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Pyrene End-Labeled Diblock Glycopolymers: Synthesis and Aggregation
A pyrene end‐labeled amphiphilic block copolymer, poly(ε‐caprolactone)‐block‐poly[6‐O‐(4‐vinylbenzyl)‐D‐galactose] (Py‐PCL‐b‐PVBG), was synthesized by a four‐step method. The aggregation behavior of the diblock copolymer in solution was studied by monitoring the fluorescence of pyrene. TEM measureme...
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Published in: | Macromolecular chemistry and physics 2005-02, Vol.206 (4), p.513-520 |
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creator | Lu, Feng-Zhu Meng, Jian-Qiang Du, Fu-Sheng Li, Zi-Chen Zhang, Bao-Yan |
description | A pyrene end‐labeled amphiphilic block copolymer, poly(ε‐caprolactone)‐block‐poly[6‐O‐(4‐vinylbenzyl)‐D‐galactose] (Py‐PCL‐b‐PVBG), was synthesized by a four‐step method. The aggregation behavior of the diblock copolymer in solution was studied by monitoring the fluorescence of pyrene. TEM measurements revealed that the aggregates obtained by first dissolving the copolymer in N,N‐dimethylformamide (DMF), followed by the addition of water, were primarily spheres with the PCL blocks in the core. The PVBG corona was then crosslinked with glutaraldehyde. Final removal of the PCL core was accomplished by degradation under basic conditions, which resulted in the formation of hollow glycopolymer nanospheres.
Structure of poly(ε‐caprolactone)‐block‐poly[6‐O‐(4‐vinylbenzyl)‐D‐galactose]. |
doi_str_mv | 10.1002/macp.200400354 |
format | article |
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Structure of poly(ε‐caprolactone)‐block‐poly[6‐O‐(4‐vinylbenzyl)‐D‐galactose].</description><identifier>ISSN: 1022-1352</identifier><identifier>EISSN: 1521-3935</identifier><identifier>DOI: 10.1002/macp.200400354</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>block copolymers ; crosslinking ; fluorescence ; glycopolymer ; self-assembly</subject><ispartof>Macromolecular chemistry and physics, 2005-02, Vol.206 (4), p.513-520</ispartof><rights>Copyright © 2005 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3934-183e60199c81e471e977721e5be4d72561856e6ad9fa41428b9ebd6450f6da3d3</citedby><cites>FETCH-LOGICAL-c3934-183e60199c81e471e977721e5be4d72561856e6ad9fa41428b9ebd6450f6da3d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Lu, Feng-Zhu</creatorcontrib><creatorcontrib>Meng, Jian-Qiang</creatorcontrib><creatorcontrib>Du, Fu-Sheng</creatorcontrib><creatorcontrib>Li, Zi-Chen</creatorcontrib><creatorcontrib>Zhang, Bao-Yan</creatorcontrib><title>Pyrene End-Labeled Diblock Glycopolymers: Synthesis and Aggregation</title><title>Macromolecular chemistry and physics</title><addtitle>Macromol. Chem. Phys</addtitle><description>A pyrene end‐labeled amphiphilic block copolymer, poly(ε‐caprolactone)‐block‐poly[6‐O‐(4‐vinylbenzyl)‐D‐galactose] (Py‐PCL‐b‐PVBG), was synthesized by a four‐step method. The aggregation behavior of the diblock copolymer in solution was studied by monitoring the fluorescence of pyrene. TEM measurements revealed that the aggregates obtained by first dissolving the copolymer in N,N‐dimethylformamide (DMF), followed by the addition of water, were primarily spheres with the PCL blocks in the core. The PVBG corona was then crosslinked with glutaraldehyde. Final removal of the PCL core was accomplished by degradation under basic conditions, which resulted in the formation of hollow glycopolymer nanospheres.
