Characterization of commercial aliphatic hyperbranched polyesters

Commercially available Boltorn H x ( x=20, 30) hyperbranched (HB) polyesters of different theoretical core/monomer ratio (1/12 for H20 and 1/28 for H30) were characterized with respect to molar mass, composition, and structure. The results were compared to those obtained for the Boltorn H40 with a c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Polymer (Guilford) 2006-01, Vol.47 (1), p.166-175
Hauptverfasser: Žagar, Ema, Žigon, Majda, Podzimek, Stepan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 175
container_issue 1
container_start_page 166
container_title Polymer (Guilford)
container_volume 47
creator Žagar, Ema
Žigon, Majda
Podzimek, Stepan
description Commercially available Boltorn H x ( x=20, 30) hyperbranched (HB) polyesters of different theoretical core/monomer ratio (1/12 for H20 and 1/28 for H30) were characterized with respect to molar mass, composition, and structure. The results were compared to those obtained for the Boltorn H40 with a core/monomer ratio of 1/60 [Žagar E, Žigon M. Macromolecules 2002;35:9913 [11]]. The main side reaction in the pseudo one-pot synthesis of Boltorn polymers is a self-condensation of bis-MPA leading to the formation of HB structures without a core molecule. These are actually branches containing an unreacted carboxyl group. The fraction of HB structures without a core molecule increases with decreasing core/monomer ratio due to the decreasing fraction of HB structures with a core molecule. Since HB structures without a core molecule are of lower molar masses than HB structures with a core molecule, they particularly decrease the number average molar masses of the samples compared to the theoretically calculated ones. The polydispersity of Boltorn H x increases with decreasing core/monomer ratio. Some of the hydroxyl groups were found to react intramoleculary forming ether bonds. Boltorn H x polyesters have low degrees of branching due to the limited carboxyl group conversions, low DP n values, the presence of the core unit, and lower reactivity of hydroxyl groups in linear repeat units compared to those in terminal ones. The degree of branching according to Frey increases with decreasing core/monomer ratio.
doi_str_mv 10.1016/j.polymer.2005.10.142
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_28855318</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0032386105016290</els_id><sourcerecordid>28694373</sourcerecordid><originalsourceid>FETCH-LOGICAL-c467t-88cbbc31ffa5df2d138e0803b3c5e815b995d252c488487bd32445800c84fdf13</originalsourceid><addsrcrecordid>eNqNkEtLxDAUhYMoOI7-BKEb3bXm2aYrGQZfMOBG1yG9TWiGvkw6wvjrTZ0Bl7q6cO93zrkchK4Jzggm-d02G4d23xmfUYxFNq85PUELIguWUlqSU7TAmNGUyZyco4sQthhjKihfoNW60V7DZLz70pMb-mSwCQxddAOn20S3bmziAZJmPxpfed1DY-pkTjQhysIlOrO6DebqOJfo_fHhbf2cbl6fXtarTQo8L6ZUSqgqYMRaLWpLa8KkwRKzioEwkoiqLEUdfwIuJZdFVTPKuZAYg-S2toQt0e3Bd_TDxy5mq84FMG2rezPsgqJSCsGI_AeYl5wVLILiAIIfQvDGqtG7Tvu9IljNzaqtOjar5mZ_1pxG3c0xQAfQrZ07ceFXXEhCCoojd3_gTKzl00WXAM70YGrnDUyqHtwfSd-9Q5Iv</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>28694373</pqid></control><display><type>article</type><title>Characterization of commercial aliphatic hyperbranched polyesters</title><source>Elsevier ScienceDirect Journals</source><creator>Žagar, Ema ; Žigon, Majda ; Podzimek, Stepan</creator><creatorcontrib>Žagar, Ema ; Žigon, Majda ; Podzimek, Stepan</creatorcontrib><description>Commercially available Boltorn H x ( x=20, 30) hyperbranched (HB) polyesters of different theoretical core/monomer ratio (1/12 for H20 and 1/28 for H30) were characterized with respect to molar mass, composition, and structure. The results were compared to those obtained for the Boltorn H40 with a core/monomer ratio of 1/60 [Žagar E, Žigon M. Macromolecules 2002;35:9913 [11]]. The main side reaction in the pseudo one-pot synthesis of Boltorn polymers is a self-condensation of bis-MPA leading to the formation of HB structures without a core molecule. These are actually branches containing an unreacted carboxyl group. The fraction of HB structures without a core molecule increases with decreasing core/monomer