Show simple item record

dc.contributor.authorSolberg, Amalie
dc.contributor.authorVikøren Mo, Ingrid
dc.contributor.authorOmtvedt, Line Aa.
dc.contributor.authorStrand, Berit L.
dc.contributor.authorAachmann, Finn L.
dc.contributor.authorSchatz, Christophe
dc.contributor.authorChristensen, Bjørn E.
dc.description.abstractEngineered 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.en_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.titleClick chemistry for block polysaccharides with dihydrazide and dioxyamine linkers - A reviewen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.source.journalCarbohydrate Polymersen_US
dc.description.localcodeThis is the authors' accepted manuscript to an article published by Elsevier. Locked until 8/11-2022 due to copyright restrictions. The AAM is made available under the CC-BY-NC-ND 4.0 license

Files in this item


This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal