TY - JOUR
T1 - Crystallization of Small Organic Molecules in a Polymer Matrix
T2 - Multistep Mechanism Enables Structural Control
AU - Bronshtein, Ily A.
AU - Weissman, Haim
AU - Kaplan-Ashiri, Ifat
AU - Rybtchinski, Boris
N1 - This work was supported by grants from the Israel Science Foundation, Minerva Foundation, and the Helen and Martin Kimmel Center for Molecular Design. The authors thank S. Semenov for help with numerical simulations of the crystallization kinetics.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - The widely employed crystallization of organic molecules in solution is not well understood and is difficult to control. Employing polymers as crystallization media may allow enhanced control via temperature-induced regulation of polymer dynamics. Crystallization of a small organic molecule (perylene diimide) is investigated in polymer matrices (polystyrene) that enable the mechanistic study and control over order evolution. The crystallization is induced by heating above the glass transition temperature of the polymer, and quenched by cooling, leading to stabilization of crystallization intermediates. The mechanistic studies include direct imaging by electron microscopy, revealing a complex self-assembly process starting from amorphous aggregates that densify and transform into an unstable crystalline phase of N,N '-bis(2,6-dimethylphenyl)perylene-3,4,9,10-tetracarboxylic diimide (DMP-PDI), followed by a conversion into a more stable crystalline form. Stabilization of crystallization intermediates at room temperature provides diverse structures based on a single molecular component. These findings have implications for the rational design of organic crystalline materials.
AB - The widely employed crystallization of organic molecules in solution is not well understood and is difficult to control. Employing polymers as crystallization media may allow enhanced control via temperature-induced regulation of polymer dynamics. Crystallization of a small organic molecule (perylene diimide) is investigated in polymer matrices (polystyrene) that enable the mechanistic study and control over order evolution. The crystallization is induced by heating above the glass transition temperature of the polymer, and quenched by cooling, leading to stabilization of crystallization intermediates. The mechanistic studies include direct imaging by electron microscopy, revealing a complex self-assembly process starting from amorphous aggregates that densify and transform into an unstable crystalline phase of N,N '-bis(2,6-dimethylphenyl)perylene-3,4,9,10-tetracarboxylic diimide (DMP-PDI), followed by a conversion into a more stable crystalline form. Stabilization of crystallization intermediates at room temperature provides diverse structures based on a single molecular component. These findings have implications for the rational design of organic crystalline materials.
UR - http://www.scopus.com/inward/record.url?scp=85070186591&partnerID=8YFLogxK
U2 - 10.1002/smll.201902936
DO - 10.1002/smll.201902936
M3 - مقالة
SN - 1613-6810
VL - 15
JO - Small
JF - Small
IS - 38
M1 - 1902936
ER -