Loading…

First multi-reactive dextran-based inisurf for atom transfer radical polymerization in miniemulsion

•Dextran-based inisurfs (acting both as initiator and stabilizer) are synthesized•Surface active properties of inisurfs similar to amphiphilic dextran derivatives•Miniemulsion AGET–ATRP of BA is optimized with model initiator and inisiurf•ATRP groups are in contact with oil/monomer interface and ini...

Full description

Saved in:
Bibliographic Details
Published in:Carbohydrate polymers 2015-10, Vol.130, p.141-148
Main Authors: Wu, Man, Forero Ramirez, Laura M., Rodriguez Lozano, Ana, Quémener, Damien, Babin, Jérôme, Durand, Alain, Marie, Emmanuelle, Six, Jean-Luc, Nouvel, Cécile
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c399t-ec629da4b2a133428e000598c2912a725e8e975c49d178ac5918237b78caf3ac3
cites cdi_FETCH-LOGICAL-c399t-ec629da4b2a133428e000598c2912a725e8e975c49d178ac5918237b78caf3ac3
container_end_page 148
container_issue
container_start_page 141
container_title Carbohydrate polymers
container_volume 130
creator Wu, Man
Forero Ramirez, Laura M.
Rodriguez Lozano, Ana
Quémener, Damien
Babin, Jérôme
Durand, Alain
Marie, Emmanuelle
Six, Jean-Luc
Nouvel, Cécile
description •Dextran-based inisurfs (acting both as initiator and stabilizer) are synthesized•Surface active properties of inisurfs similar to amphiphilic dextran derivatives•Miniemulsion AGET–ATRP of BA is optimized with model initiator and inisiurf•ATRP groups are in contact with oil/monomer interface and initiate polymerization•Kinetics and nanoparticle characteristics are correlated to experimental conditions A multi-reactive polysaccharide-based inisurf (acting both as initiator and stabilizer) has been designed for the first time from dextran with the aim of preparing dextran-covered nanoparticles with covalent linkage between core and coverage. This inisurf was used for polymerizing butyl acrylate in miniemulsion by AGET–ATRP. Both hydrophobic phenoxy groups and initiator groups (bromoisobutyryl ester) were introduced within hydrophilic dextran chain, conferring it amphiphilic and macroinitiator characters. Amphiphilic properties of dextran inisurfs have been evidenced as well as their ability to stabilize the direct miniemulsion of n-butyl acrylate. After optimization of polymerization conditions with model studies, assays were successfully realized with dextran-based inisurfs. Because of their amphiphilic character, inisurfs migrated at oil/water interface and initiated polymerization from bromoisobutyryl ester groups. Therefore graft copolymers were produced at oil/water interface, due to the multifunctional character of these inisurfs and constituted the particle inner core with covalent links to the dextran coverage.
doi_str_mv 10.1016/j.carbpol.2015.05.002
format article
fullrecord <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_01497729v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0144861715004002</els_id><sourcerecordid>1689621702</sourcerecordid><originalsourceid>FETCH-LOGICAL-c399t-ec629da4b2a133428e000598c2912a725e8e975c49d178ac5918237b78caf3ac3</originalsourceid><addsrcrecordid>eNqFUU2LFDEQDaK44-pPUHLUQ4-p9EeSkyyL6woDXvQcqtPVmKG7Mybpwd1fb8YZ92ooyNd7r4r3GHsLYgsCuo_7rcPYH8K0lQLarSgl5DO2Aa1MBXXTPGcbAU1T6Q7UFXuV0l6U1YF4ya5kJ1RXjhvm7nxMmc_rlH0VCV32R-ID_c4Rl6rHRAP3i09rHPkYIsccZn76SyNFHnHwDidexniYKfpHzD4shcDnQqKimsr9NXsx4pTozWW_Zj_uPn-_va923758vb3ZVa42JlfkOmkGbHqJUNeN1FTmbY120oBEJVvSZFTrGjOA0uhaA1rWqlfa4Vijq6_Zh7PuT5zsIfoZ44MN6O39zc6e3oofRilpjlCw78_YQwy_VkrZzj45miZcKKzJQqdNJ0EJWaDtGepiSCnS-KQNwp6ysHt7ycKesrCi1F_eu0uLtZ9peGL9M78APp0BVEw5eoo2OU-Lo8FHctkOwf-nxR_VX520</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1689621702</pqid></control><display><type>article</type><title>First multi-reactive dextran-based inisurf for atom transfer radical polymerization in miniemulsion</title><source>ScienceDirect Journals</source><creator>Wu, Man ; Forero Ramirez, Laura M. ; Rodriguez Lozano, Ana ; Quémener, Damien ; Babin, Jérôme ; Durand, Alain ; Marie, Emmanuelle ; Six, Jean-Luc ; Nouvel, Cécile</creator><creatorcontrib>Wu, Man ; Forero Ramirez, Laura M. ; Rodriguez Lozano, Ana ; Quémener, Damien ; Babin, Jérôme ; Durand, Alain ; Marie, Emmanuelle ; Six, Jean-Luc ; Nouvel, Cécile</creatorcontrib><description>•Dextran-based inisurfs (acting both as initiator and stabilizer) are synthesized•Surface active properties of inisurfs similar to amphiphilic dextran derivatives•Miniemulsion AGET–ATRP of BA is optimized with model initiator and inisiurf•ATRP groups are in contact with oil/monomer interface and initiate polymerization•Kinetics and nanoparticle characteristics are correlated to experimental conditions A multi-reactive polysaccharide-based inisurf (acting both as initiator and stabilizer) has been designed for the first time from dextran with the aim of preparing dextran-covered nanoparticles with covalent linkage between core and coverage. This inisurf was used for polymerizing butyl acrylate in miniemulsion by AGET–ATRP. Both hydrophobic phenoxy groups and initiator groups (bromoisobutyryl ester) were introduced within hydrophilic dextran chain, conferring it amphiphilic and macroinitiator characters. Amphiphilic properties of dextran inisurfs have been evidenced as well as their ability to stabilize the direct miniemulsion of n-butyl acrylate. After optimization of polymerization conditions with model studies, assays were successfully realized with dextran-based inisurfs. Because of their amphiphilic character, inisurfs migrated at oil/water interface and initiated polymerization from bromoisobutyryl ester groups. Therefore graft copolymers were produced at oil/water interface, due to the multifunctional character of these inisurfs and constituted the particle inner core with covalent links to the dextran coverage.</description><identifier>ISSN: 0144-8617</identifier><identifier>EISSN: 1879-1344</identifier><identifier>DOI: 10.1016/j.carbpol.2015.05.002</identifier><identifier>PMID: 26076610</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>AGET ; Chemical Sciences ; Dextrans - chemistry ; Emulsions - chemistry ; Glycopolymer ; Hydrophobic and Hydrophilic Interactions ; Kinetics ; Magnetic Resonance Spectroscopy ; Nanoparticle ; Nanoparticles - chemistry ; Organic chemistry ; Polymerization ; Polymers ; Polysaccharide ; Reversible-deactivation radical polymerization ; Surface Properties ; Surface-Active Agents - chemistry ; Surfactant</subject><ispartof>Carbohydrate polymers, 2015-10, Vol.130, p.141-148</ispartof><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-ec629da4b2a133428e000598c2912a725e8e975c49d178ac5918237b78caf3ac3</citedby><cites>FETCH-LOGICAL-c399t-ec629da4b2a133428e000598c2912a725e8e975c49d178ac5918237b78caf3ac3</cites><orcidid>0000-0002-4154-187X ; 0000-0001-9275-5707 ; 0000-0001-9522-3781 ; 0000-0003-1151-6953 ; 0000-0003-3800-6769</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26076610$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.univ-lorraine.fr/hal-01497729$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Man</creatorcontrib><creatorcontrib>Forero Ramirez, Laura M.</creatorcontrib><creatorcontrib>Rodriguez Lozano, Ana</creatorcontrib><creatorcontrib>Quémener, Damien</creatorcontrib><creatorcontrib>Babin, Jérôme</creatorcontrib><creatorcontrib>Durand, Alain</creatorcontrib><creatorcontrib>Marie, Emmanuelle</creatorcontrib><creatorcontrib>Six, Jean-Luc</creatorcontrib><creatorcontrib>Nouvel, Cécile</creatorcontrib><title>First multi-reactive dextran-based inisurf for atom transfer radical polymerization in miniemulsion</title><title>Carbohydrate polymers</title><addtitle>Carbohydr Polym</addtitle><description>•Dextran-based inisurfs (acting both as initiator and stabilizer) are synthesized•Surface active properties of inisurfs similar to amphiphilic dextran derivatives•Miniemulsion AGET–ATRP of BA is optimized with model initiator and inisiurf•ATRP groups are in contact with oil/monomer interface and initiate polymerization•Kinetics and nanoparticle characteristics are correlated to experimental conditions A multi-reactive polysaccharide-based inisurf (acting both as initiator and stabilizer) has been designed for the first time from dextran with the aim of preparing dextran-covered nanoparticles with covalent linkage between core and coverage. This inisurf