Stereochemistry-dependent thermotropic liquid crystalline phases of monosaccharide-based amphiphiles

Author:

Mattsson Ida1,Majoinen Johanna23ORCID,Lahtinen Manu4ORCID,Sandberg Thomas1ORCID,Fogde Anna1,Saloranta-Simell Tiina1,Rojas Orlando J.25,Ikkala Olli6ORCID,Leino Reko1ORCID

Affiliation:

1. Laboratory of Molecular Science and Engineering, Johan Gadolin Process Chemistry Centre, Åbo Akademi University, FI-20500, Finland

2. Department of Bioproducts and Biosystems, School of Chemical Engineering, Aalto University, FI-00076 Aalto, Finland

3. VTT Technical Research Centre of Finland Ltd, FI-02150, Finland

4. Department of Chemistry, University of Jyväskylä, FI-40014, Finland

5. Bioproducts Institute, Department of Chemical and Biological Engineering, Department of Chemistry and Department of Wood Science, University of British Columbia, 2360 East Mall, Vancouver, BC V6T 1Z4, Canada

6. Department of Applied Physics, Aalto University, Espoo FI-00076, Finland

Abstract

Stereochemistry of glyco-based high-χ block molecules should not be neglected in their assemblies in materials design, especially at the interfaces between the nanophase segregated domains, to master the structural complexity.

Funder

Canada Excellence Research Chairs, Government of Canada

Canada Foundation for Innovation

H2020 European Research Council

Academy of Finland

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Chemistry

Reference83 articles.

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2. O.Ikkala , N.Houbenov and P.Rannou , in Handbook of Liquid Crystals , ed. P. Goodby , J. W. Collings , P. J. Kato , T. Tschierske , C. Gleeson and H. Raynes , Wiley-VCH Verlag GmbH & Co , Series Eds., 2014 , pp. 541–598

3. Self-Assembly: From Surfactants to Nanoparticles , ed. R. Nagarajan , Wiley , 2018

4. Properties and applications of precision oligomer materials; where organic and polymer chemistry join forces

5. Theory of Microphase Separation in Block Copolymers

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