Structure of poly(ε‐caprolactone)‐block‐poly[6‐O‐(4‐vinylbenzyl)‐D‐galactose].</description><subject>block copolymers</subject><subject>crosslinking</subject><subject>fluorescence</subject><subject>glycopolymer</subject><subject>self-assembly</subject><issn>1022-1352</issn><issn>1521-3935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkE1PwkAURSdGExHduu4fKL756nTckQpogkqCBnaTaecVK6UlMyTafy8EQ9y5enfxzs3NIeSWwoACsLuNLbYDBiAAuBRnpEclozHXXJ7vMzAWUy7ZJbkK4RMAUtCqR7JZ57HBaNS4eGpzrNFFD1Vet8U6mtRd0W7butugD_fRvGt2HxiqENnGRcPVyuPK7qq2uSYXpa0D3vzePnkfj96yx3j6OnnKhtO42I8QMU05JkC1LlKKQlHUSilGUeYonGIyoalMMLFOl1ZQwdJcY-4SIaFMnOWO98ng2Fv4NgSPpdn6amN9ZyiYgwJzUGBOCvaAPgJfVY3dP9_meZjN_rLxka3CDr9PrPVrkyiupFm8TMx8MXteSj42S_4D2RRuwg</recordid><startdate>20050221</startdate><enddate>20050221</enddate><creator>Lu, Feng-Zhu</creator><creator>Meng, Jian-Qiang</creator><creator>Du, Fu-Sheng</creator><creator>Li, Zi-Chen</creator><creator>Zhang, Bao-Yan</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050221</creationdate><title>Pyrene End-Labeled Diblock Glycopolymers: Synthesis and Aggregation</title><author>Lu, Feng-Zhu ; Meng, Jian-Qiang ; Du, Fu-Sheng ; Li, Zi-Chen ; Zhang, Bao-Yan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3934-183e60199c81e471e977721e5be4d72561856e6ad9fa41428b9ebd6450f6da3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>block copolymers</topic><topic>crosslinking</topic><topic>fluorescence</topic><topic>glycopolymer</topic><topic>self-assembly</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Feng-Zhu</creatorcontrib><creatorcontrib>Meng, Jian-Qiang</creatorcontrib><creatorcontrib>Du, Fu-Sheng</creatorcontrib><creatorcontrib>Li, Zi-Chen</creatorcontrib><creatorcontrib>Zhang, Bao-Yan</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Macromolecular chemistry and physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Feng-Zhu</au><au>Meng, Jian-Qiang</au><au>Du, Fu-Sheng</au><au>Li, Zi-Chen</au><au>Zhang, Bao-Yan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyrene End-Labeled Diblock Glycopolymers: Synthesis and Aggregation</atitle><jtitle>Macromolecular chemistry and physics</jtitle><addtitle>Macromol. Chem. Phys</addtitle><date>2005-02-21</date><risdate>2005</risdate><volume>206</volume><issue>4</issue><spage>513</spage><epage>520</epage><pages>513-520</pages><issn>1022-1352</issn><eissn>1521-3935</eissn><abstract>A pyrene end‐labeled amphiphilic block copolymer, poly(ε‐caprolactone)‐block‐poly[6‐O‐(4‐vinylbenzyl)‐D‐galactose] (Py‐PCL‐b‐PVBG), was synthesized by a four‐step method. The aggregation behavior of the diblock copolymer in solution was studied by monitoring the fluorescence of pyrene. TEM measurements revealed that the aggregates obtained by first dissolving the copolymer in N,N‐dimethylformamide (DMF), followed by the addition of water, were primarily spheres with the PCL blocks in the core. The PVBG corona was then crosslinked with glutaraldehyde. Final removal of the PCL core was accomplished by degradation under basic conditions, which resulted in the formation of hollow glycopolymer nanospheres.
Structure of poly(ε‐caprolactone)‐block‐poly[6‐O‐(4‐vinylbenzyl)‐D‐galactose].</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/macp.200400354</doi><tpages>8</tpages></addata></record> |
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source | Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list) |
subjects | block copolymers crosslinking fluorescence glycopolymer self-assembly |
title | Pyrene End-Labeled Diblock Glycopolymers: Synthesis and Aggregation |
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