An Interesting Class of Porous Polymer-Revisiting the Structure of Mesoporous α-d-Polysaccharide Gels

TY - JOUR

T1 - An Interesting Class of Porous Polymer-Revisiting the Structure of Mesoporous α-d-Polysaccharide Gels

AU - White, Robin J.

AU - Shuttleworth, Peter S.

AU - Budarin, Vitaliy L.

AU - Bruyn, Mario De

AU - Fischer, Anna

AU - Clark, James H.

N1 - © 2016, Wiley-VCH Verlag GmbH & Co. K. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details.

PY - 2016/1/19

Y1 - 2016/1/19

N2 - The processes involved in the transformation of non-porous, native polysaccharides to their highly porous equivalents introduce significant molecular complexity and are not yet fully understood. In this paper, we propose that distinct changes in polysaccharide local short-range ordering promotes and directs the formation of meso- and micro-pores, which are investigated here using N2 sorption, FTIR, and solid-state 13CNMR. It is found that an increase in the overall double helical amylose content, and their local association structures, are responsible for formation of the porous polysaccharide gel phase. An exciting consequence of this local ordering change is elegantly revealed using a 19FNMR experiment, which identifies the stereochemistry-dependent diffusion of a fluorinated chiral probe molecule (1-phenyl-2,2,2-trifluoroethanol) from the meso- to the micro-pore region. This finding opens opportunities in the area of polysaccharide-based chiral stationary phases and asymmetric catalyst preparation.

AB - The processes involved in the transformation of non-porous, native polysaccharides to their highly porous equivalents introduce significant molecular complexity and are not yet fully understood. In this paper, we propose that distinct changes in polysaccharide local short-range ordering promotes and directs the formation of meso- and micro-pores, which are investigated here using N2 sorption, FTIR, and solid-state 13CNMR. It is found that an increase in the overall double helical amylose content, and their local association structures, are responsible for formation of the porous polysaccharide gel phase. An exciting consequence of this local ordering change is elegantly revealed using a 19FNMR experiment, which identifies the stereochemistry-dependent diffusion of a fluorinated chiral probe molecule (1-phenyl-2,2,2-trifluoroethanol) from the meso- to the micro-pore region. This finding opens opportunities in the area of polysaccharide-based chiral stationary phases and asymmetric catalyst preparation.

KW - Chiral

KW - Diffusion

KW - Polysaccharides

KW - Porosity

KW - Xerogels

UR - http://www.scopus.com/inward/record.url?scp=84956858703&partnerID=8YFLogxK

U2 - 10.1002/cssc.201501354

DO - 10.1002/cssc.201501354

M3 - Article

AN - SCOPUS:84956858703

VL - 9

SP - 280

EP - 288

JO - ChemSusChem

JF - ChemSusChem

SN - 1864-5631

IS - 3

ER -