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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/50544
Title: Halogen bonds in N-bromosuccinimide and other N-halosuccinimides
Authors: Pakorn Bovonsombat
Samantha Stone
Miriam Rossi
Francesco Caruso
Vassar College
Mahidol University
Keywords: Chemistry
Issue Date: 1-Dec-2019
Citation: Structural Chemistry. Vol.30, No.6 (2019), 2205-2215
Abstract: © 2019, Springer Science+Business Media, LLC, part of Springer Nature. Our crystal data shows marked intermolecular Br interaction with a neighboring O (carbonyl) in the crystal, Br---O(carbonyl) = 2.767(1) Å, well below the sum of the corresponding van der Waals radii, 3.37 Å. This C=O---Br interaction is among the shortest in the CSD (only 8/2185 examples have a similar distance 2.725–2.800 Å). Only one carbonyl group interacts with the halogen atom, thus inducing a helical intermolecular arrangement. The halogen bond was also studied with density functional theory (DFT) methods, based on coordinates of two molecules in the crystal packing, widely modifying the N-Br---O(carbonyl) angle. In each calculation, this angle was fixed, and the corresponding arrangements were analyzed for potential structural correlation. Indeed, the widening of the N-Br---O(carbonyl) angle correlates with a gradual increase of halogen bond interaction Br---O(carbonyl), that is, shorter separation. It is also seen that decreasing the N-Br---O(carbonyl) angle is associated with decreasing Br---Br separation. Isosurface electron density shows the presence of Br sigma-holes in the two-molecule arrangements.
URI: http://repository.li.mahidol.ac.th/dspace/handle/123456789/50544
metadata.dc.identifier.url: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85065530212&origin=inward
ISSN: 15729001
10400400
Appears in Collections:Scopus 2019

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