Synthesis and photoinduced switching properties of C<sub>7</sub>-heteroatom containing push–pull norbornadiene derivatives

We report the synthesis and characterization of heteroatom-incorporated norbornadiene (NBD) derivatives. Push-pull substitution on the 2 and 3 position as well as introduction of oxygen or nitrogen at position 7 of the NBD scaffold have led to the development of a new family of photoswitches. We studied the potential conversion of norbornadiene to quadricyclane (QC) isomers. As main investigation tools, UV-vis and NMR spectroscopy were utilized. We determined significant spectral features of the formed NBD species, including λ<sub>max</sub> and λ<sub>onset</sub> values, all of which exhibit redshifts compared to their isocyclic counterparts. Additionally, the selected QC isomers were subjected to thermal and catalytic back-conversion studies.

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Publication Details

Journal
Beilstein Journal of Organic Chemistry
Published
2025-04-22
DOI
https://doi.org/10.3762/bjoc.21.64
Citations
1
Primary Topic
Photochromic and Fluorescence Chemistry
Type
article
Field-Weighted Citation Impact
0.52
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article

Synthesis and photoinduced switching properties of C7-heteroatom containing push–pull norbornadiene derivatives

Andreas Hirsch, Daniel Krappmann
1 citations
Beilstein Journal of Organic Chemistry
Photochromic and Fluorescence Chemistry
0.52
article

Synthesis and photoinduced switching properties of C7-heteroatom containing push–pull norbornadiene derivatives

Andreas Hirsch, Daniel Krappmann
article en
1 citations

Abstract

We report the synthesis and characterization of heteroatom-incorporated norbornadiene (NBD) derivatives. Push-pull substitution on the 2 and 3 position as well as introduction of oxygen or nitrogen at position 7 of the NBD scaffold have led to the development of a new family of photoswitches. We studied the potential conversion of norbornadiene to quadricyclane (QC) isomers. As main investigation tools, UV-vis and NMR spectroscopy were utilized. We determined significant spectral features of the formed NBD species, including λ<sub>max</sub> and λ<sub>onset</sub> values, all of which exhibit redshifts compared to their isocyclic counterparts. Additionally, the selected QC isomers were subjected to thermal and catalytic back-conversion studies.

Beilstein Journal of Organic ChemistryVol. 21
Friedrich-Alexander-Universität Erlangen-Nürnberg (DE)
Life in Land
Openalex Percentile: Top 40%
Photochromic and Fluorescence Chemistry
0.52
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Synthesis and photoinduced switching properties of C<sub>7</sub>-heteroatom containing push–pull norbornadiene derivatives — Andreas Hirsch, Daniel Krappmann · Beilstein Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS