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Intramolecular pi-pi stacking interactions in 2-substituted N,N-dibenzylaziridinium ions and their regioselectivity in nucleophilic ring-opening reactions

Saron Catak UGent, Matthias D'hooghe UGent, Norbert De Kimpe UGent, Michel Waroquier UGent and Veronique Van Speybroeck UGent (2010) JOURNAL OF ORGANIC CHEMISTRY. 75(3). p.885-896
abstract
The ring opening of 2-substituted N,N-dibenzylaziridinium ions by bromide is known to occur exclusively at the Substituted aziridine carbon atom via ail S(N)2 mechanism, whereas the opposite regioselectivity has been observed as the main pathway for ring opening by fluoride. Similarly, the hydride-induced ring opening of 2-substituted N,N-dibenzylaziridinium ions has been shown to take place solely at the less hindered position. To gain insight into the main factors causing this difference in regioselectivity, a thorough and detailed computational analysis was performed on the hydride- and halide-induced ring openings of l-benzyl-l-(alpha-(R)-methylbenzyl)-2(S)-(phenoxymethyl)aziridinium bromide. Intramolecular pi-pi stacking interactions in the aziridinium System were investigated at a range of levels that enable a proper description of dispersive interactions; a T-stacking conformer was found to be the most stable. Ring-opening mechanisms were investigated with it variety of DFT and high level ab initio methods to test the robustness of the energetics along the pathway in terms of the electronic level of theory. The necessity to utilize explicit solvent molecules to solvate halide ions was clearly shown; the potential energy surfaces for nonsolvated and solvated cases differed dramatically. It was shown that in the presence of a kinetically viable route, product distribution will be dictated by the energetically preferred pathway; this was observed in the case of hard nucleophiles (both hydride donors and fluoride). However, For the highly polarizable soft nucleophile (bromide), it was shown that in the absence of a large energy difference between transition states leading to competing pathways, the formation of the thermodynamic product is likely to be the driving force. Distortion/interaction analysis on the transition states has shown a considerable difference in interaction energies for the solvated fluoride case, pointing to the fact that sterics plays a major role in the outcome, whereas for the bromide this difference was insignificant, suggesting bromide is less influenced by the difference in sterics.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
LARGE MOLECULES, 3-DIPOLAR CYCLOADDITIONS, 1, DISPERSION CORRECTIONS, S(N)2 REACTIONS, BENZENE DIMER, THERMOCHEMICAL KINETICS, NONCOVALENT INTERACTIONS, DENSITY-FUNCTIONAL THEORY, POPULATION ANALYSIS, ASYMMETRIC-SYNTHESIS
journal title
JOURNAL OF ORGANIC CHEMISTRY
J. Org. Chem.
volume
75
issue
3
pages
885 - 896
Web of Science type
Article
Web of Science id
000273982900041
JCR category
CHEMISTRY, ORGANIC
JCR impact factor
4.002 (2010)
JCR rank
8/56 (2010)
JCR quartile
1 (2010)
ISSN
0022-3263
DOI
10.1021/jo902493w
project
HPC-UGent: the central High Performance Computing infrastructure of Ghent University
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
859207
handle
http://hdl.handle.net/1854/LU-859207
date created
2010-02-12 08:28:58
date last changed
2013-09-17 10:47:04
@article{859207,
  abstract     = {The ring opening of 2-substituted N,N-dibenzylaziridinium ions by bromide is known to occur exclusively at the Substituted aziridine carbon atom via ail S(N)2 mechanism, whereas the opposite regioselectivity has been observed as the main pathway for ring opening by fluoride. Similarly, the hydride-induced ring opening of 2-substituted N,N-dibenzylaziridinium ions has been shown to take place solely at the less hindered position. To gain insight into the main factors causing this difference in regioselectivity, a thorough and detailed computational analysis was performed on the hydride- and halide-induced ring openings of l-benzyl-l-(alpha-(R)-methylbenzyl)-2(S)-(phenoxymethyl)aziridinium bromide. Intramolecular pi-pi stacking interactions in the aziridinium System were investigated at a range of levels that enable a proper description of dispersive interactions; a T-stacking conformer was found to be the most stable. Ring-opening mechanisms were investigated with it variety of DFT and high level ab initio methods to test the robustness of the energetics along the pathway in terms of the electronic level of theory. The necessity to utilize explicit solvent molecules to solvate halide ions was clearly shown; the potential energy surfaces for nonsolvated and solvated cases differed dramatically. It was shown that in the presence of a kinetically viable route, product distribution will be dictated by the energetically preferred pathway; this was observed in the case of hard nucleophiles (both hydride donors and fluoride). However, For the highly polarizable soft nucleophile (bromide), it was shown that in the absence of a large energy difference between transition states leading to competing pathways, the formation of the thermodynamic product is likely to be the driving force. Distortion/interaction analysis on the transition states has shown a considerable difference in interaction energies for the solvated fluoride case, pointing to the fact that sterics plays a major role in the outcome, whereas for the bromide this difference was insignificant, suggesting bromide is less influenced by the difference in sterics.},
  author       = {Catak, Saron and D'hooghe, Matthias and De Kimpe, Norbert and Waroquier, Michel and Van Speybroeck, Veronique},
  issn         = {0022-3263},
  journal      = {JOURNAL OF ORGANIC CHEMISTRY},
  keyword      = {LARGE MOLECULES,3-DIPOLAR CYCLOADDITIONS,1,DISPERSION CORRECTIONS,S(N)2 REACTIONS,BENZENE DIMER,THERMOCHEMICAL KINETICS,NONCOVALENT INTERACTIONS,DENSITY-FUNCTIONAL THEORY,POPULATION ANALYSIS,ASYMMETRIC-SYNTHESIS},
  language     = {eng},
  number       = {3},
  pages        = {885--896},
  title        = {Intramolecular pi-pi stacking interactions in 2-substituted N,N-dibenzylaziridinium ions and their regioselectivity in nucleophilic ring-opening reactions},
  url          = {http://dx.doi.org/10.1021/jo902493w},
  volume       = {75},
  year         = {2010},
}

Chicago
Catak, Saron, Matthias D’hooghe, Norbert De Kimpe, Michel Waroquier, and Veronique Van Speybroeck. 2010. “Intramolecular Pi-pi Stacking Interactions in 2-substituted N,N-dibenzylaziridinium Ions and Their Regioselectivity in Nucleophilic Ring-opening Reactions.” Journal of Organic Chemistry 75 (3): 885–896.
APA
Catak, S., D’hooghe, M., De Kimpe, N., Waroquier, M., & Van Speybroeck, V. (2010). Intramolecular pi-pi stacking interactions in 2-substituted N,N-dibenzylaziridinium ions and their regioselectivity in nucleophilic ring-opening reactions. JOURNAL OF ORGANIC CHEMISTRY, 75(3), 885–896.
Vancouver
1.
Catak S, D’hooghe M, De Kimpe N, Waroquier M, Van Speybroeck V. Intramolecular pi-pi stacking interactions in 2-substituted N,N-dibenzylaziridinium ions and their regioselectivity in nucleophilic ring-opening reactions. JOURNAL OF ORGANIC CHEMISTRY. 2010;75(3):885–96.
MLA
Catak, Saron, Matthias D’hooghe, Norbert De Kimpe, et al. “Intramolecular Pi-pi Stacking Interactions in 2-substituted N,N-dibenzylaziridinium Ions and Their Regioselectivity in Nucleophilic Ring-opening Reactions.” JOURNAL OF ORGANIC CHEMISTRY 75.3 (2010): 885–896. Print.