TY - JOUR
T1 - Assembling Native Elementary Cellulose Nanofibrils via a Reversible and Regioselective Surface Functionalization
AU - Beaumont, Marco
AU - Tardy, Blaise
AU - Reyes, Guillermo
AU - Koso, Tetyana
AU - Schaubmayr, Elisabeth
AU - Jusner, Paul
AU - King, Alistair
AU - Dagastine, Raymond
AU - Potthast, Antje
AU - Rojas, Orlando J.
AU - Rosenau, Thomas
PY - 2021/10/20
Y1 - 2021/10/20
N2 - Selective surface modification of biobased fibers affords effective individualization and functionalization into nanomaterials, as exemplified by the TEMPO-mediated oxidation. However, such a route leads to changes of the native surface chemistry, affecting interparticle interactions and limiting the development of potential supermaterials. Here we introduce a methodology to extract elementary cellulose fibrils by treatment of biomass with N-succinylimidazole, achieving regioselective surface modification of C6-OH, which can be reverted using mild post-treatments. No polymer degradation, cross-linking, nor changes in crystallinity occur under the mild processing conditions, yielding cellulose nanofibrils bearing carboxyl moieties, which can be removed by saponification. The latter offers a significant opportunity in the reconstitution of the chemical and structural interfaces associated with the native states. Consequently, 3D structuring of native elementary cellulose nanofibrils is made possible with the same supramolecular features as the biosynthesized fibers, which is required to unlock the full potential of cellulose as a sustainable building block.
AB - Selective surface modification of biobased fibers affords effective individualization and functionalization into nanomaterials, as exemplified by the TEMPO-mediated oxidation. However, such a route leads to changes of the native surface chemistry, affecting interparticle interactions and limiting the development of potential supermaterials. Here we introduce a methodology to extract elementary cellulose fibrils by treatment of biomass with N-succinylimidazole, achieving regioselective surface modification of C6-OH, which can be reverted using mild post-treatments. No polymer degradation, cross-linking, nor changes in crystallinity occur under the mild processing conditions, yielding cellulose nanofibrils bearing carboxyl moieties, which can be removed by saponification. The latter offers a significant opportunity in the reconstitution of the chemical and structural interfaces associated with the native states. Consequently, 3D structuring of native elementary cellulose nanofibrils is made possible with the same supramolecular features as the biosynthesized fibers, which is required to unlock the full potential of cellulose as a sustainable building block.
KW - 116 Chemical sciences
KW - ELASTIC-MODULUS
KW - OXIDATION
U2 - 10.1021/jacs.1c06502
DO - 10.1021/jacs.1c06502
M3 - Article
VL - 143
SP - 17040
EP - 17046
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 41
ER -