Rational design and topochemical synthesis of polymorphs of a polymer

Packing a polymer in different ways can give polymorphs of the polymer having different properties. β-Turn forming peptides such as 2-aminoisobutyric acid (Aib)-rich peptides adopt several conformations by varying the dihedral angles. Aiming at this, a β-turn-forming peptide monomer would give diffe...

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Main Authors: Athiyarath, Vignesh, Mathew, Liby Ann, Zhao, Yakai, Khazeber, Ravichandran, Ramamurty, Upadrasta, Sureshan, Kana M.
Other Authors: School of Mechanical and Aerospace Engineering
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/169779
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1697792023-08-05T16:48:34Z Rational design and topochemical synthesis of polymorphs of a polymer Athiyarath, Vignesh Mathew, Liby Ann Zhao, Yakai Khazeber, Ravichandran Ramamurty, Upadrasta Sureshan, Kana M. School of Mechanical and Aerospace Engineering Engineering::Mechanical engineering Science::Chemistry Aminoisobutyric Acid Acid-Rich Peptides Packing a polymer in different ways can give polymorphs of the polymer having different properties. β-Turn forming peptides such as 2-aminoisobutyric acid (Aib)-rich peptides adopt several conformations by varying the dihedral angles. Aiming at this, a β-turn-forming peptide monomer would give different polymorphs and these polymorphs upon topochemical polymerization would yield polymorphs of the polymer, we designed an Aib-rich monomer N3-(Aib)3-NHCH2-C[triple bond, length as m-dash]CH. This monomer crystallizes as two polymorphs and one hydrate. In all forms, the peptide adopts β-turn conformations and arranges in a head-to-tail manner with their azide and alkyne units proximally placed in a ready-to-react alignment. On heating, both the polymorphs undergo topochemical azide-alkyne cycloaddition polymerization. Polymorph I polymerized in a single-crystal-to-single-crystal (SCSC) fashion and the single-crystal X-ray diffraction analysis of the polymer revealed its screw-sense reversing helical structure. Polymorph II maintains its crystallinity during polymerization but gradually becomes amorphous upon storage. The hydrate III undergoes a dehydrative transition to polymorph II. Nanoindentation studies revealed that different polymorphs of the monomer and the corresponding polymers exhibited different mechanical properties, in accordance with their crystal packing. This work demonstrates the promising future of the marriage of polymorphism and topochemistry for obtaining polymorphs of polymers. Published version K. M. S. thanks the Department of Science and Technology, Ministry of Science and Technology, Government of India, for a Swarna-Jayanti fellowship (DST/SJF/CSA02/2012-13), and the Science and Engineering Research Board, India, for the research grant (SERB/CRG/000577/2018). All publication charges for this article have been paid for by the Royal Society of Chemistry. 2023-08-02T06:59:59Z 2023-08-02T06:59:59Z 2023 Journal Article Athiyarath, V., Mathew, L. A., Zhao, Y., Khazeber, R., Ramamurty, U. & Sureshan, K. M. (2023). Rational design and topochemical synthesis of polymorphs of a polymer. Chemical Science, 14(19), 5132-5140. https://dx.doi.org/10.1039/d3sc00053b 2041-6520 https://hdl.handle.net/10356/169779 10.1039/d3sc00053b 37206383 2-s2.0-85153947645 19 14 5132 5140 en Chemical Science © 2023 The Author(s). Published by the Royal Society of Chemistry. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Mechanical engineering
Science::Chemistry
Aminoisobutyric Acid
Acid-Rich Peptides
spellingShingle Engineering::Mechanical engineering
Science::Chemistry
Aminoisobutyric Acid
Acid-Rich Peptides
Athiyarath, Vignesh
Mathew, Liby Ann
Zhao, Yakai
Khazeber, Ravichandran
Ramamurty, Upadrasta
Sureshan, Kana M.
Rational design and topochemical synthesis of polymorphs of a polymer
description Packing a polymer in different ways can give polymorphs of the polymer having different properties. β-Turn forming peptides such as 2-aminoisobutyric acid (Aib)-rich peptides adopt several conformations by varying the dihedral angles. Aiming at this, a β-turn-forming peptide monomer would give different polymorphs and these polymorphs upon topochemical polymerization would yield polymorphs of the polymer, we designed an Aib-rich monomer N3-(Aib)3-NHCH2-C[triple bond, length as m-dash]CH. This monomer crystallizes as two polymorphs and one hydrate. In all forms, the peptide adopts β-turn conformations and arranges in a head-to-tail manner with their azide and alkyne units proximally placed in a ready-to-react alignment. On heating, both the polymorphs undergo topochemical azide-alkyne cycloaddition polymerization. Polymorph I polymerized in a single-crystal-to-single-crystal (SCSC) fashion and the single-crystal X-ray diffraction analysis of the polymer revealed its screw-sense reversing helical structure. Polymorph II maintains its crystallinity during polymerization but gradually becomes amorphous upon storage. The hydrate III undergoes a dehydrative transition to polymorph II. Nanoindentation studies revealed that different polymorphs of the monomer and the corresponding polymers exhibited different mechanical properties, in accordance with their crystal packing. This work demonstrates the promising future of the marriage of polymorphism and topochemistry for obtaining polymorphs of polymers.
author2 School of Mechanical and Aerospace Engineering
author_facet School of Mechanical and Aerospace Engineering
Athiyarath, Vignesh
Mathew, Liby Ann
Zhao, Yakai
Khazeber, Ravichandran
Ramamurty, Upadrasta
Sureshan, Kana M.
format Article
author Athiyarath, Vignesh
Mathew, Liby Ann
Zhao, Yakai
Khazeber, Ravichandran
Ramamurty, Upadrasta
Sureshan, Kana M.
author_sort Athiyarath, Vignesh
title Rational design and topochemical synthesis of polymorphs of a polymer
title_short Rational design and topochemical synthesis of polymorphs of a polymer
title_full Rational design and topochemical synthesis of polymorphs of a polymer
title_fullStr Rational design and topochemical synthesis of polymorphs of a polymer
title_full_unstemmed Rational design and topochemical synthesis of polymorphs of a polymer
title_sort rational design and topochemical synthesis of polymorphs of a polymer
publishDate 2023
url https://hdl.handle.net/10356/169779
_version_ 1773551349378580480