A Quantum‐chemical Analysis on the Lewis Acidity of Diarylhalonium Ions-Reference-Cited by-同舟云学术

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A Quantum‐chemical Analysis on the Lewis Acidity of Diarylhalonium Ions

Published:2022-10-05 Issue:1 Volume:24 Page:
ISSN:1439-4235
Container-title:ChemPhysChem
language:en
Short-container-title:ChemPhysChem

Author:

Robidas Raphaël¹^ORCID,Reinhard Dominik L.²,Huber Stefan M.²^ORCID,Legault Claude Y.¹^ORCID

Affiliation:

1. Department of Chemistry Université de Sherbrooke Centre in Green Chemistry and Catalysis J1K 2R1 Sherbrooke Québec Canada

2. Fakultät für Chemie und Biochemie Organische Chemie I Ruhr-Universität Bochum Universitätsstraße 150 44801 Bochum Germany

Funder

Canada Foundation for Innovation

Fonds de recherche du Québec – Nature et technologies

Natural Sciences and Engineering Research Council of Canada

Deutsche Forschungsgemeinschaft

Fonds der Chemischen Industrie

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,Atomic and Molecular Physics, and Optics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cphc.202200634

Reference32 articles.

1. Supramolecular Catalysis

2. Asymmetric Catalysis by Chiral Hydrogen-Bond Donors

3. Asymmetrische Katalyse durch chirale Wasserstoffbrückendonoren

4. (Thio)urea organocatalysis—What can be learnt from anion recognition?

5. The Emergence of Anion−π Catalysis

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1. Recent Progress in Synthetic Applications of Hypervalent Iodine(III) Reagents;Chemical Reviews;2024-09-13

2. Halogen, Chalcogen, Pnictogen, and Tetrel Bonding in Non‐Covalent Organocatalysis: An Update;Angewandte Chemie International Edition;2024-07-02

3. Nichtkovalente Organokatalyse mit Halogen‐, Chalkogen‐, Pniktogen‐ und Tetrelbrücken: neuere Entwicklungen;Angewandte Chemie;2024-07-02

4. A comparison of structure, bonding and non-covalent interactions of aryl halide and diarylhalonium halogen-bond donors;Beilstein Journal of Organic Chemistry;2024-06-27

5. Evaluation of a Bidentate ‘Clamp-Like’ Halogen-Bond Donor Motif Based on Iodonium(III) Moieties;Synlett;2023-10-25

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