The role of halogen bonds in the catalytic mechanism of the iso-Nazarov cyclization reaction: a DFT study?
Physical Chemistry Chemical Physics Pub Date: 2022-07-20 DOI: 10.1039/D2CP01913B
Abstract
With the continuous development of halogen bonds, halogen bond donors have been used as clean and efficient catalysts in organic reactions. In this work, with inorganic halides (I2, IBr, ICl, and ICl3) as catalysts and the iso-Nazarov cyclization as the benchmark reaction, we aim at investigating the role of the halogen bond in the catalytic mechanism. The halogen bond catalyzed iso-Nazarov cyclization reaction involves three steps: carbon–carbon coupling process, [1,2]-H shift process, and [1,4]-H shift process. The halogen-bonding interaction promotes the charge accumulation of the oxygen atom in the carbonyl group and decreases the activation energy of the reaction. The catalytic activity of the halogen bond donor is enhanced in the order of I2 < IBr < ICl < ICl3, and it could be predicted that the partial covalent interaction of the I?O halogen bond between the catalyst ICl3 and the oxygen atom of the reactant may exhibit good catalytic activity in the experiments. In the [1,4]-H shift process, the two-step hydrogen bond/halogen bond co-catalyzed mechanism exhibits the lowest reaction energy barrier than the one-step water co-catalyzed proton transfer mechanism and the direct one.
Recommended Literature
- [1] Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials? Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-GarayoaRSC Adv., 2017,7, 24133-24139 10.1039/C7RA03845C
- [2] Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue GaoRSC Adv., 2017,7, 34392-34400 10.1039/C7RA05271E
- [3] Emergence of cationic polyamine dendrimersomes: design, stimuli sensitivity and potential biomedical applications Partha Laskar,Christine DufèsNanoscale Adv., 2021,3, 6007-6026 10.1039/D1NA00536G
- [4] Evidence of pre-micellar aggregates in aqueous solution of amphiphilic PDMS–PEO block copolymer? Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa CaccamoPhys. Chem. Chem. Phys., 2019,21, 11983-11991 10.1039/C9CP02195G
- [5] Essential effect of the electrolyte on the mechanical and chemical degradation of LiNi0.8Co0.15Al0.05O2 cathodes upon long-term cycling?? Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang ChiJ. Mater. Chem. A, 2021,9, 2111-2119 10.1039/D0TA07814J
- [6] Evolution and characterization of a benzylguanine-binding RNA aptamer? J. Xu,T. J. Carrocci,A. A. HoskinsChem. Commun., 2016,52, 549-552 10.1039/C5CC07605F
- [7] Dissociation of aryl sulfonyl phthalimide radical anions: relevance to the biological activity of arylsulfonyl amides? Abdelaziz Houmam,Emad M. HamedChem. Commun., 2012,48, 11328-11330 10.1039/C2CC36835H
- [8] Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-MoralesCrystEngComm, 2013,15, 2206-2212 10.1039/C2CE26556G
- [9] Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe? Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. MarqueChem. Sci., 2021,12, 4154-4161 10.1039/D0SC06470J
- [10] Fast synthesis of copper nanoclusters through the use of hydrogen peroxide additive and their application for the fluorescence detection of Hg2+ in water samples? Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu JunkangNew J. Chem., 2015,39, 5240-5248 10.1039/C5NJ00831J
Journal Name:Physical Chemistry Chemical Physics
research_products
-
CAS no.: 89640-58-4