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Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability

Controlling thermal expansion (TE) behaviors of organic materials is challenging because several mechanisms can govern TE, such as noncovalent interaction strength and structural motions. Here, we report the first demonstration of tuning TE within organic solids by using a mixed cocrystal approach....

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Autores principales: Ding, Xiaodan, Unruh, Daniel K., Groeneman, Ryan H., Hutchins, Kristin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480503/
https://www.ncbi.nlm.nih.gov/pubmed/32953037
http://dx.doi.org/10.1039/d0sc02795b
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author Ding, Xiaodan
Unruh, Daniel K.
Groeneman, Ryan H.
Hutchins, Kristin M.
author_facet Ding, Xiaodan
Unruh, Daniel K.
Groeneman, Ryan H.
Hutchins, Kristin M.
author_sort Ding, Xiaodan
collection PubMed
description Controlling thermal expansion (TE) behaviors of organic materials is challenging because several mechanisms can govern TE, such as noncovalent interaction strength and structural motions. Here, we report the first demonstration of tuning TE within organic solids by using a mixed cocrystal approach. The mixed cocrystals contain three unique molecules, two of which are present in variable ratios. These two molecules either lack or exhibit the ability to undergo molecular motion in the solid state. Incorporation of higher ratios of motion-capable molecules results in larger, positive TE along the motion direction. Addition of a motion-incapable molecule affords solids that undergo less TE. Fine-tuned TE behavior was attained by systematically controlling the ratio of motion-capable and -incapable molecules in each solid.
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spelling pubmed-74805032020-09-18 Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability Ding, Xiaodan Unruh, Daniel K. Groeneman, Ryan H. Hutchins, Kristin M. Chem Sci Chemistry Controlling thermal expansion (TE) behaviors of organic materials is challenging because several mechanisms can govern TE, such as noncovalent interaction strength and structural motions. Here, we report the first demonstration of tuning TE within organic solids by using a mixed cocrystal approach. The mixed cocrystals contain three unique molecules, two of which are present in variable ratios. These two molecules either lack or exhibit the ability to undergo molecular motion in the solid state. Incorporation of higher ratios of motion-capable molecules results in larger, positive TE along the motion direction. Addition of a motion-incapable molecule affords solids that undergo less TE. Fine-tuned TE behavior was attained by systematically controlling the ratio of motion-capable and -incapable molecules in each solid. Royal Society of Chemistry 2020-06-05 /pmc/articles/PMC7480503/ /pubmed/32953037 http://dx.doi.org/10.1039/d0sc02795b Text en This journal is © The Royal Society of Chemistry 2020 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Ding, Xiaodan
Unruh, Daniel K.
Groeneman, Ryan H.
Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
title Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
title_full Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
title_fullStr Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
title_full_unstemmed Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
title_short Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
title_sort controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480503/
https://www.ncbi.nlm.nih.gov/pubmed/32953037
http://dx.doi.org/10.1039/d0sc02795b
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