Skip to main content

Research Repository

Advanced Search

The Role of the Fused Ring in Bicyclic Triazolium Organocatalysts: Kinetic, X-ray, and DFT Insights

Zhu, Jiayun; Moreno, Inmaculada; Quinn, Peter; Yufit, Dmitry S.; Song, Lijuan; Young, Claire M.; Duan, Zhuan; Tyler, Andrew R.; Waddell, Paul G.; Hall, Michael J.; Probert, Michael R.; Smith, Andrew D.; O’Donoghue, AnnMarie C.

The Role of the Fused Ring in Bicyclic Triazolium Organocatalysts: Kinetic, X-ray, and DFT Insights Thumbnail


Authors

Jiayun Zhu jiayun.zhu@durham.ac.uk
PGR Student Doctor of Philosophy

Inmaculada Moreno

Peter Quinn

Lijuan Song

Claire M. Young

Zhuan Duan

Andrew R. Tyler

Paul G. Waddell

Michael J. Hall

Michael R. Probert

Andrew D. Smith



Abstract

Bicyclic triazolium scaffolds are widely employed in N-heterocyclic carbene (NHC) organocatalysis. While the incorporation of a fused ring was initially for synthetic utility in accessing chiral, modular triazolyl scaffolds, recent results highlight the potential for impact upon reaction outcome with the underpinning origins unclear. The common first step to all triazolium-catalyzed transformations is C(3)-H deprotonation to form the triazolylidene NHC. Herein, we report an analysis of the impact of size of the fused (5-, 6-, and 7-membered, n = 1, 2, and 3, respectively) ring on the C(3) proton transfer reactions of a series of bicyclic triazolium salts. Rate constants for the deuteroxide-catalyzed C(3)-H/D-exchange of triazolium salts, kDO, were significantly influenced by the size of the adjacent fused ring, with the kinetic acidity trend, or protofugalities, following the order kDO (n = 1) > kDO (n = 2) ≈ kDO (n = 3). Detailed analyses of X-ray diffraction (XRD) data for 20 triazolium salts (including 16 new structures) and of computational data for the corresponding triazolylidene NHCs provide insight on structural effects of alteration of fused ring size. In particular, changes in internal triazolyl NCN angle and positioning of the most proximal CH2 with variation in fused ring size are proposed to influence the experimental protofugality order.

Citation

Zhu, J., Moreno, I., Quinn, P., Yufit, D. S., Song, L., Young, C. M., Duan, Z., Tyler, A. R., Waddell, P. G., Hall, M. J., Probert, M. R., Smith, A. D., & O’Donoghue, A. C. (2022). The Role of the Fused Ring in Bicyclic Triazolium Organocatalysts: Kinetic, X-ray, and DFT Insights. Journal of Organic Chemistry, 87(6), 4241-4253. https://doi.org/10.1021/acs.joc.1c03073

Journal Article Type Article
Online Publication Date Mar 1, 2022
Publication Date 2022
Deposit Date May 25, 2022
Publicly Available Date May 26, 2022
Journal Journal of Organic Chemistry
Print ISSN 0022-3263
Electronic ISSN 1520-6904
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 87
Issue 6
Pages 4241-4253
DOI https://doi.org/10.1021/acs.joc.1c03073
Public URL https://durham-repository.worktribe.com/output/1204783

Files

Published Journal Article (2 Mb)
PDF

Publisher Licence URL
http://creativecommons.org/licenses/by/4.0/

Copyright Statement
Open Access. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0), which permits any use, distribution and reproduction in any medium, provided the original author(s) and source are credited






You might also like



Downloadable Citations