ratio due to the decreasing fraction of HB structures with a core molecule. Since HB structures without a core molecule are of lower molar masses than HB structures with a core molecule, they particularly decrease the number average molar masses of the samples compared to the theoretically calculated ones. The polydispersity of Boltorn H x increases with decreasing core/monomer ratio. Some of the hydroxyl groups were found to react intramoleculary forming ether bonds. Boltorn H x polyesters have low degrees of branching due to the limited carboxyl group conversions, low DP n values, the presence of the core unit, and lower reactivity of hydroxyl groups in linear repeat units compared to those in terminal ones. The degree of branching according to Frey increases with decreasing core/monomer ratio.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2005.10.142</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Dendritic ; Exact sciences and technology ; Hyperbranched ; Organic polymers ; Physicochemistry of polymers ; Polyesters ; Properties and characterization ; Structure, morphology and analysis</subject><ispartof>Polymer (Guilford), 2006-01, Vol.47 (1), p.166-175</ispartof><rights>2006 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-88cbbc31ffa5df2d138e0803b3c5e815b995d252c488487bd32445800c84fdf13</citedby><cites>FETCH-LOGICAL-c467t-88cbbc31ffa5df2d138e0803b3c5e815b995d252c488487bd32445800c84fdf13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.polymer.2005.10.142$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17811720$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Žagar, Ema</creatorcontrib><creatorcontrib>Žigon, Majda</creatorcontrib><creatorcontrib>Podzimek, Stepan</creatorcontrib><title>Characterization of commercial aliphatic hyperbranched polyesters</title><title>Polymer (Guilford)</title><description>Commercially available Boltorn H x ( x=20, 30) hyperbranched (HB) polyesters of different theoretical core/monomer ratio (1/12 for H20 and 1/28 for H30) were characterized with respect to molar mass, composition, and structure. The results were compared to those obtained for the Boltorn H40 with a core/monomer ratio of 1/60 [Žagar E, Žigon M. Macromolecules 2002;35:9913 [11]]. The main side reaction in the pseudo one-pot synthesis of Boltorn polymers is a self-condensation of bis-MPA leading to the formation of HB structures without a core molecule. These are actually branches containing an unreacted carboxyl group. The fraction of HB structures without a core molecule increases with decreasing core/monomer ratio due to the decreasing fraction of HB structures with a core molecule. Since HB structures without a core molecule are of lower molar masses than HB structures with a core molecule, they particularly decrease the number average molar masses of the samples compared to the theoretically calculated ones. The polydispersity of Boltorn H x increases with decreasing core/monomer ratio. Some of the hydroxyl groups were found to react intramoleculary forming ether bonds. Boltorn H x polyesters have low degrees of branching due to the limited carboxyl group conversions, low DP n values, the presence of the core unit, and lower reactivity of hydroxyl groups in linear repeat units compared to those in terminal ones. The degree of branching according to Frey increases with decreasing core/monomer ratio.</description><subject>Applied sciences</subject><subject>Dendritic</subject><subject>Exact sciences and technology</subject><subject>Hyperbranched</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polyesters</subject><subject>Properties and characterization</subject><subject>Structure, morphology and analysis</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqNkEtLxDAUhYMoOI7-BKEb3bXm2aYrGQZfMOBG1yG9TWiGvkw6wvjrTZ0Bl7q6cO93zrkchK4Jzggm-d02G4d23xmfUYxFNq85PUELIguWUlqSU7TAmNGUyZyco4sQthhjKihfoNW60V7DZLz70pMb-mSwCQxddAOn20S3bmziAZJmPxpfed1DY-pkTjQhysIlOrO6DebqOJfo_fHhbf2cbl6fXtarTQo8L6ZUSqgqYMRaLWpLa8KkwRKzioEwkoiqLEUdfwIuJZdFVTPKuZAYg-S2toQt0e3Bd_TDxy5mq84FMG2rezPsgqJSCsGI_AeYl5wVLILiAIIfQvDGqtG7Tvu9IljNzaqtOjar5mZ_1pxG3c0xQAfQrZ07ceFXXEhCCoojd3_gTKzl00WXAM70YGrnDUyqHtwfSd-9Q5Iv</recordid><startdate>20060101</startdate><enddate>20060101</enddate><creator>Žagar, Ema</creator><creator>Žigon, Majda</creator><creator>Podzimek, Stepan</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope></search><sort><creationdate>20060101</creationdate><title>Characterization