Issue 16, 2021

Perylene bisimide cyclophanes as receptors for planar transition structures – catalysis of stereoinversions by shape-complementarity and noncovalent π–π interactions

Abstract

Perylene bisimide (PBI) cyclophanes have been shown to form ideal hosts for large aromatic molecules, offering rigid cavities and ideal monomer spacing for π–π stacking interactions between the host and guest. Here, we show computationally that these characteristics also make PBI cyclophanes ideal receptors for the planar transition structures of a number of representative stereoinversion processes. The observed catalytic effect can hereby be explained using two fundamental concepts: transition state stabilization due to shape-complementarity between cyclophane and the transition structures and, to a smaller extent, ground state destabilization due to non-complementarity between cyclophane and equilibrium structures. Energy decomposition analyses of the noncovalent interactions between the host and guest structures reveal that dispersion and electrostatic interactions make the largest contributions to stabilizations and thus suggest that catalysis in this system is mainly driven by π–π stacking interactions.

Graphical abstract: Perylene bisimide cyclophanes as receptors for planar transition structures – catalysis of stereoinversions by shape-complementarity and noncovalent π–π interactions

Supplementary files

Article information

Article type
Research Article
Submitted
14 Mai 2021
Accepted
09 Jun 2021
First published
10 Jun 2021

Org. Chem. Front., 2021,8, 4408-4418

Perylene bisimide cyclophanes as receptors for planar transition structures – catalysis of stereoinversions by shape-complementarity and noncovalent π–π interactions

A. A. Kroeger and A. Karton, Org. Chem. Front., 2021, 8, 4408 DOI: 10.1039/D1QO00755F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements