dc.contributor.author
Fittolani, Giulio
dc.contributor.author
Djalali, Surusch
dc.contributor.author
Chaube, Manishkumar A.
dc.contributor.author
Tyrikos-Ergas, Theodore
dc.contributor.author
Dal Colle, Marlene C. S.
dc.contributor.author
Grafmüller, Andrea
dc.contributor.author
Seeberger, Peter H.
dc.contributor.author
Delbianco, Martina
dc.date.accessioned
2023-01-09T13:31:36Z
dc.date.available
2023-01-09T13:31:36Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/37538
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-37252
dc.description.abstract
Cellulose and chitin are abundant structural polysaccharides exploited by nature in a large number of applications thanks to their crystallinity. Chemical modifications are commonly employed to tune polysaccharide physical and mechanical properties, but generate heterogeneous mixtures. Thus, the effect of such modifications is not well understood at the molecular level. In this work, we examined how deoxyfluorination (site and pattern) impact the solubility and aggregation of well-defined cellulose and chitin oligomers. While deoxyfluorination increased solubility in water and lowered the crystallinity of cellulose oligomers, chitin was much less affected by the modification. The OH/F substitution also highlighted the role of specific hydroxyl groups in the crystallization process. This work provides guidelines for the design of cellulose- and chitin-based materials. A similar approach can be imagined to prepare cellulose and chitin analogues capable of withstanding enzymatic degradation.
en
dc.format.extent
8 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
polysaccharides
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften
dc.title
Deoxyfluorination tunes the aggregation of cellulose and chitin oligosaccharides and highlights the role of specific hydroxyl groups in the crystallization process
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1039/D2OB01601J
dcterms.bibliographicCitation.journaltitle
Organic & Biomolecular Chemistry
dcterms.bibliographicCitation.number
42
dcterms.bibliographicCitation.pagestart
8228
dcterms.bibliographicCitation.pageend
8235
dcterms.bibliographicCitation.volume
20
dcterms.bibliographicCitation.url
https://doi.org/10.1039/D2OB01601J
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1477-0539
refubium.resourceType.provider
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