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Stereocomplexes of Discrete, Isotactic Lactic Acid Oligomers Conjugated with Oligodimethylsiloxanes

[Image: see text] Discrete length block co-oligomers (BCOs) comprised of a crystalline and an amorphous block are a new class of materials that gives highly ordered lamellar morphologies at small length scales. Here, we show the preparation of discrete, isotactic oligo l- and d-lactic acid (olLA and...

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Autores principales: Lamers, Brigitte A. G., van Genabeek, Bas, Hennissen, J., de Waal, Bas F. M., Palmans, Anja R. A., Meijer, E. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376449/
https://www.ncbi.nlm.nih.gov/pubmed/30792554
http://dx.doi.org/10.1021/acs.macromol.8b02529
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author Lamers, Brigitte A. G.
van Genabeek, Bas
Hennissen, J.
de Waal, Bas F. M.
Palmans, Anja R. A.
Meijer, E. W.
author_facet Lamers, Brigitte A. G.
van Genabeek, Bas
Hennissen, J.
de Waal, Bas F. M.
Palmans, Anja R. A.
Meijer, E. W.
author_sort Lamers, Brigitte A. G.
collection PubMed
description [Image: see text] Discrete length block co-oligomers (BCOs) comprised of a crystalline and an amorphous block are a new class of materials that gives highly ordered lamellar morphologies at small length scales. Here, we show the preparation of discrete, isotactic oligo l- and d-lactic acid (olLA and odLA) homoblocks followed by ligation to oligodimethylsiloxane (oDMS), affording a library of crystalline–amorphous BCOs that vary in molecular weight and composition. Mixing the two enantiomeric BCOs or homoblocks results in the formation of the corresponding stereocomplex. The properties and phase behavior of the isotactic (block co)oligomers and the stereocomplexes thereof are studied using differential scanning calorimetry and small-angle X-ray scattering. A systematic study of the isotactic homoblock lengths and crystal structure confirmed the formation of a 10(3) helix with a monomeric rise of 0.3 nm, whereas the stereocomplex adopts a 3(1) helix. The same type of crystal structure was found for the isotactic and stereocomplex of BCOs giving rise to the formation of lamellar morphologies at room temperature as a result of crystallization of the oLA blocks. Distorted lamellar structures were found in BCOs that preorganize into nonlamellar morphologies prior to crystallization. The stereocomplex BCOs shows more crystal defects and a loss of long-range ordering in the microstructure due to the larger driving force for crystallization. Hence, the balance between chain length, block volume, and the crystallization strength are of major importance for the formation of the final structure with the least defects.
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spelling pubmed-63764492019-02-19 Stereocomplexes of Discrete, Isotactic Lactic Acid Oligomers Conjugated with Oligodimethylsiloxanes Lamers, Brigitte A. G. van Genabeek, Bas Hennissen, J. de Waal, Bas F. M. Palmans, Anja R. A. Meijer, E. W. Macromolecules [Image: see text] Discrete length block co-oligomers (BCOs) comprised of a crystalline and an amorphous block are a new class of materials that gives highly ordered lamellar morphologies at small length scales. Here, we show the preparation of discrete, isotactic oligo l- and d-lactic acid (olLA and odLA) homoblocks followed by ligation to oligodimethylsiloxane (oDMS), affording a library of crystalline–amorphous BCOs that vary in molecular weight and composition. Mixing the two enantiomeric BCOs or homoblocks results in the formation of the corresponding stereocomplex. The properties and phase behavior of the isotactic (block co)oligomers and the stereocomplexes thereof are studied using differential scanning calorimetry and small-angle X-ray scattering. A systematic study of the isotactic homoblock lengths and crystal structure confirmed the formation of a 10(3) helix with a monomeric rise of 0.3 nm, whereas the stereocomplex adopts a 3(1) helix. The same type of crystal structure was found for the isotactic and stereocomplex of BCOs giving rise to the formation of lamellar morphologies at room temperature as a result of crystallization of the oLA blocks. Distorted lamellar structures were found in BCOs that preorganize into nonlamellar morphologies prior to crystallization. The stereocomplex BCOs shows more crystal defects and a loss of long-range ordering in the microstructure due to the larger driving force for crystallization. Hence, the balance between chain length, block volume, and the crystallization strength are of major importance for the formation of the final structure with the least defects. American Chemical Society 2019-01-29 2019-02-12 /pmc/articles/PMC6376449/ /pubmed/30792554 http://dx.doi.org/10.1021/acs.macromol.8b02529 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Lamers, Brigitte A. G.
van Genabeek, Bas
Hennissen, J.
de Waal, Bas F. M.
Palmans, Anja R. A.
Meijer, E. W.
Stereocomplexes of Discrete, Isotactic Lactic Acid Oligomers Conjugated with Oligodimethylsiloxanes
title Stereocomplexes of Discrete, Isotactic Lactic Acid Oligomers Conjugated with Oligodimethylsiloxanes
title_full Stereocomplexes of Discrete, Isotactic Lactic Acid Oligomers Conjugated with Oligodimethylsiloxanes
title_fullStr Stereocomplexes of Discrete, Isotactic Lactic Acid Oligomers Conjugated with Oligodimethylsiloxanes
title_full_unstemmed Stereocomplexes of Discrete, Isotactic Lactic Acid Oligomers Conjugated with Oligodimethylsiloxanes
title_short Stereocomplexes of Discrete, Isotactic Lactic Acid Oligomers Conjugated with Oligodimethylsiloxanes
title_sort stereocomplexes of discrete, isotactic lactic acid oligomers conjugated with oligodimethylsiloxanes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376449/
https://www.ncbi.nlm.nih.gov/pubmed/30792554
http://dx.doi.org/10.1021/acs.macromol.8b02529
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