of commercial aliphatic hyperbranched polyesters</title><author>Žagar, Ema ; Žigon, Majda ; Podzimek, Stepan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-88cbbc31ffa5df2d138e0803b3c5e815b995d252c488487bd32445800c84fdf13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Applied sciences</topic><topic>Dendritic</topic><topic>Exact sciences and technology</topic><topic>Hyperbranched</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polyesters</topic><topic>Properties and characterization</topic><topic>Structure, morphology and analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Žagar, Ema</creatorcontrib><creatorcontrib>Žigon, Majda</creatorcontrib><creatorcontrib>Podzimek, Stepan</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Žagar, Ema</au><au>Žigon, Majda</au><au>Podzimek, Stepan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of commercial aliphatic hyperbranched polyesters</atitle><jtitle>Polymer (Guilford)</jtitle><date>2006-01-01</date><risdate>2006</risdate><volume>47</volume><issue>1</issue><spage>166</spage><epage>175</epage><pages>166-175</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>Commercially available Boltorn H x ( x=20, 30) hyperbranched (HB) polyesters of different theoretical core/monomer ratio (1/12 for H20 and 1/28 for H30) were characterized with respect to molar mass, composition, and structure. The results were compared to those obtained for the Boltorn H40 with a core/monomer ratio of 1/60 [Žagar E, Žigon M. Macromolecules 2002;35:9913 [11]]. The main side reaction in the pseudo one-pot synthesis of Boltorn polymers is a self-condensation of bis-MPA leading to the formation of HB structures without a core molecule. These are actually branches containing an unreacted carboxyl group. The fraction of HB structures without a core molecule increases with decreasing core/monomer ratio due to the decreasing fraction of HB structures with a core molecule. Since HB structures without a core molecule are of lower molar masses than HB structures with a core molecule, they particularly decrease the number average molar masses of the samples compared to the theoretically calculated ones. The polydispersity of Boltorn H x increases with decreasing core/monomer ratio. Some of the hydroxyl groups were found to react intramoleculary forming ether bonds. Boltorn H x polyesters have low degrees of branching due to the limited carboxyl group conversions, low DP n values, the presence of the core unit, and lower reactivity of hydroxyl groups in linear repeat units compared to those in terminal ones. The degree of branching according to Frey increases with decreasing core/monomer ratio.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2005.10.142</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0032-3861
ispartof Polymer (Guilford), 2006-01, Vol.47 (1), p.166-175
issn 0032-3861
1873-2291
language eng
recordid cdi_proquest_miscellaneous_28855318
source Elsevier ScienceDirect Journals
subjects Applied sciences
Dendritic
Exact sciences and technology
Hyperbranched
Organic polymers
Physicochemistry of polymers
Polyesters
Properties and characterization
Structure, morphology and analysis
title Characterization of commercial aliphatic hyperbranched polyesters
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T10%3A14%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Characterization%20of%20commercial%20aliphatic%20hyperbranched%20polyesters&rft.jtitle=Polymer%20(Guilford)&rft.au=%C5%BDagar,%20Ema&rft.date=2006-01-01&rft.volume=47&rft.issue=1&rft.spage=166&rft.epage=175&rft.pages=166-175&rft.issn=0032-3861&rft.eissn=1873-2291&rft.coden=POLMAG&rft_id=info:doi/10.1016/j.polymer.2005.10.142&rft_dat=%3Cproquest_cross%3E28694373%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=28694373&rft_id=info:pmid/&rft_els_id=S0032386105016290&rfr_iscdi=true