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Elisabeth M. Fatila

Researcher at Indiana University

Publications -  25
Citations -  716

Elisabeth M. Fatila is an academic researcher from Indiana University. The author has contributed to research in topics: Coordination complex & Ligand. The author has an hindex of 14, co-authored 24 publications receiving 601 citations. Previous affiliations of Elisabeth M. Fatila include Louisiana Tech University & University of Guelph.

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Fine-tuning the single-molecule magnet properties of a [Dy(III)-radical]2 pair.

TL;DR: These unique results illustrate how the dynamics of a supramolecular [Dy-Radical]2 SMM can be fine-tuned by the exchange-bias and an applied magnetic field.
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Anions Stabilize Each Other inside Macrocyclic Hosts

TL;DR: It is shown that two bisulfate anions can form such dimers, which stabilize each other with self-complementary hydrogen bonds, by encapsulation inside a pair of cyanostar macrocycles.
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Phosphate–phosphate oligomerization drives higher order co-assemblies with stacks of cyanostar macrocycles

TL;DR: In this paper, a tetrameric stack of planar cyanostar macrocycles threaded by a phosphate trimer is shown to form a tubular, highly electropositive cavity that complements the size and shape of the phosphate oligomers.
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Ion Pairing and Co-facial Stacking Drive High-Fidelity Bisulfate Assembly with Cyanostar Macrocyclic Hosts.

TL;DR: Thermodynamic stabilization of hydroxyanion dimers demonstrates the ability to use macrocycles to control ion speciation and stoichiometry of the overall assemblies and sees unprecedented evidence for a water molecule bound to the complex in the acetonitrile solution.
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Extreme Stabilization and Redox Switching of Organic Anions and Radical Anions by Large-Cavity, CH Hydrogen-Bonding Cyanostar Macrocycles

TL;DR: This work demonstrates the encapsulation and noncovalent stabilization of organic radical anions by C-H hydrogen bonding in π-stacked pairs of cyanostar macrocycles having large cavities and opens up a new approach to capturing and studying unstable anions and aradical anions when encapsulated by size-complementary anion receptors.