Preorganization: a powerful tool in intermolecular halogen bonding in solution

  • Preorganization is a powerful tool in supramolecular chemistry which has been utilized successfully in intra‐ and intermolecular halogen bonding. In previous work, we had developed a bidentate bis(iodobenzimidazolium)‐based halogen bond donor which featured a central trifluoromethyl substituent. This compound showed a markedly increased catalytic activity compared to unsubstituted bis(iodoimidazolium)‐based Lewis acids, which could be explained either by electronic effects (the electron withdrawal by the fluorinated substituent) or by preorganization (the hindered rotation of the halogen bonding moieties). Herein, we systematically investigate the origin of this increased Lewis acidity via a comparison of the two types of compounds and their respective derivatives with or without the central trifluoromethyl group. Calorimetric measurements of halide complexations indicated that preorganization is the main reason for the higher halogen bonding strength. The performance of the catalysts in a series of benchmark reactions corroborates this finding.

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Metadaten
Author:Martin VoelkelGND, Patrick WonnerGND, Stefan M. HuberORCiDGND
URN:urn:nbn:de:hbz:294-77949
DOI:https://doi.org/10.1002/open.201900355
Parent Title (English):ChemistryOpen
Subtitle (English):Dedicated to Professor Jean-Marie Lehn on the occasion of his 80th birthday
Publisher:Wiley-VCH Verlag
Place of publication:Weinheim
Document Type:Article
Language:English
Date of Publication (online):2021/01/22
Date of first Publication:2020/02/11
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Tag:Open Access Fonds
Lewis acids; anion recognition; halogen bonding; organocatalysis; solution
Volume:9
First Page:214
Last Page:224
Note:
Article Processing Charge funded by the Deutsche Forschungsgemeinschaft (DFG) and the Open Access Publication Fund of Ruhr-Universität Bochum.
Dewey Decimal Classification:Naturwissenschaften und Mathematik / Chemie, Kristallographie, Mineralogie
open_access (DINI-Set):open_access
faculties:Fakultät für Chemie und Biochemie
Licence (English):License LogoCreative Commons - CC BY-NC-ND 4.0 - Attribution-NonCommercial-NoDerivatives 4.0 International