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dc.rights.licenseopenen_US
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorMO, Ingrid Vikøren
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorSCHATZ, Christophe
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorCHRISTENSEN, Bjørn E.
dc.date.accessioned2022-01-04T18:58:07Z
dc.date.available2022-01-04T18:58:07Z
dc.date.issued2021-05-13
dc.identifier.issn0144-8617en_US
dc.identifier.urioai:crossref.org:10.1016/j.carbpol.2021.118193
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124316
dc.description.abstractEnMost polysaccharides used in polysaccharide-based block copolymers are attached to the second block through the reducing end, due to the few and highly polysaccharide specific non-reducing end (NRE) functionalisation methods available. Chitin oligomers, prepared by nitrous acid degradation of chitosan (AnM) can, however, be selectively oxidised by periodate since they only possess a single vicinal diol in the NRE residue. Here, we show that both aldehydes formed after oxidation are highly reactive towards bifunctional oxyamines and hydrazide linkers. Sub-stochiometric amounts of linkers resulted in conjugation of AnM oligomers through both chain termini to yield a discrete distribution of ‘polymerised’ oligomers. Such chitin-based block polymers were, in contrast to chitins of the same chain lengths, water-soluble. Oxidised AnM oligomers, functionalised at both termini can also enable the preparation of more complex block polysaccharides such as ABA- or ABC-type.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.sourcecrossref
dc.title.enFunctionalisation of the non-reducing end of chitin by selective periodate oxidation: A new approach to form complex block polysaccharides and water-soluble chitin-based block polymers
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.carbpol.2021.118193en_US
dc.subject.halChimie/Polymèresen_US
dc.identifier.pubmed34119160en_US
bordeaux.journalCarbohydrate Polymersen_US
bordeaux.page118193en_US
bordeaux.volume267en_US
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-03511293
hal.version1
hal.date.transferred2022-01-04T18:58:12Z
hal.exporttrue
workflow.import.sourcedissemin
dc.rights.ccCC BY-NC-SAen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Carbohydrate%20Polymers&rft.date=2021-05-13&rft.volume=267&rft.spage=118193&rft.epage=118193&rft.eissn=0144-8617&rft.issn=0144-8617&rft.au=MO,%20Ingrid%20Vik%C3%B8ren&SCHATZ,%20Christophe&CHRISTENSEN,%20Bj%C3%B8rn%20E.&rft.genre=article


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