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      Poly(alkanoyl isosorbide methacrylate)s: From Amorphous to Semicrystalline and Liquid Crystalline Biobased Materials

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          Abstract

          We have prepared a series of 12 d-isosorbide-2-alkanoate-5-methacrylate monomers as single regioisomers with different pendant linear C2–C20 alkanoyl chains using biocatalytic and chemical acylations. By conventional radical polymerization, these monomers provided high-molecular-weight biobased poly(alkanoyl isosorbide methacrylate)s (PAIMAs). Samples with C2–C12 alkanoyl chains were amorphous with glass transition temperatures from 107 to 54 °C, while C14–C20 chains provided semicrystalline materials with melting points up to 59 °C. Moreover, PAIMAs with C13–C20 chains formed liquid crystalline mesophases with transition temperatures up to 93 °C. The mesophases were studied using polarized optical microscopy, and rheology showed stepwise changes of the viscosity at the transition temperature. Unexpectedly, a PAIMA prepared from a regioisomeric monomer (C18) showed semicrystallinity but not liquid crystallinity. Consequently, the properties of the PAIMAs were readily tunable by controlling the phase structure and transitions through the alkanoyl chain length and the regiochemistry to form fully amorphous, semicrystalline, or semi/liquid crystalline materials.

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          50th Anniversary Perspective: There Is a Great Future in Sustainable Polymers

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            Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review

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              Isosorbide as a Renewable Platform chemical for Versatile Applications-Quo Vadis?

              Isosorbide is a platform chemical of considerable importance for the future replacement of fossil resource-based products. Applications as monomers and building blocks for new polymers and functional materials, new organic solvents, for medical and pharmaceutical applications, and even as fuels or fuel additives are conceivable. The conversion of isosorbide to valuable derivatives by functionalization or substitution of the hydroxyl groups is difficult because of the different configurations of the 2- and 5-positions and the resulting different reactivity and steric hindrance of the two hydroxyl groups. Although a substantial amount of work has been published using exclusively the endo or exo derivatives isomannide and isoidide, respectively, as starting material, a considerable effort is still necessary to transfer and adapt these methods for the efficient conversion of isosorbide. This Minireview deals with all aspects of isosorbide chemistry, which includes its production by catalytic processes, special properties, and chemical transformations for its utilization in biogenic polymers and other applications of interest.
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                Author and article information

                Journal
                Biomacromolecules
                Biomacromolecules
                bm
                bomaf6
                Biomacromolecules
                American Chemical Society
                1525-7797
                1526-4602
                12 December 2020
                08 February 2021
                : 22
                : 2
                : 640-648
                Affiliations
                []Institute of Technology, University of Tartu , Nooruse 1, Tartu 50411, Estonia
                []Department of Chemistry, Lund University , Box 124, Lund 221 00, Sweden
                [§ ]Department of Chemistry and Biotechnology, Tallinn University of Technology , Ehitajate tee 5, Tallinn 19086, Estonia
                Author notes
                Article
                10.1021/acs.biomac.0c01474
                7874169
                33307669
                b03a9333-6b12-4da9-ad36-c4980e6a055b
                © 2020 American Chemical Society

                This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.

                History
                : 13 October 2020
                : 27 November 2020
                Categories
                Article
                Custom metadata
                bm0c01474
                bm0c01474

                Biochemistry
                Biochemistry

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