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Shape-Memory Effect Triggered by π–π Interactions in a Flexible Terpyridine Metal–Organic Framework AITranslate

Adam Mickiewicz University; Adam Mickiewicz University; Northwestern University;Dipartimento di Chimica, Università degli Studi di Torino;Dipartimento di Chimica, Università degli Studi di Torino; University of Maragheh;Chair of Inorganic Chemistry, Technische Universität Dresden;Chair of Inorganic Chemistry, Technische Universität Dresden; University of Stellenbosch; Adam Mickiewicz University;Dipartimento di Chimica, Università degli Studi di Torino
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Publisher: ACS
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Abstract AITranslate

Shape-memory polymers and alloys are adaptable materials capable of reversing from a deformed, metastable phase to an energetically favored original phase in response to external stimuli. In the context of metal–organic frameworks, the term shape-memory is defined as the property of a switchable framework to stabilize the reopened pore phase after the first switching transition. Herein we describe a novel flexible terpyridine MOF which, upon desolvation, transforms into a nonporous structure that reopens into a shape-memory phase when exposed to CO2 at 195 K. Based on comprehensive in situ experimental studies (SC-XRD and PXRD) and DFT energetic considerations combined with literature reports, we recommend dividing shape-memory MOFs into two categories, viz responsive and nonresponsive, depending on the transformability of the gas-free reopened pore phase into the collapsed phase. Furthermore, considering the methodological gap in discovering and understanding shape-memory porous materials, we emphasize the importance of multicycle physisorption experiments for dynamic open framework materials, including metal–organic and covalent organic frameworks.

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DOI:https://doi.org/10.1021/acsmaterialslett.3c00068

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Citation Information:

Shape-memory polymers and alloys are adaptable materials capable of reversing from a deformed, metastable phase to an energetically favored original phase in response to external stimuli. In the context of metal–organic frameworks, the term shape-memory is defined as the property of a switchable framework to stabilize the reopened pore phase after the first switching transition. Herein we describe a novel flexible terpyridine MOF which, upon desolvation, transforms into a nonporous structure that reopens into a shape-memory phase when exposed to CO2 at 195 K. Based on comprehensive in situ experimental studies (SC-XRD and PXRD) and DFT energetic considerations combined with literature reports, we recommend dividing shape-memory MOFs into two categories, viz responsive and nonresponsive, depending on the transformability of the gas-free reopened pore phase into the collapsed phase. Furthermore, considering the methodological gap in discovering and understanding shape-memory porous materials, we emphasize the importance of multicycle physisorption experiments for dynamic open framework materials, including metal–organic and covalent organic frameworks.

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GB/T 7714-2015 [1] Kornel Roztocki, Wiktoria Gromelska, Filip Formalik, et al. ACS Materials Letters, 2023(5). DOI:10.1021/acsmaterialslett.3c00068.
MLA [1] Kornel Roztocki, et al., ACS Materials Letters, no. 5, 2023, https://doi.org/10.1021/acsmaterialslett.3c00068.
APA [1] Kornel Roztocki, Wiktoria Gromelska, Filip Formalik, Alessia Giordana, Luca Andreo, Ghodrat Mahmoudi, Volodymyr Bon, Stefan Kaskel, Leonard J. Barbour, Agnieszka Janiak, & Emanuele Priola. (2023). ACS Materials Letters(5). https://doi.org/10.1021/acsmaterialslett.3c00068
IEEE [1] Kornel Roztocki, Wiktoria Gromelska, Filip Formalik, Alessia Giordana, Luca Andreo, Ghodrat Mahmoudi, Volodymyr Bon, Stefan Kaskel, Leonard J. Barbour, Agnieszka Janiak, and Emanuele Priola, ACS Materials Letters, no. 5, 2023, doi: 10.1021/acsmaterialslett.3c00068.