was used for polymerizing butyl acrylate in miniemulsion by AGET–ATRP. Both hydrophobic phenoxy groups and initiator groups (bromoisobutyryl ester) were introduced within hydrophilic dextran chain, conferring it amphiphilic and macroinitiator characters. Amphiphilic properties of dextran inisurfs have been evidenced as well as their ability to stabilize the direct miniemulsion of n-butyl acrylate. After optimization of polymerization conditions with model studies, assays were successfully realized with dextran-based inisurfs. Because of their amphiphilic character, inisurfs migrated at oil/water interface and initiated polymerization from bromoisobutyryl ester groups. Therefore graft copolymers were produced at oil/water interface, due to the multifunctional character of these inisurfs and constituted the particle inner core with covalent links to the dextran coverage.</description><subject>AGET</subject><subject>Chemical Sciences</subject><subject>Dextrans - chemistry</subject><subject>Emulsions - chemistry</subject><subject>Glycopolymer</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Kinetics</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Nanoparticle</subject><subject>Nanoparticles - chemistry</subject><subject>Organic chemistry</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Polysaccharide</subject><subject>Reversible-deactivation radical polymerization</subject><subject>Surface Properties</subject><subject>Surface-Active Agents - chemistry</subject><subject>Surfactant</subject><issn>0144-8617</issn><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFUU2LFDEQDaK44-pPUHLUQ4-p9EeSkyyL6woDXvQcqtPVmKG7Mybpwd1fb8YZ92ooyNd7r4r3GHsLYgsCuo_7rcPYH8K0lQLarSgl5DO2Aa1MBXXTPGcbAU1T6Q7UFXuV0l6U1YF4ya5kJ1RXjhvm7nxMmc_rlH0VCV32R-ID_c4Rl6rHRAP3i09rHPkYIsccZn76SyNFHnHwDidexniYKfpHzD4shcDnQqKimsr9NXsx4pTozWW_Zj_uPn-_va923758vb3ZVa42JlfkOmkGbHqJUNeN1FTmbY120oBEJVvSZFTrGjOA0uhaA1rWqlfa4Vijq6_Zh7PuT5zsIfoZ44MN6O39zc6e3oofRilpjlCw78_YQwy_VkrZzj45miZcKKzJQqdNJ0EJWaDtGepiSCnS-KQNwp6ysHt7ycKesrCi1F_eu0uLtZ9peGL9M78APp0BVEw5eoo2OU-Lo8FHctkOwf-nxR_VX520</recordid><startdate>20151005</startdate><enddate>20151005</enddate><creator>Wu, Man</creator><creator>Forero Ramirez, Laura M.</creator><creator>Rodriguez Lozano, Ana</creator><creator>Quémener, Damien</creator><creator>Babin, Jérôme</creator><creator>Durand, Alain</creator><creator>Marie, Emmanuelle</creator><creator>Six, Jean-Luc</creator><creator>Nouvel, Cécile</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-4154-187X</orcidid><orcidid>https://orcid.org/0000-0001-9275-5707</orcidid><orcidid>https://orcid.org/0000-0001-9522-3781</orcidid><orcidid>https://orcid.org/0000-0003-1151-6953</orcidid><orcidid>https://orcid.org/0000-0003-3800-6769</orcidid></search><sort><creationdate>20151005</creationdate><title>First multi-reactive dextran-based inisurf for atom transfer radical polymerization in miniemulsion</title><author>Wu, Man ; Forero Ramirez, Laura M. ; Rodriguez Lozano, Ana ; Quémener, Damien ; Babin, Jérôme ; Durand, Alain ; Marie, Emmanuelle ; Six, Jean-Luc ; Nouvel, Cécile</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-ec629da4b2a133428e000598c2912a725e8e975c49d178ac5918237b78caf3ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>AGET</topic><topic>Chemical Sciences</topic><topic>Dextrans - chemistry</topic><topic>Emulsions - chemistry</topic><topic>Glycopolymer</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Kinetics</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Nanoparticle</topic><topic>Nanoparticles - chemistry</topic><topic>Organic chemistry</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Polysaccharide</topic><topic>Reversible-deactivation radical polymerization</topic><topic>Surface Properties</topic><topic>Surface-Active Agents - chemistry</topic><topic>Surfactant</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Man</creatorcontrib><creatorcontrib>Forero Ramirez, Laura M.</creatorcontrib><creatorcontrib>Rodriguez Lozano, Ana</creatorcontrib><creatorcontrib>Quémener, Damien</creatorcontrib><creatorcontrib>Babin, Jérôme</creatorcontrib><creatorcontrib>Durand, Alain</creatorcontrib><creatorcontrib>Marie, Emmanuelle</creatorcontrib><creatorcontrib>Six, Jean-Luc</creatorcontrib><creatorcontrib>Nouvel, Cécile</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Man</au><au>Forero Ramirez, Laura M.