Issue 31, 2022

Back electron transfer rates determine the photoreactivity of donor–acceptor stilbene complexes in a macrocyclic host

Abstract

Host–guest 2 : 1 complexation of photoreactive alkene guests improves the selectivity of [2 + 2] photodimerizations by templating alkene orientation prior to irradiation. Host–guest chemistry can also provide 1 : 1 : 1 complexes through the inclusion of electronically complementary donor and acceptor guests, but the photoreactivity of such complexes has not been investigated. We imagined that such complexes could enable selective cross-[2 + 2] photocycloadditions between donor and acceptor stilbenes. In pursuit of this strategy, we investigated a series of stilbenes and found 1 : 1 : 1 complexes with cucurbit[8]uril that exhibited charge-transfer (CT) absorption bands in the visible and near-IR regions. Irradiation of the CT band of an azastilbene, 4,4′-stilbenedicarboxylate, and cucurbit[8]uril ternary complex led to a selective cross-[2 + 2] photocycloaddition, while other substrate pairs exhibited no productive chemistry upon CT excitation. Using transient absorption spectroscopy, we were able to understand the variable photoreactivity of different stilbene donor–acceptor complexes. We found that back electron transfer following CT excitation of the photoreactive complex is positioned deep in the Marcus inverted region due to electrostatic stabilization of the ground state, allowing [2 + 2] to effectively compete with this relaxation pathway. Control reactions revealed that the cucurbit[8]uril host not only serves to template the reaction from the ground state, but also protects the long-lived radical ions formed by CT from side reactions. This protective role of the host suggests that donor–acceptor host–guest ternary complexes could be used to improve existing CT-initiated photochemistry or access new reactivity.

Graphical abstract: Back electron transfer rates determine the photoreactivity of donor–acceptor stilbene complexes in a macrocyclic host

  • This article is part of the themed collection: New Talent

Supplementary files

Article information

Article type
Paper
Submitted
10 3月 2022
Accepted
06 4月 2022
First published
06 4月 2022

Org. Biomol. Chem., 2022,20, 6201-6210

Author version available

Back electron transfer rates determine the photoreactivity of donor–acceptor stilbene complexes in a macrocyclic host

C. T. Eckdahl, C. Ou, S. Padgaonkar, M. C. Hersam, E. A. Weiss and J. A. Kalow, Org. Biomol. Chem., 2022, 20, 6201 DOI: 10.1039/D2OB00472K

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