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dc.rights.licenseembargoen_US
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorSOLBERG, Amalie
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorMO, Ingrid V.
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorOMTVEDT, Line A.-A.
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorSTRAND, Berit L.
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorAACHMANN, Finn L.
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.accessioned2022-01-06T16:48:42Z
dc.date.available2022-01-06T16:48:42Z
dc.date.issued2022-02-15
dc.identifier.issn0144-8617en_US
dc.identifier.urioai:crossref.org:10.1016/j.carbpol.2021.118840
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124333
dc.description.abstractEnEngineered block polysaccharides is a relatively new class of biomacromolecules consisting of chemical assembly of separate block structures at the chain termini. In contrast to conventional, laterally substituted polysaccharide derivatives, the block arrangement allows for much higher preservation of inherent chain properties such as biodegradability and stimuli-responsive self-assembly, while at the same time inducing new macromolecular properties. Abundant, carbon neutral, and even recalcitrant biomass is an excellent source of blocks, opening for numerous new uses of biomass for a wide range of novel biomaterials. Among a limited range of methodologies available for block conjugation, bifunctional linkers allowing for oxyamine and hydrazide ‘click’ reactions have recently proven useful additions to the repertoire. This article focuses the chemistry and kinetics of these reactions. It also presents some new data with the aim to provide useful protocols and methods for general use towards new block polysaccharides.
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.enCarbohydr Polym Special Issue Invited contribution: Click chemistry for block polysaccharides with dihydrazide and dioxyamine linkers - A review
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.carbpol.2021.118840en_US
dc.subject.halChimie/Polymèresen_US
dc.identifier.pubmed34973722en_US
bordeaux.journalCarbohydrate Polymersen_US
bordeaux.page118840en_US
bordeaux.volume278en_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-03515520
hal.version1
hal.date.transferred2022-01-06T16:48:45Z
hal.exporttrue
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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=2022-02-15&rft.volume=278&rft.spage=118840&rft.epage=118840&rft.eissn=0144-8617&rft.issn=0144-8617&rft.au=SOLBERG,%20Amalie&MO,%20Ingrid%20V.&OMTVEDT,%20Line%20A.-A.&STRAND,%20Berit%20L.&AACHMANN,%20Finn%20L.&rft.genre=article


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