</au><au>Rodriguez Lozano, Ana</au><au>Quémener, Damien</au><au>Babin, Jérôme</au><au>Durand, Alain</au><au>Marie, Emmanuelle</au><au>Six, Jean-Luc</au><au>Nouvel, Cécile</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First multi-reactive dextran-based inisurf for atom transfer radical polymerization in miniemulsion</atitle><jtitle>Carbohydrate polymers</jtitle><addtitle>Carbohydr Polym</addtitle><date>2015-10-05</date><risdate>2015</risdate><volume>130</volume><spage>141</spage><epage>148</epage><pages>141-148</pages><issn>0144-8617</issn><eissn>1879-1344</eissn><abstract>•Dextran-based inisurfs (acting both as initiator and stabilizer) are synthesized•Surface active properties of inisurfs similar to amphiphilic dextran derivatives•Miniemulsion AGET–ATRP of BA is optimized with model initiator and inisiurf•ATRP groups are in contact with oil/monomer interface and initiate polymerization•Kinetics and nanoparticle characteristics are correlated to experimental conditions A multi-reactive polysaccharide-based inisurf (acting both as initiator and stabilizer) has been designed for the first time from dextran with the aim of preparing dextran-covered nanoparticles with covalent linkage between core and coverage. This inisurf was used for polymerizing butyl acrylate in miniemulsion by AGET–ATRP. Both hydrophobic phenoxy groups and initiator groups (bromoisobutyryl ester) were introduced within hydrophilic dextran chain, conferring it amphiphilic and macroinitiator characters. Amphiphilic properties of dextran inisurfs have been evidenced as well as their ability to stabilize the direct miniemulsion of n-butyl acrylate. After optimization of polymerization conditions with model studies, assays were successfully realized with dextran-based inisurfs. Because of their amphiphilic character, inisurfs migrated at oil/water interface and initiated polymerization from bromoisobutyryl ester groups. Therefore graft copolymers were produced at oil/water interface, due to the multifunctional character of these inisurfs and constituted the particle inner core with covalent links to the dextran coverage.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26076610</pmid><doi>10.1016/j.carbpol.2015.05.002</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4154-187X</orcidid><orcidid>https://orcid.org/0000-0001-9275-5707</orcidid><orcidid>https://orcid.org/0000-0001-9522-3781</orcidid><orcidid>https://orcid.org/0000-0003-1151-6953</orcidid><orcidid>https://orcid.org/0000-0003-3800-6769</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0144-8617
ispartof Carbohydrate polymers, 2015-10, Vol.130, p.141-148
issn 0144-8617
1879-1344
language eng
recordid cdi_hal_primary_oai_HAL_hal_01497729v1
source ScienceDirect Journals
subjects AGET
Chemical Sciences
Dextrans - chemistry
Emulsions - chemistry
Glycopolymer
Hydrophobic and Hydrophilic Interactions
Kinetics
Magnetic Resonance Spectroscopy
Nanoparticle
Nanoparticles - chemistry
Organic chemistry
Polymerization
Polymers
Polysaccharide
Reversible-deactivation radical polymerization
Surface Properties
Surface-Active Agents - chemistry
Surfactant
title First multi-reactive dextran-based inisurf for atom transfer radical polymerization in miniemulsion
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T11%3A17%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=First%20multi-reactive%20dextran-based%20inisurf%20for%20atom%20transfer%20radical%20polymerization%20in%20miniemulsion&rft.jtitle=Carbohydrate%20polymers&rft.au=Wu,%20Man&rft.date=2015-10-05&rft.volume=130&rft.spage=141&rft.epage=148&rft.pages=141-148&rft.issn=0144-8617&rft.eissn=1879-1344&rft_id=info:doi/10.1016/j.carbpol.2015.05.002&rft_dat=%3Cproquest_hal_p%3E1689621702%3C/proquest_hal_p%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c399t-ec629da4b2a133428e000598c2912a725e8e975c49d178ac5918237b78caf3ac3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1689621702&rft_id=info:pmid/26076610&rfr_iscdi=true