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Title: Surface‐Enforced Alignment of Reprogrammable Liquid Crystalline Elastomers

Abstract

Abstract Liquid crystalline elastomers (LCEs) are stimuli‐responsive materials capable of undergoing large deformations. The thermomechanical response of LCEs is attributable to the coupling of polymer network properties and disruption of order between liquid crystalline mesogens. Complex deformations have been realized in LCEs by either programming the nematic director via surface‐enforced alignment or localized mechanical deformation in materials incorporating dynamic covalent chemistries. Here, the preparation of LCEs via thiol‐Michael addition reaction is reported that are amenable to surface‐enforced alignment. Afforded by the thiol‐Michael addition reaction, dynamic covalent bonds are uniquely incorporated in chemistries subject to surface‐enforce alignment. Accordingly, LCEs prepared with complex director profiles are able to be programmed and reprogrammed by (re)activating the dynamic covalent chemistry to realize distinctive shape transformations.

Authors:
 [1];  [2];  [3];  [3]; ORCiD logo [3]
  1. Department of Chemical and Biological Engineering University of Colorado Boulder CO 80303 USA
  2. Department of Chemical and Biological Engineering University of Colorado Boulder CO 80303 USA, Medical Scientist Training Program University of Colorado Anschutz Medical Campus Aurora CO 80045 USA
  3. Department of Chemical and Biological Engineering University of Colorado Boulder CO 80303 USA, Materials Science and Engineering Program University of Colorado Boulder CO 80303 USA
Publication Date:
Sponsoring Org.:
USDOE
OSTI Identifier:
1882791
Alternate Identifier(s):
OSTI ID: 1882792
Resource Type:
Published Article
Journal Name:
Advanced Science
Additional Journal Information:
Journal Name: Advanced Science Journal Volume: 9 Journal Issue: 29; Journal ID: ISSN 2198-3844
Publisher:
Wiley Blackwell (John Wiley & Sons)
Country of Publication:
Germany
Language:
English

Citation Formats

Hebner, Tayler S., Kirkpatrick, Bruce E., Anseth, Kristi S., Bowman, Christopher N., and White, Timothy J. Surface‐Enforced Alignment of Reprogrammable Liquid Crystalline Elastomers. Germany: N. p., 2022. Web. doi:10.1002/advs.202204003.
Hebner, Tayler S., Kirkpatrick, Bruce E., Anseth, Kristi S., Bowman, Christopher N., & White, Timothy J. Surface‐Enforced Alignment of Reprogrammable Liquid Crystalline Elastomers. Germany. https://doi.org/10.1002/advs.202204003
Hebner, Tayler S., Kirkpatrick, Bruce E., Anseth, Kristi S., Bowman, Christopher N., and White, Timothy J. Sun . "Surface‐Enforced Alignment of Reprogrammable Liquid Crystalline Elastomers". Germany. https://doi.org/10.1002/advs.202204003.
@article{osti_1882791,
title = {Surface‐Enforced Alignment of Reprogrammable Liquid Crystalline Elastomers},
author = {Hebner, Tayler S. and Kirkpatrick, Bruce E. and Anseth, Kristi S. and Bowman, Christopher N. and White, Timothy J.},
abstractNote = {Abstract Liquid crystalline elastomers (LCEs) are stimuli‐responsive materials capable of undergoing large deformations. The thermomechanical response of LCEs is attributable to the coupling of polymer network properties and disruption of order between liquid crystalline mesogens. Complex deformations have been realized in LCEs by either programming the nematic director via surface‐enforced alignment or localized mechanical deformation in materials incorporating dynamic covalent chemistries. Here, the preparation of LCEs via thiol‐Michael addition reaction is reported that are amenable to surface‐enforced alignment. Afforded by the thiol‐Michael addition reaction, dynamic covalent bonds are uniquely incorporated in chemistries subject to surface‐enforce alignment. Accordingly, LCEs prepared with complex director profiles are able to be programmed and reprogrammed by (re)activating the dynamic covalent chemistry to realize distinctive shape transformations.},
doi = {10.1002/advs.202204003},
journal = {Advanced Science},
number = 29,
volume = 9,
place = {Germany},
year = {Sun Aug 21 00:00:00 EDT 2022},
month = {Sun Aug 21 00:00:00 EDT 2022}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record
https://doi.org/10.1002/advs.202204003

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