Dynamic reaction-induced phase separation in tunable, adaptive covalent networks [electronic resource]

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Bibliographic Details
Online Access: Full Text (via OSTI)
Corporate Author: Argonne National Laboratory (Researcher)
Format: Government Document Electronic eBook
Language:English
Published: Argonne, Ill. : Oak Ridge, Tenn. : Argonne National Laboratory ; Distributed by the Office of Scientific and Technical Information, U.S. Department of Energy, 2020.
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MARC

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245 0 0 |a Dynamic reaction-induced phase separation in tunable, adaptive covalent networks  |h [electronic resource] 
260 |a Argonne, Ill. :  |b Argonne National Laboratory ;  |a Oak Ridge, Tenn. :  |b Distributed by the Office of Scientific and Technical Information, U.S. Department of Energy,  |c 2020. 
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500 |a "Journal ID: ISSN 2041-6520." 
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500 |a ": US2208822." 
500 |a Herbert, Katie M. ; Getty, Patrick T. ; Dolinski, Neil D. ; Hertzog, Jerald E. ; de Jong, Derek ; Lettow, James H. ; Romulus, Joy ; Onorato, Jonathan W. ; Foster, Elizabeth M. ; Rowan, Stuart J. ; et al. 
500 |a USDOE. 
500 |a National Institute of Standards and Technology (NIST) 
520 3 |a A series of catalyst-free, room temperature dynamic bonds derived from a reversible thia-Michael reaction are utilized to access mechanically robust dynamic covalent network films. The equilibrium of the thiol addition to benzalcyanoacetate-based Michael-acceptors can be directly tuned by controlling the electron-donating/withdrawing nature of the Michael-acceptor. By modulating the composition of different Michael-acceptors in a dynamic covalent network, a wide range of mechanical properties and thermal responses can be realized. Additionally, the reported systems phase-separate in a process, coined dynamic reaction-induced phase separation (DRIPS), that yields reconfigurable phase morphologies and reprogrammable shape-memory behaviour as highlighted by the heat-induced folding of a predetermined structure. 
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650 7 |a 37 inorganic, organic, physical, and analytical chemistry  |2 local. 
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