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Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Chemical Oxidation of Chrysene: A Structural and Theoretical Description of a Mixed-Valent Trimeric Radical Cation
Megan E McCormack1, Rameswar Bhattacharjee2, Zheng Wei1
1Department of Chemistry, University at Albany, State University of New York, Albany, New York 12222, United States.
Abstract:
Chemical oxidation of chrysene with GaCl3 affords a trimeric chrysene radical dication, [(C18H12)3]2+, crystallized with two Ga2Cl7 - anions, as revealed by single crystal X-ray diffraction analysis. In the crystal structure, 1D π-stacked columns of chrysene with interplanar contacts averaged at 3.303(3) Å are separated by Ga2Cl7 - anions. Computational studies reveal that the positive charge is concentrated largely on the terminal chrysene units with charges of +0.84 and +0.80, while the center chrysene has a comparatively lower charge of +0.36. This charge distribution is corroborated with structural features of the trimer, as the terminal chrysene molecules exhibit a more pronounced core deformation. Taking the neutral trimer as a reference, much weaker interactions are observed in the title chrysene trimer bearing a +2 charge, suggesting the presence of substantial electrostatic repulsion.
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