The “nitrogen effect” : Complexation with macrocycles potentiates fused heterocycles to form halogen bonds in competitive solvents
Twum, K., Nadimi, S., Osei, F. B., Puttreddy, R., Ojong, Y. B., Hayward, J. J., Rissanen, K., Trant, J. F., & Beyeh, N. K. (2023). The “nitrogen effect” : Complexation with macrocycles potentiates fused heterocycles to form halogen bonds in competitive solvents. Chemistry : An Asian Journal, Early online. https://doi.org/10.1002/asia.202201308
Published in
Chemistry : An Asian JournalAuthors
Date
2023Access restrictions
Embargoed until: 2024-01-27Request copy from author
Copyright
© 2023 Wiley-VCH GmbH
Weak intermolecular forces are typically very difficult to observe in highly competitive polar protic solvents as they are overwhelmed by the quantity of competing solvent. This is even more challenging for three-component ternary assemblies of pure organic compounds. In this work, we overcome these complications by leveraging the binding of fused aromatic N-heterocycles in an open resorcinarene cavity to template the formation of a three-component halogen-bonded ternary assembly in a protic polar solvent system.
Publisher
Wiley-VCH VerlagISSN Search the Publication Forum
1861-4728Keywords
Publication in research information system
https://converis.jyu.fi/converis/portal/detail/Publication/176548163
Metadata
Show full item recordCollections
Related funder(s)
Academy of FinlandFunding program(s)
Academy Project, AoF
Additional information about funding
We gratefully acknowledge financial support from the American Chemical Society (NKB: ACS-PRF grant no. 39427), Oakland University, MI, the Academy of Finland (KR: grant no. 317259), and the University of Jyväskylä. We also acknowledge the financial support from the Natural Sciences and Engineering Research Council of Canada (JFT: grant no. 2018-06338) and the Ontario Early Researcher Award (JFT: grant no. ER18-14-114)

License
Related items
Showing items with similar title or keywords.
-
Design and construction of halogen-bonded capsules and cages
Turunen, Lotta (University of Jyväskylä, 2017)This thesis describes the design, synthesis and characterization of supramolecular halogen-bonded capsules and cages from multivalent ligands. In the first part of the thesis, an overview to halogen bonding is provided. ... -
Solid state halogen bonded networks vs. dynamic assemblies in solution: explaining N⋯X interactions of multivalent building blocks
Tero, Tiia-Riikka; Salorinne, Kirsi; Malola, Sami; Häkkinen, Hannu; Nissinen, Maija (Royal Society of Chemistry, 2015)Tetrapyridine functionalized resorcinarene macrocycles were used as multivalent building blocks for the construction of halogen bonded networks with aryl halide linkers. In the solid state, resorcinarene macrocycles and ... -
N-Heterocyclic Carbene Catalyzed Quadruple Domino Reactions through α,β-Unsaturated Acyl Azolium Intermediates : Asymmetric Synthesis of Cyclopenta[c]chromenones
Liu, Qiang; Chen, Xiang-Yu; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter (Wiley, VCH Verlag GmbH & Co. KGaA, 2018)An N‐heterocyclic carbene catalyzed domino sequence via α,β‐unsaturated acyl azolium intermediates has been developed. This strategy provides a convenient enantioselective route to functionalized tricyclic coumarin derivatives ... -
N-Heterocyclic Carbene Catalyzed Asymmetric Synthesis of Pentacyclic Spirooxindoles via [3+3] Annulations of Isatin-Derived Enals and Cyclic N-Sulfonyl Ketimines
Liu, Qiang; Chen, Xiangyu; Li, Sun; Rissanen, Kari; Enders, Dieter (Wiley - VCH Verlag GmbH & Co. KGaA, 2019)A convenient enantioselective route to new types of pentacyclic spirooxindoles via [3+3] annulation reactions of isatin-derived enals and cyclic N-sulfonyl ketimines, using N-heterocyclic carbene (NHC) catalysis has ... -
Highly Enantioselective Kinetic Resolution of Michael Adducts through N-Heterocyclic Carbene Catalysis : An Efficient Asymmetric Route to Cyclohexenes
Chen, Xiang-Yu; Li, Sun; Liu, Qiang; Kumar, Mukesh; Peuronen, Anssi; Rissanen, Kari; Enders, Dieter (Wiley, 2018)Ahighly efficient strategy for the kinetic resolu-tion of Michael adductswas realized using achiral N-het-erocyclic carbene catalyst.The kinetic resolution providesanew convenientroute to single diastereomers of cyclo-hexenes ...