidine-4-one as an AB2 monomer in the presence of methanesulfonic acid. This hyperbranched polymer is based upon a piperidine-4-one ring and is designed to react with aromatic nucleophiles to give an irreversibly formed diarylated compound. The electrophilicity of piperidine-4-one is enhanced by through-space electrostatic repulsion and an inductive effect. The kinetics of the model reaction between 1-ethylpiperidine-4-one and anisole was examined. The reaction followed second-order kinetics, indicating that the first reaction, that is, the formation of the intermediate from the reaction between 1-ethylpiperidine-4-one and anisole, is considerably slower than the second one, that is, the reaction of the generated intermediate with anisole. On the basis of this observation, a new monomer, which was expected to produce a 100% branched hyperbranched polymer, was designed and synthesized. The obtained polymer was characterized by 1H and 13C NMR spectroscopy, which affirmed the 100% degree of branching of the hyperbranched polymer.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polycondensation</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNptkDtPAzEQhC0EEiFQ8A_cUFAYdv3I3ZUkAoIUiUiQ-uT4QRwlvsg-hO7fcyEoNFRbzDejnSHkGuEOgeP9VpfAFY70CRmg4sBUKdQpGQBwySpeFefkIuc1AKKSYkAWb11sVy6HTBtPNZ12O5eWSUezcpbOm023dYl-hXZF5y55Z1o6_lFD_KBjnXuoiXQeelewITomWRPdJTnzepPd1e8dksXT4_tkymavzy-ThxnTQoiWoTUWKuuLYiSlKS3iiHMnUZdmCbYyWikjlS-sKYzs_y2k5AKswwqxb7AUQ3J7yDWpyTk5X-9S2OrU1Qj1fo_6uEfP3hzYnc5Gb_y-RchHA0cOCgT8cdrket18ptg3-CfvG3Pmar4</recordid><startdate>20090224</startdate><enddate>20090224</enddate><creator>Sinananwanich, Warapon</creator><creator>Higashihara, Tomoya</creator><creator>Ueda, Mitsuru</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20090224</creationdate><title>Synthesis of a Hyperbranched Polymer with Perfect Branching Based on Piperidine-4-one</title><author>Sinananwanich, Warapon ; Higashihara, Tomoya ; Ueda, Mitsuru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a333t-1dcd09df77644c8d11622e41a8cb0d9ca55c45f7dc7c4154744230de1911001b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polycondensation</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sinananwanich, Warapon</creatorcontrib><creatorcontrib>Higashihara, Tomoya</creatorcontrib><creatorcontrib>Ueda, Mitsuru</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sinananwanich, Warapon</au><au>Higashihara, Tomoya</au><au>Ueda, Mitsuru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of a Hyperbranched Polymer with Perfect Branching Based on Piperidine-4-one</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2009-02-24</date><risdate>2009</risdate><volume>42</volume><issue>4</issue><spage>994</spage><epage>1001</epage><pages>994-1001</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>A new class of a hyperbranched polymer with 100% degree of branching has been successfully prepared by using 1-(3-phenoxypropyl)piperidine-4-one as an AB2 monomer in the presence of methanesulfonic acid. This hyperbranched polymer is based upon a piperidine-4-one ring and is designed to react with aromatic nucleophiles to give an irreversibly formed diarylated compound. The electrophilicity of piperidine-4-one is enhanced by through-space electrostatic repulsion and an inductive effect. The kinetics of the model reaction between 1-ethylpiperidine-4-one and anisole was examined. The reaction followed second-order kinetics, indicating that the first reaction, that is, the formation of the intermediate from the reaction between 1-ethylpiperidine-4-one and anisole, is considerably slower than the second one, that is, the reaction of the generated intermediate with anisole. On the basis of this observation, a new monomer, which was expected to produce a 100% branched hyperbranched polymer, was designed and synthesized. The obtained polymer was characterized by 1H and 13C NMR spectroscopy, which affirmed the 100% degree of branching of the hyperbranched polymer.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma802516a</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0024-9297 |
ispartof | Macromolecules, 2009-02, Vol.42 (4), p.994-1001 |
issn | 0024-9297 1520-5835 |
language | eng |
recordid | cdi_crossref_primary_10_1021_ma802516a |
source | ACS Publications |
subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Polycondensation Preparation, kinetics, thermodynamics, mechanism and catalysts |
title | Synthesis of a Hyperbranched Polymer with Perfect Branching Based on Piperidine-4-one |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-15T17%3A59%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20a%20Hyperbranched%20Polymer%20with%20Perfect%20Branching%20Based%20on%20Piperidine-4-one&rft.jtitle=Macromolecules&rft.au=Sinananwanich,%20Warapon&rft.date=2009-02-24&rft.volume=42&rft.issue=4&rft.spage=994&rft.epage=1001&rft.pages=994-1001&rft.issn=0024-9297&rft.eissn=1520-5835&rft.coden=MAMOBX&rft_id=info:doi/10.1021/ma802516a&rft_dat=%3Cacs_cross%3Ed255128321%3C/acs_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |